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QA Manager (Univercells)

UNIVERCELLS recherche un(e)

 

QA Manager

 

Based in Nivelles (Belgium), you will join a collaborative team of passionate change-makers.

YOUR MISSION: you will define and implement the QA strategy and tactical execution for Univercells Technologies. You will report directly to the COO of Univercells Technologies and maintain a dotted line reporting relationship to the Chief Quality Officer of Univercells, the holding organization.

RESPONSIBILITIES

  • You will oversee all quality activities in the Univercells Technologies organization
  • You will build, lead, coach and develop the QA team and organization. You will also evaluate and improve the current QA process and provide training when necessary
  • You will continue to develop and maintain a comprehensive Quality Management System and tools and you will lead, develop and implement global quality strategies to ensure that R&D and production activities (drugs or equipment) will comply with all quality requirements in key markets
  • You will maintain development, product and processes quality by enforcing quality assurance policies and procedures
  • You will collaborate with other members of management to disseminate quality mindset throughout the company.
  • You will help balance the quality needs of our customers and partners with the needs of the business using a pragmatic problem-solving approach.
  • You will participate in inspections, audits, and certifications
  • You will manage the Univercells technologies Quality budget
  • You will provide adequate QA/QMS reporting

 

QUALIFICATIONS

  • MSc in Life Sciences or (Bio) Engineering
  • Minimum 8 years combined experience in QA in Pharma/Biotech, preferably from the supply base to bio-pharma producers (such as equipment, consumables)
  • Strong management and leadership, as well as influential skills.
  • Proven track record in Quality Management System implementation
  • GxP knowledge
  • Experience with audit and certifications
  • Strong in communication skills and team player
  • Ability to work in fast-paced environments and to combine helicopter view and tactical actions
  • Fluent English, French is an asset.

 

OFFER

We offer a long-term contract (CDI), a competitive salary package (health insurance, company car, pension plan, meal vouchers…) and the possibility of evolution in an international, dynamic and fast-growing company.

Don’t hesitate: apply now!

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Offres d'emplois

Product Change Manager (IBA)

 

IBA recherche un(e)

 

Product Change Manager

 

As Product Change Manager in the Proteus Product Management team, you are the interface between the “Scouts” reporting product non-conformities and/or change requests and the Project Manager in charge of the development and deployment of the solutions.

You Are Accountable For

  • Ensuring that the product changes are managed in a controlled and efficient way, according to the relevant processes.
  • Making sure that the product change requests are aligned with the product strategy, the business priorities and the regulation.
  • Leading the Decision Change Control Board, recording and sharing decisions on product changes.
  • Optimizing the costs by packaging the product change requests considering the impacts, the risks, the target configurations and the available capacity and expertise.
  • Defining the applicability of the changes and clarifying the deployment strategy, in agreement with the “Scouts” and the Project Managers in charge of the deployment of the solutions.
  • Making sure that product changes are implemented and deployed as decided, in the expected timeframe and costs.
  • Providing related records and indicators.
  • Communicating decisions and ensuring feedback to the “Scouts”.

 

Profile

 

  • You have a Master degree in Engineering (e.g. computer science, electronics, mechanics) or an equivalent experience.
  • You have at least 3 years of experience in Project or Product management.

 

You Are

  • You are an assertive person with strong interpersonal skills, able to drive change.
  • You are a flexible, stress resistant and rigorous person with very good organizing skills and able to set priorities and to make decisions.
  • You are a client minded person with excellent communication skills both in French and in English.

 

Company

IBA is a cancer diagnostics and treatment company and the worldwide technology leader in the field of proton therapy. The Company’s expertise lies in the development of next generation proton therapy technologies and radiopharmaceuticals that provide oncology care providers with premium quality services and equipment, including IBA’s leading fully integrated IntegraLab® radiopharmacy system, and Dosimetry advanced solutions for Quality Assurance of medical equipment and increased patient safety.

Headquartered in Belgium and employing more than 1,500 people worldwide, IBA currently has installed systems across Europe and the US and is expanding into emerging markets.
The Company is focused on providing solutions in the fight against cancer.
Belgium

Offer

If you are stimulated by multicultural challenges, we offer you the opportunity to join a team of more than 40 nationalities working on more than 45 different sites on 3 continents.

IBA offers you a competitive performance based compensation package and a flexible work environment. You have real possibilities to evolve within IBA’s worldwide, leading organization and to create your own career path, supported by training programs to acquire new skills and ensure they stay sharp.

As an Equal Opportunity Employer IBA is committed to a diverse workforce.

Pour postuler, c’est ici.

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Offres d'emplois

Electronic Design Engineer (EVS)

EVS Broadcast Equipment (Liège) recherche un(e)

 

Electronic Design Engineer

The candidate will join the EVS electronic design team. He/she will contribute to the development of new electronic hardwares, mainly in the design of FPGA code.

He will ensure the robustness, reliability, and testability of its implementations. Taking advantage of his/her experience, he/she will contribute with the other team members to the different steps of the development process: analysis, technical specification, design, components selection, development, testing, technical documentation, and maintenance.

The Electronic Design Engineer is able to work closely with peers in a fast-paced dynamic environment.

 

Job Description

  • Analyze and review product requirements, and discuss technical feasibility
  • Study of the related technologies and tools
  • Build technical design proposals
  • Design of the FPGA code in Verilog and/or VHDL language
  • Participate in peer code reviews
  • Software simulation and verification
  • Design of a test and debug environment that can also be used for the production quality control
  • Debug of the code on the real final hardware platform
  • Create or maintain technical documentation
  • Support EVS software developers that will integrate the new hardware
  • Solve defects reported in the defect tracking system
  • Maintain existing code
  • Identify risks and discuss them with the Quality Control department for building adequate test plans
  • Make work estimates for the tasks assigned to you
  • Plan, track and report your daily work and your assigned tasks to your direct manager
  • Follow the EVS software development process (Source Control Management, Defect Tracking, Coding Rules, Continuous Integration)
  • Identify and propose process improvements

 

Profile

Engineer, Master’s or Ph.D. degree in Electronic or equivalent by experience

The following technical experiences are not mandatory, and will be considered as an asset:

  • Experience with Altera or Xilinx FPGA components is an asset
  • Experience with HD/SD video format and interfaces, SMPTE standards is an asset
  • Experience with SDR, DDR, DDR2, DDR3 components is an asset
  • Experience with video compression (JPEG, MPEG, H264, AVCI, ProRes, DNx, …) is an asset
  • Experience with PCI and PCIe is an asset
  • Experience with Ethernet, IP, UDP, TCP, streaming protocols is an asset
  • Experience with Altera Quartus, Modelsim is an asset
  • Experience in C/C++ is an asset
  • Experience in embedded software development (firmware) is an asset
  • Experience with both Linux and/or Windows OS is an asset
  • Experience in multithreading, robotics and/or real-time environments is an asset
  • Experience in the broadcast industry is an asset
  • Experience in Agile / Scrum development practices is an asset

 

Soft skills:

  • Achieves high-quality results through thoughtful analysis and planning; target driven and result oriented
  • Excellent analytical skills, strong object-oriented design skills
  • Focus on quality, detail minded, willing to take care of customer point of view
  • Open for changes and continuous learning
  • Capable of executing tasks autonomously, of planning and communicating planning and progress, of getting help where needed
  • Shows initiative, is curious and communicates well about initiatives
  • Good written and verbal communication skills, shares information actively; responds properly, reports on-time; accepts criticism and other opinions, addresses criticism constructively
  • Excellent team player
  • High-stress resistance; does not give up in a crisis situation; does not lose control under pressure

 

Languages

Fluent in French and working knowledge of English

Offer

You will benefit from working in a friendly, lively environment having ambitious commercial objectives. Our dynamic and young team brings the best out of motivated potentials. In addition, you will receive a competitive salary and a range of other employee benefits.

 

Pour postuler, c’est ici.

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Offres d'emplois

Industrialization Scientist (M/F) – Celyad

Celyad recherche un(e)

 

Industrialization Scientist (M/F)

 

 

The successful candidate will be based in Mont-Saint-Guibert (Belgium) and will report into the Industrialization Director.

Role :

Support the team’s efforts to adapt and optimize the base R&D CAR-T production processes to GMP manufacturing and commercial production.

Responsibilities :

  • Design and oversee process research studies (incl. protocol writing, working closely with technicians, data analysis and report writing);
  • Coordinate study planning and execution from the Industrialization group with R&D, QC and manufacturing teams;
  • Evaluate new and alternative raw materials and establish raw material specifications in collaboration with QA and QC;
  • Contribute to Process Qualifications studies and comparability studies;
  • Present data to project group and larger multidisciplinary teams including externally at meetings/congresses/conferences as appropriate;
  • Execute research timelines to meet program and corporate objectives.

 

Qualifications & Experience :

  • PhD in cell biology or related field;
  • Minimal 3 years post-doctoral or research experience in academia or industry;
  • Expertise with small and large-scale mammalian cell culture, preferably T-cells, and experience with closed culture systems and cell processing equipment and techniques;
  • Previous experience with cellular characterization assays including techniques such as, multiple parameter flow cytometry, ELISA’s, and molecular biology experience is required;
  • Experience with Good Manufacturing Practices (cGMP);
  • Experience with writing protocols and reports.

 

Skills & Competencies :

  • Demonstrated ability to work collaboratively across team functions to achieve project objectives on schedule;
  • Demonstrated ability to work both independently and within a goal-oriented team;
  • Excellent communication skills (both written and oral), time management, record keeping and data analysis skills;
  • Languages: fluency (written & spoken) in English & French, additional languages are a plus;
  • Hands on personality and passion for bringing operational value to the organization;
  • Patience, resilience and strong goal-oriented mindset;
  • High level of autonomy and initiative.

 

For more information about this position or about the Company, please contact us by email at job@celyad.com

 

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Offres d'emplois

Scientist Liquid Chromatography & Mass Spectrometry – Technical R&D

GSK (Rixensart) recherche un(e)

 

Scientist Liquid Chromatography & Mass Spectrometry – Technical R&D

 

Role

The role of the In-Process Analytics team within the Drug Substance organization is three-fold

The Belgian In-Process Analytics (IPA) team for Vaccine Drug Substance (VDS) is actively looking for a Scientist with a solid expertise in Immunoassays.

  • To Develop fit for purpose methods/assays aimed to support process development activities and ultimately contribute to the process design selection/evaluation/characterization.
  • To Identify novel or consolidate analytical capabilities of the organization for vaccine development.
  • To Characterize/quantitate product antigens/Virus like particles or to identify and quantitate process-related impurities and develop assays to monitor process performance.

 

Our activities are covering a wide variety of processes (Fermentation, Cell culture, Viral production, purification, coupling) at different development stages (early to late development, Life Cycle).

Your Responsibilities

As a Scientist within the IPA group, you will integrate with a multidisciplinary team and you will be in close contact with experts in various analytical technologies (HPLC, Flow Cytometry, Immunoassays, Spectrophotometry, Process Analytical).

Your mission will be focused on the development of Proteomics assays to support our Upstream/Downstream Process development colleagues in different research/development contexts (process development, process understanding, troubleshooting, Life cycle…).

In addition, you will contribute to the establishment of our new High Throughput cell based assay platform aimed to automate and reduce our development timelines.

  • You will contribute to the development and implementation of Proteomics assays (LC-MS label free, MALDI-Tof,…) to support VDS development activities.
  • You will write the documentation associated to the development activities (development reports, protocols)
  • You will train and supervise technicians/scientists in Proteomics.
  • You will represent IPA-VDS internally (Preclinical and Technical R&D) and collaborate proactively with our preclinical and/or analytical method development colleagues.
  • You will develop other analytical methods as needed.

 

Why you?

Basic Qualifications

We are looking for professionals with these required skills to achieve our goals:

  • PhD in life science or equivalent experience with a solid experience in Proteomics and its package of associated tools (BioTools, Mascot, Peaks, …).
  • Excellent writing and communication skills.
  • As the group is a multidisciplinary organization, the willingness to develop beyond the initial expertise is a prerequisite to apply to this position.
  • English & French are a must, other languages a plus.
  • Analytical mind-set.

 

Preferred Qualifications

If you have the following characteristics, it would be a plus:

  • Experience in High Throughput technologies is an asset (eg. Liquid Handling systems such TECAN).
  • Be curious.
  • Be flexible and have the capacity to work with priorities.
  • Have the capacity to work and communicate transversally and not in a silo environment.

 

Why GSK?

Our values and expectations are at the heart of everything we do and form an important part of our culture.

These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork in a culture of Innovation, Performance and Trust.

GSK Vaccines – Our Vaccines business has a broad portfolio and innovative pipeline of vaccines to protect people of all ages. We deliver over two million vaccine doses per day to people living in over 160 countries.

For further information, please visit www.gsk.com.

Our Department

Patient-focused Research and Development (R&D) is the heart of our business. Our R&D department seeks to discover and develop new vaccines, to protect against diseases where vaccines are not yet available and to improve on those vaccines that already exist. Part of our R&D programme targets diseases particularly prevalent in the developing world, including the World Health Organisation’s three priority diseases – HIV/AIDS, tuberculosis and malaria. Research into candidate vaccines for other diseases of the developing world, such as dengue are at an earlier stage of development.

When it comes to developing the vaccines of the future, we’re looking for real experts in their respective fields who are interested in working in the stimulating environment of an international healthcare company.

We emphasise the value of teamwork and we look for people ready to share our values of transparency, respect, integrity and patient focus.

At GSK we value diversity and treat all candidates equally. We aim to create an inclusive workplace where all employees feel engaged, supportive of one another, and know their work makes an important contribution.

We provide a supportive working environment, and a range of development challenges and opportunities. We also offer competitive benefits and compensation packages designed to attract and to retain the very best.

If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing.

Pour postuler, c’est ici.

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Offres d'emplois

Senior Director, R&D Procurement – Medical & Regulatory

GSK recherche un(e)

 

Senior Director, R&D Procurement – Medical & Regulatory

GSK is actively recruiting for a transformative and highly-visible R&D Procurement – Medical and Regulatory leader to build an expanded sourcing and contract management capability to support GSK’s global Pharma, Vaccines, and Consumer Health global R&D priorities.

This role will be accountable for all sourcing and contracting across GSK’s Medical and Regulatory categories (e.g. Evidence Generation, Medical Communications/Publications, Regulatory, Safety/Pharmacovigilance, etc.).

This will include alignment with the key GSK leaders responsible for these services across both R&D and Commercial, the development and implementation of category strategies, the contracting for master/service agreements within the categories, the simplification of relevant processes, the management of supplier relationships that fall outside of the enterprise SRM structure for these categories, and for ensuring these medical and regulatory suppliers commit to deliver GSK’s performance/quality/financial requirements.

These Responsibilities Include Some Of The Following

This role will provide YOU the opportunity to lead key activities to progress YOUR career.

  • Manage the category globally; creating comprehensive global sourcing, contracting, and supplier relationship management strategies for the relevant categories.
  • Role model GSK values and behaviors, foster the environment of a modern employer, engage talent, develop capabilities, promote GSK network/brand, and consistently demonstrate professional behaviors.
  • Deliver cultural change to enable an organization focused on decision-making accountability, quality, speed, performance, results, and collaboration.
  • Develop leaders, at all levels of the organization to encourage open and transparent communications, develop and rotate our talent, and demonstrate GSK’s values and expectations daily.
  • Ensure clarity of roles/job descriptions, expectations/objectives, and development plans for all team members.
  • Develop, optimize, and deliver a strategy for most efficient contracting and buy-channel within relevant categories.
  • Ensure Master and service-level agreements are strategically aligned with R&D Business goals
  • For select suppliers, establish and manage SRM structure aligned with broader R&D Procurement SRM structure.
  • Build strategic relationships with a network of senior GSK global stakeholders to understand business requirements, identify opportunities to create value and to position Procurement’s value proposition, and align sourcing strategies accordingly.

 

Create compelling business cases for change and obtain support to execute from senior GSK leaders across R&D, Finance, HR, etc.; agree how benefits will be achieved and accounted for.

  • Deliver global benefits identified in strategies through effective strategy execution aligned to assurance of supply (risk management), compliance, quality, service, cost and innovation.
  • Engage all relevant stakeholders in the sourcing strategy and contract management activities to ensure GSK requirements are contracted and delivered.
  • Build strategic relationships with leaders of key suppliers to ensure the value of the supplier-GSK relationship is optimized; account for cross-GSK requirements in supplier relationships and leverage business review meeting process to drive the relationship.
  • Build the organizational capabilities necessary to implement GSK strategy, now and in the future.
  • Ensure appropriate communication strategy is in place and in use within the relevant Procurement and GSK networks.

 

Why you?

Basic Qualifications

  • Experience working closely with senior Medical and Regulatory leaders.
  • Experience leading a global team; experience initiating and implementing simplification and change.
  • A demonstrated ability to solve complex category and supplier challenges.
  • Experience influencing and matrix-managing peers as a member of an R&D procurement leadership team.

 

Preferred Qualifications

A relevant advanced degree (MS, MBA, JD, etc.) is preferred.

Why GSK?

Our values and expectations are at the heart of everything we do and form an important part of our culture.

As GSK Focuses On Our Values And Expectations And a Culture Of Innovation, Performance, And Trust, The Successful Candidate Will Demonstrate The Following Capabilities

These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork.

  • Agile and distributed decision-making – using evidence and applying judgement to balance pace, rigor and risk, governance and control, managing ambiguity and paradox.
  • Managing individual performance.
  • Creating a performance culture and driving results, prioritization, execution, delivering performance.
  • Setting strategic direction and leading on-going organisational transformation.
  • Building a resilient organisation.
  • Building strong relationships and collaboration in service of common goals, engaging the organisation and building trusted external networks for mutual benefit.
  • Managing P&L and capital allocation.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).

GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

 

Pour postuler, c’est ici.

 

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Offres d'emplois

Back-end Developer (OncoDna)

OncoDNA recherche un(e)

 

Back-end Developer

OncoDNA helps oncologists to choose the most appropriate treatment for each patient’s cancer profile. In addition to diagnostic tests, OncoDNA has developed a data interpretation platform (SaaS model) for cancer centres. OncoDNA is one of the European leaders in the field of precision medicine. The company is based in the Gosselies Biopark and employs 45 people in four countries.

As part of its growth, OncoDNA is looking for a back-end developer to join the IT Team

As a back-end developer, you grab business requirements understand how they impact the back-end engines, describe the system requirements, and design solutions in collaboration with the architect. Once designs have been validated, implement the solution, including the related unit tests, and transfer knowledge to Front-end developers.

All in all, back-end engines shall be capable of both handling front-end demands and integrate with partners’ own systems.

Under IT Director’s responsibility, you …

Collaborate in the development of back-end IT systems that are embedded into OncoDNA’s product offering:

  • Analyze business’ demand and regulatory (mainly data privacy) constraints; helping business stakeholders to clarify (when needed) their expectations
  • Participate in various SCRUM ceremonies together with the rest of the team
  • Use (and improve) best practices and standards
  • Respect architecture vision … and propose evolutions
  • Code with Python within the various frameworks chosen by the team … propose improvement to those framework and support migration
  • Be responsible for timeline and quality

 

Systematically follow the work items in structured ticketing and Project management system (JIRA stack)

Actively support the evolution of the application landscape by

• Keeping in touch with technology evolution and propose introduction of new tools and frameworks

• Being creative and participating in the innovation activities of the company

 

Your profile

  • You have a master in computer science or equivalent
  • You are stress resistant
  • You have a good knowledge of OO languages (Python) and Data(Science)-related frameworks
  • You are experienced in designing, documenting and respecting coding best practices
  • You are experienced in conceptualizing and documenting designs
  • You are able to work with a Team
  • You are experienced with SCRUM (or other agile framework) is an asset
  • You are focus on customer satisfaction – quality driven
  • You get solid understanding of data analysis, as well as solid scientific background in general and a solid understanding of Information Technology and Data Science
  • You are fluent in English (oral & written), a second European language is an asset.

 

We offer you

  • An opportunity to participate in the evolution of tomorrow’s medicine
  • A young, dynamic and involved team in the fight against cancer
  • A challenging position within a dynamic and growing company
  • A possibility to play a key role in the company’s scale-up phase
  • An international environment in a rapidly changing digital industry
  • An attractive package commensurate with the position, responsibilities and its context

 

About

At OncoDNA we strive to help cancer patients. OncoDNA offers solutions combining the most relevant molecular technologies in order to provide a comprehensive characterization of the patient’s cancer, hence supporting oncologists in their treatment and follow-up decisions.

 

Interesting to join our team ?

Don’t hesitate to apply via jobs@oncodna.com.

 

 

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Offres d'emplois

Process Engineer (CooperVision)

CooperVision (Liège) recherche un(e)

 

Process Engineer

CooperVision®, Inc., a unit of The Cooper Companies, Inc. (NYSE: COO), is one of the world’s leading manufacturers of soft contact lenses. The Company produces a full array of monthly, two-week and daily disposable contact lenses, all featuring advanced materials and optics. CooperVision has a strong heritage of solving the toughest vision challenges; such as astigmatism, presbyopia and ocular dryness; and offers the most complete collection of spherical, toric and multifocal products available.

Through a combination of innovative products and focused practitioner support, the company brings a refreshing perspective to the marketplace, thereby creating real advantages for customers and wearers.

From our extensive network of facilities in 12 countries across five continents, CooperVision distributes high-quality lenses virtually everywhere contact lenses are worn.

 

Job Summary

  • Responsible for the investigation, get the best use of the infrastructure, development and delivery of advanced automation technology. Introducing new or improving existing equipment and processes to reduce costs, improve quality, increase capacity, to support the business requirements of Distribution Operations.
  • Provide high level technical expertise to the business from the onset of project initiation through post implementation. Overseeing project budget and timeline, securing necessary resources and driving projects to completion.
  • Organizes and oversees the collection and analysis of pertinent data.
  • Leads and participates in process validations to assure compliance with company specifications to include internal quality systems and external regulations (MDSAP).
  • Provides input to management to support the development and application of current/new business processes.

 

Essential Functions & Accountabilities

 Appraise, specify, develop, commission and test new and existing production automated systems and equipment

 Lead the selection of automated equipment, vendors and development of the best vendors to meet business requirements

 Lead, deliver and implement new technology projects that meet time, cost and quality targets, delivering new, validated, robust and commercially beneficial processes

 Design, develop with vendors, and supervise all aspects of process control systems, equipment, and machinery

 Support of Programmable Logic Controls (PLCs) based hardware and software

 Conduct equipment and process safety compliance assessments, appraisals, capability studies and validation/verification programs in accordance with MDSAP and medical device regulatory requirements and provide significant technical contribution to projects

 Is recognized internally as an advanced practitioner of their technical skills and a good team player

 Manages projects of high complexity, including budgets and resources (internal and external), if appropriate

 Participate in global multi-functional project teams as an expert/module leader to ensure the effective delivery of business objectives

 Leads equipment purchases and redesigns, including developing User Requirements Specifications (URS), conducting Factory and Site Acceptance Testing (FAT and SAT), and coordinating activities with vendors

 Leads engineering changes, writes Engineering Change Orders (ECOs), and documents changes appropriately in eQMS system in collaboration with QA team

 If necessary, approval and management for all regulatory documentation, such as qualification protocols and specifications.

 Reports on projects to EHS & Facility & maintenance Manager and project team involved

 Share and adhere to Lean philosophy et collaborate with Lean department to Apply Lean Six Sigma tools to projects, processes and procedures to maximize equipment reliability and efficiency

 Assists when necessary in investigating instances of nonconformance and facilitates the determination of root cause and corrective/preventative action

 Develops SOP’s, work instructions, and other quick reference material as needed

 Work in active collaboration with maintenance team and support maintenance activities when necessary

 Interact positively with the WMS team to perform the ongoing projects

 

Qualifications

Knowledge, Skills and Abilities: Technical Skills

  • Excellent understanding of distribution environments and equipment testing
  • Ability to apply sound problem-solving skills using technical risk assessment and analytical skills
  • Solid Works or/and AutoCAD knowledge is an asset
  • Knowledge of motion control, robotics, bar code readers
  • Linux, Visual Studio, and Visual Basic knowledge is an asset
  • Knowledge of MDSAP/medical packaging regulations and protocols is preferred
  • Knowledge with multiple automation system platforms including PLC, SCADA and other applicable systems is an asset
  • Generic Skills
  • Fluent in French and English

 

Behavioral Skills

  • Excellent interpersonal skills and ability to interact with all levels of organization
  • Able to work without supervision.
  • Strong planning and decision-making capabilities
  • Sensitized and able to promote EHS culture
  • Excellent written, presentation and verbal communications skills
  • Intrinsically motivated and pro-active in the searching and awareness of new technology
  • Ability to work closely and effectively with other company disciplines as well as outside vendors and organizations to achieve company goals

 

Work Environment:

  • Normal warehouse and office environment.
  • Flexibility with working hours.
  • Availability for international travel punctually

 

Experience:

  • 2-3 years of experience as an Engineer in an operational environment
  • Background in mechanics, electricity, automation, distribution methods, and ideally with printing and verification processes
  • Project management experience in machinery
  • Experience in distribution/logistics environment is preferred
  • Automated manufacturing technology experience is an asset

 

Education:

Master’s Degree in Industrial Engineering

 

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Offres d'emplois

R&D Engineer (Carmeuse)

Carmeuse (Ottignies-Louvain-la-Neuve) recherche un(e)

 

R&D Engineer

Job Description

  • Developing breakthrough products and processes
  • Continuously improving and consolidating the scientific and technical knowledge related to Carmeuse’s products and processes
  • Supporting our operation or our customers in the implementation of new solutions
  • Providing scientific and technical advice to all functional and operational departments

 

Main Responsibilities

  • Contribute to R&D projects in collaboration with academic and industrials partners
  • Plan and follow laboratory, pilot and industrial trials
  • Design and operate pilot-scale units
  • Analyse, interpret test results and write scientific reports
  • Perform process simulation and mathematical modeling
  • Watch scientific/technical literature and participate in international conferences
  • Apply creative thinking, analysis and good judgement to propose innovative concepts, new products and new processes

 

Ideal Candidate

Education: Master or doctorate degree in Chemistry, Chemical Engineering, Materials Sciences, Gas Technology, Environmental Sciences or equivalent.

Experience:Some years of experience in R&D, production, process or product development will be considered as valuable professional

 

Soft skills:

Creative, curious and passionate , Autonomous , Excellent networking skills , Team work , Excellent communication skills , Agility

 

Professional skills:

French and English (written & spoken)

This role will have internal and external interactions, mainly with External Industrial Partners, Universities and Research Centers, Customers, Equipment Providers, Administrations and Industry Associations…

 

About Us

Carmeuse started out as a small family-run business in Belgium.

Today it’s a leading global producer of lime, high calcium limestone and dolomitic stone. Its products are essential to energy producers, environmental services, construction and manufacturing.

With over 90 production facilities spread across almost every continent, and over 4,500 employees working at Carmeuse every day, the company’s most treasured resources are its people.

 

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Offres d'emplois

Software Engineer (Unisensor)

Unisensor (Ougrée) recherche un(e)

 

 

Software Engineer

 

For more than 20 years, Unisensor has been a pioneer in diagnostic engineering by developing rapid testing solutions for food safety.

To continue our expansion, we are looking for a SOFTWARE ENGINEER.

Are you excited about picking up this role in a rapidly growing company, working within a dynamic human size team with great ambitions?

1. Role and responsibilities

The Software Engineer is responsible for building, enhancing and maintaining connected devices and/or systems. You will work on analysis equipment sold worldwide. You will develop easy to use interfaces and connected systems for Extenso project (connected platform to analyze antibiotics in milk).

You will be working in an agile environment, including sprint planning, daily standups and reviewing your peer’s work. You will participate to all the phases of the project lifecycle (form the idea to the product).

Your role will also be to support customers (in French and in English) and correct any problems and questions they may have, with the help of the support team.

2. Profile

  • Do you have a bachelor’s or master’s degree in computer science?
  • Do you have a strong knowledge of C/C++ (Qt)?
  • Can you justify an experience in the development of cloud-based (AWS) web application (Java/JavaScript)?
  • Are you familiar with the Linux operating system?
  • Can you work with Git and continuous deployment systems (Docker, Ansible, Pipelines)?
  • Are you a problem-solver?

 

Beyond this technical knowledge, we are looking for a person who has good communication skills, in French and English and a “Can Do” attitude.

If you are interested, we offer an appropriate compensation package and an exciting and challenging work environment. Considering the fast growth of the company, Unisensor also offers attractive career evolution perspectives, both in terms of role within the company and job content.

Are you interested in this job and think you have the corresponding profile? Do not hesitate to send your CV or video by e-mail to jobs@unisensor.be

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Offres d'emplois

Project manager (Institut National des Radio Éléments)

L’Institut National des Radio Éléments (IRE) recherche un(e)

 

Project manager

Introduction

Pour accompagner sa croissance et renforcer le département « Production Radiochimique », service Downstream, nous sommes activement à la recherche d’un Project manager – Remise en état d’installation de cellules de production radiochimique (H/F).

Fonction

Intégré(e) au service Production radiochimique, vous serez amené(e) à réaliser et à diriger des projets divers de conception, d’amélioration, de rénovation et/ou de remplacement d’installations de production existants sur le site.

Vous participerez également au développement et à l’industrialisation de nouveaux produits tout en assurant le support technique des processus de production et de sureté d’un site nucléaire de classe 1.

Dans le cadre des projets de remise en état d’installation et d’outils de production de radio-isotopes, vous assurerez :

  • La constitution et l’encadrement d’une équipe en charge des actes techniques à réaliser dans les cellules de production à remettre en état ;
  • Le développement d’un pôle de compétences techniques spécialisé dans les maintenances et les remises en état des cellules de production des radio-isotopes ;
  • La gestion d’une petite équipe de collaborateurs :
  • La gestion globale des projets pris en charge et comprenant :
  • La réalisation des cahiers des charges, des plans & schémas de principe ainsi que des estimations financières ;
  • La réalisation des offres et la sélection du matériel, et de sous-traitants pour les activités externalisées ;
  • La gestion des coûts et le suivi des plannings ;
  • Le suivi rigoureux des chantiers et des activités sur le terrain ;
  • La réalisation des retours d’information vers les différentes parties concernées, et les comités de suivi ;
  • La mise en place de méthodologies respectant les exigences de qualité, de sécurité et de sureté.

 

Cette fonction rapporte au Responsable du Service Downstream Production

Profil

  • Ingénieur avec une orientation technique/scientifique (Master 4 ou 5 ans) et présentant les compétences suivantes :
  • Une expérience confirmée en gestion de projets ;
  • Une expérience en maintenance d’installation et d’outils de production ;
  • Des bonnes capacités de communication, de leadership et à travailler en équipe ;
  • Une bonne capacité à guider son équipe et à la faire évoluer ;
  • Des bonnes capacités à travailler de manière indépendante, organisée et méthodique ;
  • Une expérience réussie de minimum 5 ans dans des environnements industriels multiples. Une expérience des milieux pharmaceutique et nucléaire est un atout ;
  • Une approche critique et orientée solution ;
  • Un comportement rigoureux et soucieux des aspects qualité, sécurité et sureté ;
  • Des bonnes capacités de rédaction et de présentation orale ;
  • Une excellente maîtrise des outils informatiques standards (suite office, ERP). La connaissance d’outils informatiques liés à la DAO et la gestion de projet est un atout ;
  • Une bonne connaissance de l’anglais technique.

 

Offre

Un contrat à durée indéterminée ;
L’opportunité d’intégrer une structure industrielle renommée et innovante ;
Un salaire attractif reprenant des avantages extra-légaux, en ligne avec votre expérience.

 

Intéressé(e) ?

Cliquez sur le bouton ‘Postuler’ pour envoyer votre candidature.

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Offres d'emplois

Quality Manager (ABB)

ABB (Charleroi) recherche un(e)

 

Quality Manager

 

Join ABB and work in a team that is dedicated to creating a future where innovative digital technologies allow greater access to cleaner energy.

As a Quality Manager, you drive customer satisfaction and experience by establish and maintaining a passion for quality culture within the organization. As a member of the Quality team, including some global product group responsibility, you are responsible for assuring and controlling quality with systems, processes, and tools to ensure organizational capability and responsiveness to exceed customer expectations while ensuring sustainable operations.

Also, you assume global leadership for audit programs and support the global, regional and local organization to set up quality improvement programs and lean six sigma initiatives.

Sounds like an interesting and challenging role? We are looking forward to your application!

Your Responsibilities

  • Perform own and enable organization to perform audits and ensure the use of analytics of Quality data from all parts of the business to identify risks, failures and non-conformances within the businesses
  • Organizing internal and external audits of the company’s relevant Management Systems to ensure the operation systems.
  • Establish and drive top X customer issue resolution process in collaboration with business line, hubs and local units and ensure cross-organizational support where required
  • Being responsible for improving internal quality processes and procedures to improve overall customer satisfaction, implementing the global and local quality strategy and follow up all the actions locally.
  • Measure and drive KPIs, reduce variation and ensure effective internal controls are in place to meet customer and stakeholder requirements across the whole value chain
  • Develop and implement KPI to measure and drive customer satisfaction in systematic way
  • Being responsible for reporting and review for relevant required Quality Report.
  • Ensuring the use of quality data analysis, use of quality tools, and continuous improvement and providing relevant quality training to local teams.
  • Establish quality improvement programs (QIP) to prevent mistakes and defects in production and products.
  • Establish a structured process of cooperation with the Supplier Quality role in order to define and improve the incoming quality of the worst 5 suppliers.

 

Your background

  • Engineering degree, preferably combined with business knowledge
  • 8-10 years of experience in quality, supply chain or similar functions
  • Knowledge of market/customer’s needs in B2B, preferably with HV components and/or service experience
  • Understand key drivers of customer experience and satisfaction
  • International experience and intercultural sensitivity
  • Fluent communication both in English and French: other languages would be considered a plus
  • Global business understanding
  • Strategic and analytical thinking
  • Problem-solving abilities and quality/OpEx methodologies
  • Networking, leadership, superior communication & negotiation skills
  • Knowledge of Six Sigma approach (Green Belt certification) and continuous improvement approach: Black Belt certification would be considered a plus.

 

More About Us

Bring your very own sense of pride and purpose as you help us drive forward the Fourth Industrial Revolution – creating a sustainable future for our planet, and your career.

Join ABB and harness the power of our diverse global network, as you collaborate with and learn from our world-class teams. Above all, challenge yourself every day. Let’s write the future, together.

 

Pour postuler, c’est ici.

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Offres d'emplois

Global Quality Lead in Medical Devices (UCB)

UCB (Braine-l’Alleud) recherche un(e)

 

Global Quality Lead in Medical Devices

 

At UCB, we put our heart, soul and skills into making a difference for people living with severe
disease. Working together to push the boundaries, we blend the best of our talents to unlock innovation.

Will you join us in our pioneering adventure?

To strengthen our Global Quality Assurance department, based in Braine l’Alleud, Belgium, we are looking to fill the position of: Global Quality Lead in Medical Devices.

As a UCB Global Quality Lead in Medical Devices you like to work in an environment where you can:

  • Drive operational Quality Assurance activities for development and commercial activities related to Medical Devices and Combination products internally and at key vendors.
  • Provide specific internal QA support/consultancy for Medical Devices and Combination Products.
  • Closely work in partnership with QA management at vendors sites and collaboration with UCB Technical Operations and other UCB teams.
  • Ensure compliance to Medical Devices regulations, ISO requirements and GMP/cGMP compliance from a quality, safety and efficacy point of view.
  • Be an actor for change and continuous improvement

 

You will report to the Head of Medical Devices QA.

As a UCB Global Quality Lead in Medical Devices, you will contribute by:

Providing expert advice, support and management for technical operational QA and general QA matters for specific vendors, on behalf of UCB, in design/development and/or testing/manufacturing of medical devices and combination products ensuring application of MDR, ISO and GMP/cGMP requirements.

Specifically focused on the following:

Design and development Quality assurance:

  • Oversee Design & Development activities (D&D), from Inputs definition through Design Transfer (including Validation/Verification activities)
  • Review and approve relevant sections of the device design control documentation and/or Technical Documentation File as required
  • Review and approve protocols and reports for Verification & Validation studies, technology transfers, stability studies, etc…
  • Review and approve UCB documentation. Ensure Design History File (DHF) is in place
  • Support Risk Management Activities related to devices. Ensure risk assessments are performed at appropriate stages of development/commercialization and for decision making on issues arising.
  • Ensure deliverables are issued in accordance with the D&D plan
  • Review and approve submissions and responses

 

Vendor quality management

  • Accommodate design & technology transfer and ensure systems alignment between vendor and UCB
  • Performing focused assessments/audits
  • Preparation and negotiation of Quality Agreements
  • Ensure systems alignment between vendor and UCB
  • Facilitate quality improvement activities at vendors and UCB systems
  • Support risk register for the vendor, and follow up on mitigation activities
  • Monitor and trend vendor performance
  • Authority to accept release or block release of Medical Devices
  • Oversee inspection plans at CMO and UCB

 

Quality processes

  • Facilitate investigations and resolution of issues relating to deviation and change management
  • Review and approve deviations
  • Lead/review critical investigations
  • Track CAPA events and closure
  • Oversee/track change controls

 

Provide expert advice and support on operational and general QA activities for projects part of the devices portfolio (Process improvement, Technology Transfers, New products or life-cycle management…):

  • Act as the Operational QA link between selected external vendors within the Medical Device portfolio
  • Assist with regulatory and customer inspections at Vendors. Specifically focus on: Inspection preparation, Support during inspection, Support post inspection observation closure
  • Work closely with staff in the Corporate QA teams (especially CM&C Clinical Supply QA, Corporate Compliance and
  • Affiliate Quality Services) and key Technical Operations teams/Affiliate teams to ensure that all QA services for selected critical vendors are provided in an effective and efficient way
  • Work in accordance with HSE and Corporate policy requirements and drive personal training and development activities to meet the needs of the business and professional career development
  • Support additional projects as requested
  • Provide on-site presence ‘in plant’ or on site at vendor

 

General GMP:

  • Maintain Quality System elements associated with the ISO, MDR and GMP activities in a compliant manner
    Drive/Support projects related to quality system improvement
  • Maintain key performance indicators (metrics) for key operational development QA activities and services associated with the Medical Devices and Combination Products activities
  • Maintain GMP compliance and inspection/audit readiness at all times. Support Medical Devices QA in the inspection/audit preparation activities, during inspection/audit and for closure of inspection/audit observation with associated CAPA commitments
  • Support Medical Devices and Combination Products related inspections
  • Support Management Review Process
  • Support Design Reviews

 

Interested? For this position you’ll need the following education, experience and skills:

  • Master’s degree with minimum 5 years of experience in the pharmaceutical/biologicals/medical device industry in Quality Management position
  • Operational GMP experience or clinical activities experience would be a distinct advantage.
  • Practical experience in development or QA management of Medical Devices and/or combination products
  • Practical understanding of ISO 13485:2016, MDR, ISO 14971 and 21CFR820 and part 4 requirements.
  • Stakeholders management experience (internal stakeholders, external stakeholders as CMOs, etc.)
  • Should have a US and EU knowledge of pharmaceutical and medical devices regulations together with quality principles and techniques.
  • Fluent in English; French is a nice-to-have
  • Take accountability for decisions and actions taken.
  • Ability to work in a cross functional environment
  • Be proactive, confident and enthusiastic during the interaction with colleagues during team work and take the initiative to promote and share/implement best practices.
  • Must possess good interpersonal, verbal, and written communication skills and be able to confidently present information at interdepartmental and external meetings.
  • Ensure free flow of information throughout the sphere of work.
  • Root cause analysis and risk management/assessment skills will be a distinct advantage.

 

Pour postuler, c’est ici.

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Offres d'emplois

Engineering Manager (Neoceram)

Neoceram (Houdeng-Aimeries) recherche un(e)

 

Engineering Manager

 

We are currently looking for an Engineering Manager who, reporting directly to the General Manager, will coordinate the activity of our Belgian and Italian engineering teams.

The role requires combination of strong technical and interpersonal skills that will allow the person, after an initial period of training, to manage the whole engineering operations of the company, from product design to complete manufacturing.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Direct, review and approve product design and changes;
  • Confer with Management, Product & Application and Manufacturing to discuss quote request, project specs and procedures;
  • Coordinate and technically support the engineering team to accomplish goals and directing the integration with technical activities;
  • Develop and implement policies, standards and procedures for the engineering and technical work.

 

EDUCATION and EXPERIENCE required:

  • Master’s degree in Mechanical Engineering or equivalent with minimum 5 years professional experience in the field (Food, Cosmetic or Pharmaceutical filling&packaging industries would be an advantage);
  • Experience in leading an engineering team and technical project management;
  • Knowledge of CAD systems (ideally PTC Creo);
  • Business fluent in English, plus at least another language with French / Italian preferred.

 

Soft skills required:

  • Great organization and rigor, passionate in Mechanics and ideally in ceramics;
  • Excellent ability to organize information and communicate effectively with people from diverse cultures and backgrounds;
  • Problem solving oriented and attentive to details;
  • Dynamic and proactive, able to work in a team while being very autonomous.

 

What we offer:

An open-ended contract and competitive compensation. Key-role within a winning, young team, offering cutting-edge technical solutions to clients around the world. An exciting function with real opportunities for development within a constantly developing multinational company.

Neoceram is an international and dynamic engineering company operating in the sterile/aseptic filling sector.

As leader in its market the company is mainly focused on the development of ceramic solutions for high precision dosage applications such as the treatment of pharmaceutical, cosmetic and food fluid products. Our activity is strongly customer oriented.

We have an international culture and presence.

 

Pour postuler, c’est ici.

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Offres d'emplois

Technical manager: Power & Analogue Electronics for space applications(m/f)

Scalian (Charleroi) recherche un(e)

Technical manager: Power & Analogue Electronics for space applications(m/f)

 

A propos de nous :

Fournisseur international de solutions et d’expertises, incontournable dans ses spécialités du Digital et de la performance des Opérations.

Le groupe SCALIAN accompagne les acteurs majeurs de l’industrie et du service dans la définition et la mise en œuvre rapide de leurs projets sur deux métiers :

Les Systèmes Numériques :

Systèmes embarqués et critiques, IOT, systèmes d’information et solutions digitales pour l’entreprise

La Performance des Opérations :

Management des projets, de la qualité et de la performance industrielle

 

Function

Within a project / product team, you will be required, in the context of on-board space satellite applications, to ensure the coordination of all technical activities occurring during the entire life cycle of a new equipment.

You will be responsible of the equipment at technical point of view working in close collaboration with the Project Manager, the Quality Assurance Manager and with the support of technical experts.

Main activities

  • Manage all the technical aspects of projects from proposal to the delivery of the product to the client
  • Be the technical interface with the customer
  • Verify the compliance to the electrical specifications
  • Verify electrical schematics and the equipment behavior through Spice simulations
  • Write and/or validate test reports, design justifications and various descriptive documents
  • Define breadboard or prototype tests validation procedures and setup
  • Perform design robustness analyzes (Worst Case analysis, Failure Mode and effect analysis, Part stress analysis,…)
  • Write and/or validate Test specifications
  • Support test technicians
  • Analyse and interpret test results
  • The main activities are to coordinate technical investigations when the test results are not compliant to the requirements and perform analyzes to solve them.
  • Participate to all internal project reviews within the company, and external reviews with the customers
    Estimate the duration and costs of the technical activities and coordinate the technical team

 

Profile

  • Master in Electronics / Electricity Engineering
  • General physical sense and orders of magnitude
  • Good experience in an electronic lab environment
  • Capacity for synthesis, analysis, capitalization
  • Sound judgment, able to take decisions
  • Leadership
  • Client-first approach
  • Able to work independently, self-confidence
  • Federator, energetic and resolute
  • Organized

 

Knowledge of :

o Power converters topologies (buck, boost, flyback, …)

o Analog electronics (opamps, resistors, capacitors, inductors, bipolar transistors, ..)

o Digital electronics (HCMOS family, PWM drivers, …)

o Regulation loops, stability criteria’s

o EMI/EMC aspects

o English (spoken and written)

o Design robustness analyzes (Worst case, Part stress, Failure Mode)

Assets :

o Knowledge of Microcap and Simetrix/Simplis simulators

o French (spoken and written)

o Previous working experience in space or aeronautical industry

· Optional :

o Communication systems (CAN, UART, Ethernet, 1553, …)

 

Vos qualités :

Vous aspirez à vous investir pleinement dans un périmètre porteur afin d’atteindre rapidement un fort degré d’autonomie et de maîtrise fonctionnelle.

Vous possédez le goût des contacts, une réelle aptitude à communiquer, et appréciez de travailler en équipe.

Vous faites preuve d’initiatives et d’esprit de synthèse.
Vous souhaitez évoluer dans un environnement stimulant basé sur un management de proximité au sein d’un Groupe qui s’engage pour ses salariés par la formation et l’évolution professionnelle ? Vous recherchez un projet innovant ? Alors postulez !

Nous offrons 

Nous offrons un package salarial compétitif et des conditions extra-légaux intéressantes (voiture de société..). La fonction est variée et offre des moyens pour le développement personnel.

 

Pour postuler, c’est ici.

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Offres d'emplois

Quality Control Inspector – Manufacturing Equipment

Univercells recherche un(e)

 

Quality Control Inspector – Manufacturing Equipment

 

Based in Nivelles you will join a collaborative team full of passionate change-maker.

As Quality Control Inspector you will be part of the QA department and you will collaborate with the manufacturing equipment and supply chain teams.

Your mission will be to implement, maintain and continuously improve the quality oversight activities for monitoring of incoming materials and final consumables for single-use equipment.

To ensure this you will perform inspections on entry materials (mainly plastic components), document testing and review of assembly records, handle non-conformities and issue certificates.

RESPONSIBILITIES

Quality Management System for incoming and end-inspection of materials

  • You will establish, implement, maintain and continuously improve the specific quality procedures and documentation for performing incoming and end-inspection of materials to set up quality conformity (maintenance of specifications, testing documentation, testing methods, equipment)
  • You will evaluate and improve the current processes.

 

Monitoring of incoming materials & consumables

  • You will perform testing of incoming materials/single-use consumables as per established specifications
  • You will document testing of incoming materials/single-use consumables, including the issuance of certificates as appropriate
  • You will issue and handle non-conformity reports
  • You will perform reporting on testing (KPI, periodic reviews)
  • You will conduct internal and supplier quality audits when required

 

REQUIREMENTS / QUALIFICATIONS

  • Bachelor’s degree in a relevant science field desirable, or high school diploma and equivalent industry work experience
  • Previous Quality Control /Quality Assurance experience is a must
  • You have excellent communication skills and you are stress-resistant
  • Overall: you strive for excellence and focus on high-quality products, you are a driven team player and you feel at ease in the challenging and fast-paced biotech universe!
  • Fluent in French and English

 

OFFER

We offer a long-term contract (CDI), a competitive salary package (health insurance, pension plan, meal vouchers…) and the possibility of evolution in an international, dynamic and fast-growing company.

 

Is this appealing to you? Are you a powerful thinker combined with an efficient doer? Apply now!

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Offres d'emplois

Expert Qualité (IPG)

L’Institut de Pathologie et de Génétique (IPG) recherche un(e)

 

Expert Qualité

 

Votre mission :

Assister le Coordinateur Qualité dans le travail quotidien tout en veillant à faire remonter les informations.

  1. Suivi du maintien concernant le Système de Management de la Qualité, du relevé et du traitement des indicateurs qualité, des plaintes, des non-conformités, des demandes d’amélioration, du retour de satisfaction, des suggestions du personnel, de la gestion documentaire, des dossiers de validation de méthodes/machines/Système d’Information, des enregistrements Qualité et technique y compris la Traçabilité;
  2. Suivi des contrôles de Qualité externe ;
  3. Suivi RH (organigrammes, plan de formation, gestion des compétences (habilitation – qualification),…) ;

 

Suivi de la Gestion du Matériel et de la Métrologie :

  • gestion et traçabilité de tous les matériels et de leur identification ;
  • mise en application des procédures de gestion du matériel ;
  • planification des entretiens du matériel ;
  • supervision de la gestion des pannes dans les services ;
  • supervision de la gestion des étiquettes de conformités ;
  • participation à l’élaboration du budget matériel des différents services.
  • étalonnage / vérification des balances, µpipettes, centrifugeuses, tags de températures ;
  • établissement des rapports et des calculs d’incertitudes au niveau de la cartographie des enceintes thermostatiques ;
  • gestion des sondes de références ;
  • traçabilité et suivi des alertes de température.

 

Organise et réalise le suivi des Audits Internes, participe aux Audits Externes ;

Participe :

  • à la préparation et à la présentation de la Revue de Direction ;
  • aux différentes réunions Qualité ;

 

Aide à :

  • la mise en place et au suivi de la Gestion des Risques ;
  • à l’établissement des Processus ;
  • la sensibilisation de la Qualité auprès des acteurs du terrain via la mise en place de formations, de réunions de travail.

 

Etre l’interface entre le Service Qualité et les autres Services en assurant le suivi, l’accompagnement et aide auprès des acteurs du terrain afin que le Système de Management de la Qualité soit respecté au sein de l’IPG.

Votre profil:

Hard Skills/Experience

  • Baccalauréat dans un domaine scientifique ou équivalent par expérience ;
  • Connaissance des approches Qualité ISO 9001 – ISO 15189 – Métrologiques dans le domaine des Laboratoires avec une expérience de qualiticien de minimum de 2 ans ;
  • Connaissances linguistiques: Français, notion d’anglais ;
  • Connaissance en bureautique (informatique) : Word, Excel, Outlook ;
  • Se former aux nouveaux outils et approches de la Qualité.

 

Soft Skills

 

  • Savoir écouter activement, discerner, convaincre et engager ;
  • Être flexible, ouvert aux changements, s’adapter et faire évoluer son travail, adapter son discours selon la situation et selon les personnes ;
  • Être créatif, proactif, prendre des initiatives, proposer des idées, prendre du temps pour réfléchir à de nouvelles manières de faire ;
  • Être organisé, gérer son temps, son stress, ses priorités.

 

Notre offre :

  • Une rémunération en rapport avec votre expérience ;
  • De nombreux avantages extralégaux (titres-repas de 8 €, assurance de groupe, assurance invalidité, garderie pendant les vacances scolaires, ….) ;
  • Régime de travail de 40 heures/semaine avec RTT.

 

Votre candidature est à adresser aux Ressources Humaines via le site web http://www.ipg.be/offres-emploi/ ou à jobs@ipg.be

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Offres d'emplois

Chef de projet – Industrie du futur (M/F)

L’Agence du Numérique recherche un(e)

 

Chef de projet – Industrie du futur (M/F)

 

Contexte

L’Agence du Numérique (AdN), société anonyme de droit public, est l’acteur public wallon qui soutient le développement du numérique en Wallonie. Elle a pour mission la veille sur les innovations technologiques et les usages du numérique, le conseil auprès du Gouvernement wallon et la coordination des actions opérationnelles liées à la transformation numérique du territoire wallon.

Pour remplir ses missions, l’Agence s’appuie sur la stratégie numérique Digital Wallonia

Mission

Rattaché(e) au pôle Secteur et économie numériques, vous participez avec l’équipe aux missions suivantes :

  • Contribuer au développement du secteur du numérique wallon, principalement au niveau des entreprises offrant des technologies numériques avancées ;
  • Soutenir le redéploiement industriel de la Wallonie ;
  • pour une industrie locale, connectée et résiliente.

 

Rôle

En tant qu’expert sur la thématique « Industrie du futur », votre rôle principal consiste à développer les actions et synergies visant à faire du numérique un moteur de croissance des entreprises et un levier du redéploiement industriel.

Activités

Dans le cadre du projet Industrie du futur, vos principales activités sont :

  • Coordonner le déploiement et la mise en œuvre d’actions avec différents partenaires publics : Cabinets, Administrations, OIP, Communes ;
  • Piloter des partenaires publics : sensibiliser, communiquer, lancer et suivre les appels à projets, animer le réseau, etc.;
  • Assurer la mise en œuvre, le suivi et le reporting au bénéfice de partenaires publics (Cabinets, Administrations, OIP, Communes) et privés (entreprises et start-up) notamment en fournissant des données utiles pour évaluer l’impact des actions ;

 

En collaboration avec les équipes de l’AdN :

  • Assurer une veille technologique et un suivi de la conjoncture économique ;
  • Identifier et promouvoir les tendances technologiques, en lien avec le développement industriel ;
  • Soutenir les orientations stratégiques et politiques via la rédaction d’étude, d’analyse et de synthèse ;
  • Présenter et mettre en valeur les projets et des réalisations : présentation, rédaction d’articles, etc.

 

Profil recherché

Conditions d’accès

  • Titulaire d’un master en sciences économiques, en sciences de gestion ou en sciences politiques ;
  • Expérience professionnelle réussie de minimum 2 ans ;
  • Connaissances et intérêts pour les technologies numériques ;
  • Volonté de servir l’intérêt public et d’être un « Ambassadeur Digital Wallonia ».

 

Sont considérés comme des atouts pour exercer ce rôle

  • Expérience en gestion de projets impliquant partenaires privés et publics ;
  • Implication dans une entreprise privée dans le secteur du numérique ou du secteur manufacturier ;
  • Connaissance de l’environnement économique et institutionnel dans lequel l’Agence évolue ;
  • Connaissance de technologies avancées (IA, IoT, AR/VR, Digital Twin, Blockchain, etc.) : activités de consultance, recherche, missions commerciales, projets d’intégration en entreprise, etc.
  • Connaissance de l’anglais et du néerlandais.

 

Aptitudes et compétences comportementales

  • Orientation Résultats – Proactivité : est moteur en ce qui concerne les activités et projets qu’il gère et/ou auxquels il contribue. Suit l’avancement des activités et la réalisation des résultats attendus ;
  • Ouverture – Adaptation : fait évoluer son rôle, ses activités et ses projets en fonction du contexte, des événements ou encore des besoins. Est flexible dans sa façon d’être, de s’organiser, d’apprendre et d’interagir ;
  • Coopération – Esprit d’équipe : guide ses activités et projets en fonction de l’intérêt collectif. Partage ses avis, idées et informations et travaille de manière collaborative ; communique les résultats de ses activités ;
  • Curiosité intellectuelle – Auto-apprentissage : cherche à acquérir les connaissances nécessaires au développement de ses activités et projets. Adopte une posture exploratoire au bénéficie des missions de l’Agence ;
  • Créativité : propose des moyens nouveaux ou différents de ce qui existe déjà. Pour ce faire, adopte une posture ouverte et développe son esprit critique : analyse et évalue les idées partagées.

 

Conditions de travail

  • Contrat à durée indéterminée à temps plein exercé à Namur ;
  • Déplacements réguliers en région wallonne ;
  • Equipe motivée et dynamique ;
  • Package salarial évolutif en lien avec votre niveau de responsabilité.

 

Vous souhaitez postuler ?

Déposez votre candidature UNIQUEMENT auprès de notre Conseil RH CEPHA/Services, au plus tard le dimanche 7 juin 2020 à minuit.

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Offres d'emplois

Production Manager (ACV – Seneffe)

ACV (Seneffe) recherche un(e)

 

Production Manager

 

ACV fait partie du Groupe Atlantic et est une société familiale d’origine française présente dans 70 pays, employant 8000 personnes pour un chiffre d’affaires de 2 milliards d’euros. Elle est spécialisé dans la conception et la production de chaudières préparateurs d’eau chaude sanitaire et ballons d’eau chaude.

ACV Seneffe en Belgique est le site principal (35,000 m²). Il assure la fabrication des produits en acier inox (préparateurs d’eau chaude et chaudières) et certaines gammes de chaudières à chauffage seul. Le site héberge également les départements Product Engineering, Training et Export.

La société compte également un deuxième site dans le New Jersey aux Etats-Unis (10,000 m²), dédié à la fabrication d’échangeurs spécifiques pour le marché américain ainsi qu’à l’assemblage final des préparateurs d’eau chaude et des chaudières fabriqués en Belgique. Le troisième site de production est situé à Novà Dubnica (Slovaquie) et est entièrement robotisé. ACV y produit des ballons (petite capacité) d’eau chaude sanitaire tank-in-tank en acier inoxydable.

Tous les sites sont certifiés ISO 9001 (2015), notre client investit continuellement afin d’augmenter la productivité des deux sites et d’améliorer sa position concurrentielle dans un marché global.

Vos responsabilités

Rattaché au directeur d’usine, vous aurez pour mission d’assurer le volume de fabrication des produits du site afin de satisfaire la demande des clients.

Tâches générales et managériales:

  • Vous participez à la construction du schéma directeur ;
  • Vous proposez des investissements CAPEX afin de faire progresser la performance et les conditions de travail ;
  • Vous définissez et respectez les budgets sous votre responsabilité
  • Vous êtes l’acteur central dans implémentation de la fabrication des nouveaux produits et mise en place des processus

 

Tâches opérationnelles :

Par rapport aux ressources industrielles

  • Vous définissez et pilotez les besoins en effectifs pour respecter les prévisions de l’état programme et du plan stratégique
  • Vous suivez et améliorez la performance (accident de travail, niveau des qualités des produits fabriqués, respect de la mise en ligne, indice de productivité homme et taux de rendement des machines TRS,…)
  • Vous validez les cadences de production de l’état programme et vous mettez les ressources industrielles pour répondre aux besoins définies dans l’état programme

 

Par rapport aux ressources humaines

  • Vous vous assurez quotidiennement de l’application des principes sécurité.
  • Vous anticipez les ressources (hommes et moyens industriels) nécessaire en s’appuyant sur le plan stratégique ainsi qu’aux contraintes journalières
  • Vous facilitez les échanges et s’assurer de la coordination entre ses équipes et les équipes des autres services de l’usine
  • Vous faites progresser et vous motivez vos équipes (ambiance et conditions de travail)
  • Vous participez aux visites CPPT et réunions CE afin de s’assurer que les conditions de travail soient bonnes et en adéquation avec les exigences et valeurs du groupe

 

Votre profil

  • Formation supérieure d’ingénieur spécialisées dans le domaine d’activité de l’entreprise (électrothermie,électricité, mécanique…) ou/et possédant une expérience significative (min.10 ans) dans une fonction dirigeante en production.
  • Vous avez une passion pour la production, aimez le terrain,l’opérationnel
  • Vous recherchez continuellement des opportunités pour améliorer l’organisation, la performance et les procédures par l’introduction d’idées nouvelles ,
  • Vous générez ou identifiez des idées, approches et perspectives innovantes.
  • Vous êtes excellent communicateur ;sens du contact, capacités relationnelles afin de pouvoir gérer les interactions internes et externes multiples au niveau fournisseurs, partenaires sociaux ou clients
  • Vous êtes structuré, avez l’esprit de synthèse vous agissez avec rigueur, tout en restant flexible et pragmatique
  • Compréhension de l’anglais écrit

 

Notre offre

ACV Burnsen vous offre beaucoup de place pour l’initiative personnelle et la possibilité d’impacter les choses
Un environnement de travail agréable respectant l’équilibre vie privée et vie professionnelle
Un package salarial compétitif

Pour postuler, c’est ici.

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Offres d'emplois

R&D Engineer Industrialisation (McBride)

McBridde (Estaimpuis) recherche un(e)

 

R&D Engineer Industrialisation

 

 

As a R&D Engineer Industrialisation, you will be responsible for the following tasks:

  • Developing new formulations as such that the internal and external customer demands are met.
  • Optimise the development process.
  • Assess the industrial impact of the formulation on different parameters: micro logical, corrosiveness and formulation stability.
  • Delivering the correct level of technical support to the Business Unit clusters and customers in order to develop customer relationships.
  • Be actively involved in providing technical support on supply chain industrialisation project.
  • Maintaining regular contact with suppliers to be informed of new concepts, raw materials, and market tendencies.
  • Managing benchmark activities according to the agreed schedule.
  • Be in very close contact with the factories and different departments to identify opportunities of formulation improvement.
  • Identify across the group within the liquid factory, the differences between the processes and what is feasible.
  • Working with a chemist and developing the skills of the chemist.
  • Suggest ideas to continuously improve process and procedure.

 

PROFILE DESCRIPTION

  • You have a master’s degree in Scientific Subject or Industrial Engineer.
  • You have at least 3 years’ experience in detergent or cosmetic product development and preferably some experience of direct report supervision. Experience as an industrial engineer is a plus.
  • You demonstrate fluent communication skills in French and a particularly good knowledge of English, additional languages are a plus.
  • You are skilled with MS Office, Outlook, Interne t and can also work with SAP.
  • You have supervisory, organisational and project management skills and are good at writing scientific reports.
  • You are able to give clear instructions.
  • You have a strong attitude to quality and are real problem solver and decision maker.
  • You show a positive and confident manner when talking to people.
  • As a R&D Engineer Industrialisation you have a good chemical knowledge and the attitude to enlarge this knowledge within the working domain.

 

OFFER

McBride gives you the chance to work for the European #1 in household products.
Take on a new challenge and an interesting job with the opportunity for self-development.
We offer you varied work in the development lab field but as well on the field.
Finally, we offer the chance to work in a dynamic team where teamwork is essential as well to decorate the Christmas tree.

INTERESSED?

Apply via this link

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Offres d'emplois

Head of Biotech Sciences Smart Labs

UCB (Braine-l’Alleud) recherche un(e)

 

Head of Biotech Sciences Smart Labs

 

 

To strengthen our Biotech Digital Sciences team, based in our hub in Braine, we are looking for a talented individual to fill the position of: Head of Biotech Sciences Smart Labs.

As a Head of Biotech Sciences Smart Labs, you will lead the digital business transformation initiatives of the Biotech Sciences organization aiming at improving the way we capture, exchange and access experimental data, while enabling a proper traceability across development activities (e.g. batch / sample identification & tracking).

You like to work in an environment where you can:

  • Partner with world class scientific teams and together refine and implement the concept of truly smart laboratories seamlessly integrating digitalization, automation and miniaturization.
  • Establish a strong network with the different Biotech Sciences development groups, but also with other UCB laboratories, learning from each other and making sure that our practices are aligned.

 

You will contribute by:

  • Engaging with key stakeholders from the various Biotech Sciences groups (upstream, downstream, formulation, analytical, characterization and clinical manufacturing) across Belgium and the UK to define our common target laboratory system and data architecture.
  • Driving simplified equipment data acquisition and experiment data capture (e.g. barcoding, RFID) initiatives across the Biotech Sciences organization and shaping/refining our future roadmap (e.g. laboratory workflow management, high-throughput system integration).
  • Taking the business ownership of laboratory systems used by the Biotech Sciences organization (incl. ELN, LIMS), making sure they remain up-to-date and evolve in line with our digital transformation needs.
  • Leading and managing the team responsible for designing, delivering and ensuring the consistency of the electronic laboratory notebook (ELN) templates supporting the activities of the Biotech Sciences groups (incl. underlying data catalog).
  • Defining the approach and guideline to meet data integrity requirements in collaboration with key stakeholders (incl. quality assurance, IT, validation and other development groups) and making sure these principles are adhered to.
  • Collaborating with the Biologics Pilot Plant to shape the technology and project roadmap allowing to move towards paperless clinical manufacturing operations.
  • Staying on top of the latest technology trends in your area of responsibility.
  • Working across boundaries, maintaining a proper level alignment with similar UCB departments such as Pharma Sciences (process development for small molecules), but also with partner departments like Early Solutions, Manufacturing & Engineering and Regulatory Affairs.

 

Interested? For this position you’ll need the following education, experience and skills:

  • Master’s degree in Engineering, Information Science, Computer Science or a similar discipline, or alternatively in Biotechnology / Biology with a strong affinity for computerized systems.
  • At least 10 years of experience, amongst which 5 years in the biopharmaceutical industry or related. Experience in the field of process development, discovery or GMP production of biologics is a plus.
  • Experience in leading and managing a multi-disciplinary team.
  • Strong experience in computerized system deployment is a must; knowledge of laboratory & manufacturing applications (ELN, LIMS, MES, …) and scientific data management systems is a significant asset.
  • Strong interest in digitalization, automation and miniaturization, and belief in their potential to transform the way laboratory work is organized.
  • Participation in data integrity related programs and/or in the implementation of GxP relevant systems is an additional asset.
  • Demonstrated ability to analyze stakeholders needs and derive a strategy followed by execution.
  • Demonstrated skills in business process re-engineering and change management.
  • Strong teamwork and communication skills. English is mandatory, French is an asset.

 

Why you should apply

At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.

If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.

Pour postuler, c’est ici.

 

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Offres d'emplois

Compliance Expert (IBA)

IBA (Louvain-la-Neuve) recherche un(e)

 

Compliance Expert

 

 

Job Description

General Mission and Responsibilities :

As an Electrotechnical Compliance Expert in the Systems Engineering department, you will take part in the design and development of world leading products for Intensity Modulated, image guided Proton Therapy and other medical devices or industrial devices with radiopharmaceutical and sterilization applications using ionizing radiations.

These technologies involve complex, large scale, cutting-edge computerized electrotechnical systems

In this role, you will be part of a multidisciplinary teams in every product IBA designs.

  • You will bring your experience and your rigor into compliance of our products to Electrotechnical and Electromagnetic International standards.
  • You will manage Requirements engineering, Risk engineering and Verification activities related to these standards and overall product safety.
  • You determine the strategy to ensure overall compliance of new developments to applicable international ISO / EN / IEC standards.
  • You translate their specific requirements into product specifications and test procedures, and you identify need for required actions for product changes.
  • You share your expertise into large projects of certification and support submission approval of complex medical systems.
  • You support and coach development teams, testing teams and laboratories in the application of these standards and industry best practices during all phases of the product lifecycle, including involvement in design reviews and verification activities.
  • You take part in the IEC CTF Activities, maintaining the tests procedures and managing contacts with external laboratories.

 

Profile You Have

  • You have a master’s degree in engineering (electrical, electro-mechanical, electronics) or a master in fundamental sciences or similar background
  • You have strong knowledge and a proven proficiency of compliance for standards for large scale industrial equipment, preferably in the medical device industry.
  • You have minimum 5 to 10 years’ experience in applying IEC/ISO standards, preferably in the medical device industry and / or in a testing and certification laboratory
  • You have experience in specifying requirements for large scale complex electromechanical systems and submitting devices to certification in a demanding context.
  • You have experience in risk engineering techniques and risk management process.

 

And You Are

  • You have eye for details, and a structured mind. You are able to remain focused and organized in a high level of business expectancy and a demanding context.
  • Autonomous and proactive, you have excellent communication and listening skills, even in exposed situation.
  • Real team player, you share your experience and knowledge, passionate about building bridges with others to reach the goal together.
  • Quality focused, you work with the highest value for your multiple stakeholders, with integrity while ensuring the best pragmatic solutions.
  • Given the international environment, you have full professional proficiency in English (verbal and written). French is an asset.
  • You are willing to travel worldwide (up to 20% of your time)

 

Company

IBA is a cancer diagnostics and treatment company and the worldwide technology leader in the field of proton therapy. The Company’s expertise lies in the development of next generation proton therapy technologies and radiopharmaceuticals that provide oncology care providers with premium quality services and equipment, including IBA’s leading fully integrated IntegraLab® radiopharmacy system, and Dosimetry advanced solutions for Quality Assurance of medical equipment and increased patient safety.

Headquartered in Belgium and employing more than 1,500 people worldwide, IBA currently has installed systems across Europe and the US and is expanding into emerging markets.

The Company is focused on providing solutions in the fight against cancer.

Offer

If you are stimulated by multicultural challenges, we offer you the opportunity to join a team of more than 40 nationalities working on more than 45 different sites on 3 continents.

IBA offers you a competitive performance based compensation package and a flexible work environment. You have real possibilities to evolve within IBA’s worldwide, leading organization and to create your own career path, supported by training programs to acquire new skills and ensure they stay sharp.

As an Equal Opportunity Employer IBA is committed to a diverse workforce.

Pour postuler, c’est ici.

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