Careers

Working at Univercells

At Univercells, we are on a mission to make health equally accessible to all.
We work every day to reinvent biomanufacturing processes, and develop or integrate the next innovative technologies.
Through the combination of process development and engineering expertise, we create synergies to deliver game-changing production capacities to achieve our mission: Biologics available and affordable to all!

Spontaneous application

Vaccines Process Development Lead

Based in the South of Brussels Region (Belgium), you will join a collaborative team of passionate change-makers.
YOUR MISSION: Provide oversight for upstream and downstream process development activities. In addition, the candidate will drive the development and optimization of an in-house upstream platform process. The position requires in-depth knowledge of mammalian cell culture process development and downstream techniques. The successful candidate shall be an accomplished technical leader with a proven track record, who can operate in a multidisciplinary, collaborative, fast-paced environment.

YOUR RESPONSIBILITIES

  • You will lead the development of a vaccine process development team. Activities include developing, optimizing and transferring the upstream and downstream
  • You will manage a team of Scientists and Technicians (around 10)
  • You will provide technical oversight on all process development related activities including process development, process transfer and GMP manufacturing
  • You will set effective development and manufacturing strategies using current state of the art biomanufacturing technologies and approaches
  • You will be the author and will review protocols, technical reports, batch records, SOPs and CMC sections of regulatory submissions
  • You will conduct root cause investigations and identify solutions to resolve process related issues
  • You will lead cross-functional project teams and you will take a lead role in strategic decisions for development programs;
  • You will manage and guide members of the development team, to ensure delivery of technical objectives, effective collaboration and career development for each group member
  • You will work together with Regulatory, CMCFormulation and Analytical Development areas, including providing data and materials to support efforts in, Formulation and Analytical development

YOUR QUALIFICATIONS AND SKILLS

  • Master or PhD in Chemical Engineering, Biotechnology or other relevant life science disciplines
  • + 8 years’ relevant industry experience, particularly in Vaccine process development
  • Demonstrated technical proficiency, scientific creativity, collaboration with others, and independent thought. Solid knowledge of scientific principles and concepts.
  • Experience participating in and leading cross-functional teams such as CMC teams
  • Proven ability to manage others, assign and schedule work, and conduct performance evaluations.
  • People management experience
  • Ability to work in a fast-paced environment, to multitask and manage multiple projects
  • Ability to independently and rapidly make decisions based on data, scientific knowledge and sound judgment
  • Fluent in English

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.

 

     

    Is this function appealing to you? 

    Apply via LinkedIn and if you have a question drop us an email at job@univercells.com

    Apply here

    Analytical Development Lead - Vaccines

    At Univercells, we are on a mission to make health equally accessible to all. We work every day to reinvent biomanufacturing processes and develop or integrate the next innovative technologies. 

    Through the combination of process development and engineering expertise, we create synergies to deliver game-changing production capacities to achieve our mission: Biologics available and affordable to all!! 

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

    In particular, our Analytical sciences team is a fast growing and energizing group of multinational and high-level professionals. Your role is to lead the Vaccines analytical science team, to support the USP/DSP process development and to supervise the execution of in-process control on Vaccine & Application Projects. 

    Your goal, together with the team, will be also the implementation of analytical laboratory facilities for vaccines development pipeline.

    Responsibilities

    • You will supervise the teamwork and you are able to provide guidance and expertise to advance specific projects and evaluate and propose new technologies and concepts in support of multiple projects;
    • You will plan and conduct scientific/laboratory experiments and evaluate and interpret data and supervise the development and validation of analytical methods (ELISA/ TCID50). You will also design and supervise in process control;
    • You will report results and/or activities and you will write analytical SOP’s and other documentation (protocols, reports, logbooks);
    • You will prepare technical reports and you are able to independently communicate results, presents and defends own work at meetings. You will also deliver updates to senior level management in the context of overall project goals;
    • You will comply with all applicable regulations and will ensure that work performed in the area of responsibility is conducted in a safe and compliant manner. You will also maintain proper records in accordance with SOPs and policies.

    Qualifications                

    • Master or PhD in Biochemistry or Biotechnologies  
    • At least 5 years of experience, Analytical or QC, in vaccine development or vaccines production environment
    • Strong critical thinking, excellent communication and problem-solving skills
    • Ability to design, organize, and coordinate scientific research projects
    • Act as a leader in absence of supervisor and used to provide training and guidance to laboratory personnel
    • Proven knowledge and application of GLPs, ICH, FDA EMA Guidance
    • Experience in technology transfer of analytical methods
    • Able to multitask effectively and independently
    • Innovative and Team player
    • Fluent English

    Technical skills

    • BL3 work (is a MUST)
    • ELISA (D-Ag / HCP)
    • TCID50/CCID50
    • MALS/DLS/NTA, particle characterization
    • Others: CE-SDS/SDS-PAGE/WesternBlot/Total Protein

    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!

    Apply here

    Automation Engineer Software -Nevoline

    Based in Nivelles you will work with a team of design engineers and you will be responsible  for design, specification, programming, simulation and testing of automated controls systems (mostly software) 

      YOUR RESPONSIBILITIES

    • You will ensure that project documentation is in line with the internal procedures and it follows good automation manufacturing practice (ISPE GAMP).
    • You will develop PLC & SCADA application, meeting external and internal customer specifications and functional requirements (software & architecture).
    • You will be responsible for software standard designs and templates able to be reusable on future projects.
    • You will interface with suppliers, projects and product managers and will integrate your planning of development, testing and commissioning of software applications
    • You will prepare specifications for purchase of software licenses and computer devices.
    • You will write functional specifications, performance requirements, users instructions, installation and maintenance manuals & reports.

    YOUR QUALIFICATIONS AND SKILLS

    • Master degree in Automation or industrial engineering
    • 3-5 years’ experience, possibly in process manufacturing (pharma, food, chemical, biotech…) and in a quality-oriented environment
    • Proven experience with PLC (Siemens TIA Portal) and SCADA programming (e.g. Wonderware Archestra…)
    • Good knowledge of Visual Basic .NET (VB.Net) framework and SQL Database
    • Knowledge of industrial electricity and instrumentation is an asset.
    • You are willing to work in a very dynamic and multicultural environment
    • You are a team player and not afraid of challenges
    • You are driven by curiosity and eager to learn every day
    • You have an analytical mindset and you are autonomous, proactive and solution minded
    • Fluent in English. Knowledge of 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.

    Is this function appealing to you? Are you passionate about automation software application? Do you want to work within a great and motivated team? 

    Don't hesitate and apply!

    Apply here

    Scientist DSP - Application Development

    This job is the perfect opportunity to contribute to our mission and be impactful.

    Based in Nivelles, you will join a collaborative team full of passionate change-makers. You will be responsible for the successful development of a smart and continuous innovative downstream process. You will be the one to select and implement the most efficient technologies enabling to simplify and optimize the clarification and capture operations. Working closely with the Upstream Specialist and the Design Engineer, you will also facilitate the integration of the purification process into a completely disruptive continuous production line.

    Responsibilities

    • Lead the design and execution of innovative downstream process programs for vaccine, applications 
    • Screen, select and implement the most efficient single-use technologies that deliver value from R&D to clinics 
    • Integrate innovative clarification and capture operations in a continuous production line chaining upstream and downstream processes
    • Build-up and manage an effective team specializing in purification processes
    • Be responsible for documentation and reach project objectives and deadlines

    Qualifications

    • Master  Degree with a minimum of 5 years of industrial experience in virus purification processes
    • Full understanding of compliance and cGMP considerations 
    • Strong leadership combined with organizational planning and project management skills     
    • Excellent communicator with the ability to transfer knowledge and give confidence to customers
    • Driven by curiosity and eager to learn more every day. With a strong desire to be impactful
    • Fluent English required 
    • Self-motivation and interest for fast-growing companies/SMEs

    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. 

    Is it appealing to you? Are you a powerful thinker combined with an efficient doer? Do you excel in bioproduction and downstream processes?  Apply now 

    Apply here

    Strategy Execution Manager

    Based in Brussels you will be part of the EPMO (Enterprise Portfolio Management Office) and you will support the whole organization for the delivery of various Strategic and/or Corporate projects.

    You will drive a 5Y strategic planning exercise and you will translate it into clear objectives and business actions plan. Your outstanding analytical/strategic-thinking and leadership will support Univercells in his growth and valuable goal creation.

    Moreover, you will lead all aspects of project management from “start to finish” ensuring top quality level of service, deliverables and interactions towards internal and external parties (partners, consortium, clients, …).

    The role is a challenging position that offers broad exposure to strategy development and implementation in a highly entrepreneurial and industrial environment, focused on the latest Life Sciences & Healthcare sector trends driving innovation and disruption in biotechnology, pharmaceutical, medical devices, …

      ?RESPONSIBILITIES

    • Work with business/market owners to identify key business opportunities and issues.
    • Develop analytical frameworks, approach and methodology best practices to analyze strategy opportunities and issues.
    • Design and execute analytics for studying business issues (market research, scenario planning, forecasting, market share, profitability, etc.).
    • Develop technical content (competitive intelligence, market trend analysis).
    • Create documents that inform critical strategic issues and decisions.
    • Apply the right analytical framework, develop solutions and recommendations, represent findings to stakeholders and own the outcome.
    • Support development and present formal recommendations to Univercells’ management.

    QUALIFICATIONS                          

    • Master degree with at least 5 years of experience as management or strategic consultant, in top-tier professional services firms, within Life Sciences, Healthcare & Pharmaceutical Industry.
    • Experience of working with global, multi-cultural, diverse, cross-functional project teams, with demanding timelines and complex deliverables, focused on the research, development, and commercialization of a product, including Regulatory Affairs, Safety, Medical Affairs, Manufacturing and Access.
    • MBA and Project Management Certification or Qualification (PMP, Prince 2, Agile …) are an asset.
    • Demonstrated experience in budget and financial management.
    • Excellent oral, written and verbal communication skills.
    • High level of critical and creative thinking.
    • Flexible, resilient and comfortable with ambiguity.
    • Able to simplify complex ideas for non-experts to comprehend.
    • Possesses high business acumen to build and sustain effective relationships.
    • Providing all support to the team using a servant leadership style whenever possible and leading by example.
    • Fluent English

    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.

    If you are a strategic & entrepreneurial thinker, a team player with a high level of self-motivation and ability to set and meet goals, willing to have an impactful job in a fast-paced and growing company, do not hesitate and apply now!

     

    Apply here

    Logistic Lead

     

    Based in Nivelles you will join a collaborative team full of passionate change-makers. You will lead the development of our new Warehouse Center, supporting our labs & manufacturing activities.

    You will ensure our lab technicians, engineers and production operators have the right equipment and supplies to achieve their mission. The position serves as a liaison for the operations when it relates to supply of consumables, components, semi and finished goods.

    Additionally, you will guarantee the adequate supply of our lab facilities in the Biopark of Charleroi Brussels South.

    You will also oversee outbound shipments, ensuring Sales kit assembly, secondary packaging, transport organization and follow-up.

    This position reports to the Supply Chain Manager. You will be responsible for the efficient operation of the Logistics department across our two sites in Nivelles & Gosselies.

    Your responsibilities

    • You will provide direct leadership and coaching to logistics operators to achieve department objectives and exceed customer and corporate requirements.
    • You will set challenging but realistic SMART goals within areas of accountability. 
    • You will partner with and assist Operations, Quality, Supply Planning & Sales in order to promote a high standard of customer service, proactively identifying and resolving quality and service issues relating to logistics operations. 
    • You will oversee and take part in logistics activities including inventory control, warehousing, transportation, logistics planning, order processing and internal customer service, with focus on best practice and continuous improvement.  You will also support the documentation of logistics processes and work instructions. 
    • You will Supervise WMS (Warehouse Management System) transactions & cycle counts to maintain accurate inventory and reporting systems for finished products, components, packaging and consumables.
    • You will lead logistics projects to drive warehouse efficiency and improvements.
    • You will define, monitor and communicate KPIs & metrics

    Qualifications                

    • Bachelor’s degree or equivalent with 5 years of experience in Logistics or Operations. Pharma or Biotech environment is a plus. 
    • Good working knowledge of warehouse & distribution operations, as well as information systems, transportation and inventory management. 
    • Ability to facilitate projects/focus groups in a team environment while providing team leadership. 
    • Ability to organize change, build relationships, and make good use of available resources.
    • Ability to confront problems and handle conflict.
    • Ability to problem solve and set priorities, generating new ideas and improved ways of working while maintaining effective control.
    • Excellent quality and organization of work (autonomy, methodological approach, behavior under pressure, rigor).
    • Excellent communication (verbal/written) and presentation skills.
    • Working knowledge of Lean Supply Chain (Continuous Improvement Methodology, Kaizen, 5S,…). 
    • Experience with ERP / WMS systems (Odoo is a plus).
    • Working knowledge of Microsoft applications (Word, Excel, and PowerPoint).
    • Enthusiastic and flexible to lead a multitasking role.
    • Strong desire to be impactful.
    • Fluent in English and French

    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!

    Apply here

    QA Specialist - Manufacturing Technologies

    At Univercells, we are on a mission to make health equally accessible to all. We work every day to reinvent biomanufacturing processes and develop or integrate the next innovative technologies. 

    Through the combination of process development and engineering expertise, we create synergies to deliver game-changing production capacities to achieve our mission: Biologics available and affordable to all!

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

    YOUR MISSION:

    You will implement, maintain and continuously improve the quality management system for the development and production of Univercells’ biologicals manufacturing platform. You will report to the Chief Quality Officer.

    RESPONSIBILITIES

    • You will oversee the quality activities for the development and production of the company’s manufacturing platform, regularly monitor the production and machinery to ensure quality on the floor;
    • You will lead, coach and develop your partners in the organisation on the quality requirements for production of equipment for use in the (bio)pharmaceutical industry;
    • You will develop and maintain a comprehensive Quality Management System and tools for the specified operations by setting standards and ensuring continuous improvement of the activities;
    • You will maintain development, product and processes quality by enforcing quality assurance policies and procedures;
    • You will also evaluate and improve the current processes and provide training and knowledge transfer to your business partners;
    • You will ensure appropriateness and compliance to quality standards of supplied goods and manufactured products in line with defined specifications (QA review of incoming material files, batch record review);
    • As a member of the QA team, you will collaborate with your business partners to disseminate quality mindset throughout the operations;
    • As a member of the QA team, you will lead contribute to corporate QA and QMS projects;
    • You will participate in customer audits and ensure appropriate quality actions are being developed;
    • You will perform supplier audits and certifications;
    • You will provide adequate QA/QMS reporting.

    QUALIFICATIONS

    • BSc in Life Sciences or (Bio) Engineering
    • Experience in the development of biomanufacturing technologies is considered an asset
    • Experience in the qualification of pharmaceutical equipment is considered an asset
    • Strong technical understanding of large and complex projects in (bio)pharmaceutical or biomedical device is an asset
    • Understanding of GxP requirements for (bio)pharmaceutical manufacturing
    • Experience with audit and certifications
    • Technical writing skills
    • Strong in communication and team player
    • Good influential and interpersonal skills
    • Ability to work in fast-paced environments and to combine helicopter view and tactical actions
    • Fluent in French and English.

    OFFER
    We offer a long-term contract (CDI or Freelance), 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. 

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

     

    Apply here

    QA Specialist - Quality Systems & Compliance

    At Univercells, we are on a mission to make health equally accessible to all. We work every day to reinvent biomanufacturing processes and develop or integrate the next innovative technologies.

    Through the combination of process development and engineering expertise, we create synergies to deliver game-changing production capacities to achieve our mission: Biologics available and affordable to all!

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

    YOUR MISSION:

    You will implement, maintain and continuously improve the corporate quality management system for Univercells.

    You will report to the Chief Quality Officer.

    RESPONSIBILITIES:

    • You will establish, implement, maintain and continuously improve a quality management system for the corporate activities, including quality manual and quality policies;
    • You will lead and contribute to corporate QA and QMS projects;
    • You will also evaluate and improve the current process and provide training when necessary;
    • You will develop quality tools;
    • You will develop QA/QMS reporting and dashboards and ensure periodic reporting;
    • You will lead the quality management review activities;
    • As a member of the QA team, you will disseminate quality mindset throughout the company;
    • You will participate in health authority inspections and/or customer audits and ensure appropriate quality actions are being developed.

    QUALIFICATIONS:

    • Master’s degree
    • Experience in (bio-)pharmaceutical industry.
    • Experience in setting up and/or contributing to a quality management system is considered an asset
    • Experience with inspections, audits, and certifications
    • Technical writing skills
    • Strong in communication and team player
    • Good influential skills
    • Ability to work in fast-paced environments and to combine helicopter view and tactical actions
    • Fluent in French and English

    OFFER
    We offer a long-term contract (CDI or Freelance), 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.

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

     

    Apply here

    QA Specialist - Development (Bioprocess)

    At Univercells, we are on a mission to make health equally accessible to all. We work every day to reinvent biomanufacturing processes and develop or integrate the next innovative technologies.

    Through the combination of process development and engineering expertise, we create synergies to deliver game-changing production capacities to achieve our mission: Biologics available and affordable to all!

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

    YOUR MISSION:

    You will implement, maintain and continuously improve the quality management system for the pharmaceutical process development of vaccines and biotherapeutics.

    You will report to the Chief Quality Officer.

     

    RESPONSIBILITIES:

    • You will oversee the quality activities for the pharmaceutical development activities in two domains: biotherapeutics and vaccines;
    • You will lead, coach and develop your partners in the organisation on the quality requirements for the development of pharmaceutical products;
    • You will develop and maintain a comprehensive Quality Management System and tools for the specified operations. Setting up the QMS will be the major focus at the beginning of your mission;
    • You will also evaluate and improve the current process and provide training when necessary.
    • You will maintain development, product and processes quality by enforcing quality assurance policies and procedures;
    • As a member of the QA team, you will collaborate with your business partners to disseminate quality mindset throughout the operations;
    • As a member of the QA team, you will contribute to corporate QA and QMS projects;
    • You will participate in health authority inspections and/or customer audits and ensure appropriate quality actions are being developed;
    • You will perform supplier audits and certifications;
    • You will provide adequate QA/QMS reporting.

     

    QUALIFICATIONS:

    • MSc in Life Sciences, Bio-Engineering or related field
    • Experience in development of (bio)pharmaceutical processes is considered an asset
    • Experience in setting up a quality system is considered an asset.
    • Experience with inspections, audits, and certifications
    • Technical writing skills
    • Strong in communication and team player
    • Good influential skills
    • Ability to work in fast-paced environments and to combine helicopter view and tactical actions
    • Fluent in French and English.

    OFFER
    We offer a long-term contract (CDI or Freelance), 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. 

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

     

    Apply here

    EHS Manager

     

    Based In Nivelles you will join a collaborative team of passionate change-makers. 

    ENVIRONMENT: 5 labs (L3 and L2) and an assembling line

    You will give active support for in the implementation of the measures referred to in the Welfare Act. You will also give advice to employer, hierarchical line and workers with respect to Environment, Safety and Health so that a high level of compliance is reached & maintained

    Your goals will be implement maintain and improve environment, health and safety standards, best practices and processes, disseminating EHS topics within the company and ensure that all regulations related to EHS are enforced

     

    RESPONSIBILITIES

    EHS

    • You will participate in the identification of hazards and causes of accident at work and occupational diseases and you will provide advice on risk assessment (chemical and biologic in particular) the overall prevention plan and the annual action plan      
    • You will be the person or reference on the various themes of the code on well-being at work, including working with third parties
    • You will participate to the drafting of instructions concerning: the use of work equipment in lab environment, the use of chemical and carcinogenic substances and preparations, the use of personal and collective protective equipment, fire prevention…
    • You will be the reference in the organization for all matters relating to the application of the legislation
    • You will participate in the application of measures to be taken in the event of serious and immediate danger, in the development of internal emergency procedures and in the organization of first aid
    • You will collaborate in the implementation of preventive measures based on the risk analysis that has been carried out
    •  You will participate in the committee for the reduction of the energy footprint
    • You will ensure coordination with SEPP by providing it with all relevant information to carry out its missions, you will accompany  the SEPP's prevention advisor during workplace visits, and assist in examining the causes of occupational accidents and diseases

    In addition to general missions, as EHS manager you will be in charge of the following tasks :

    • Conduct review of the workplace and workstation, on its own initiative, at the request of the employer, workers or the committee and this at least once a year
    • Examine accidents and incidents and carry out all other investigations deemed relevant to improving workers' well-being, and relative reporting
    • Become familiar with manufacturing processes, work methods, work processes and components of work organization and review them in order to propose measures to reduce risks
    • maintain documentation relating to legislation, hazardous products and preparations and emission points relating to air and water pollution
    • provide the secretariat of the CPPT (where it exists)

    BIOSAFETY

    • You will ensure the communication with the Biosafety Officer and ensure the coordination of the biosafety committee (4 times/year)
    • You will coordinate appropriate training for Lab (training and retraining on biosafety and biosecurity procedure s and practices)
    • You will ensure the archive of the documents in the server and the update of the biosafety manual
    • You will ensure the link with the health provider (Securex)
    • You will ensure appropriate investigations in case of accident and that local rules for the safety of personnel are drawn up and followed

    REQUIREMENTS / QUALIFICATIONS

    • Strong knowledge of EU / Belgian EHSS directives and Regulations
    • Scientific background is a strong asset and prevention advisor level II degree (according to Belgian regulation)
    • Experience in a Lab / pharma / chemical environment is a must
    • Experience in managing EHS compliance in a project environment
    • Risk Assessment and Risk Management knowledge
    • Excellent influencing and negotiating skills
    • Strong team player and customer focus
    • Interpersonal skills to coach and develop employees
    • Strong drive to promote a continuous improvement culture
    • Proven results in matrix environment is an asset
    • Fluent English and French
    Apply here

    Internship

    At Univercells we are always happy to offer internship opportunities to bright and passionate students from bachelor to master degree.

    If you are interested in biotechnologies combined with innovation and meaningful values and mission, do not hesitate to send us your application.

    We welcome students with different background:

    Biotechnology, Biology, Chemistry, Pharmacy

    or

    Engineering (mechanical, electromechanical and automation)

    and also

    Business Administration, Finance, Supply Chain ...

    Do not hesitate and apply now and, please remember to specify in your motivation letter the dates and the duration of the internships.

     

     

    Apply here

    Technical Buyer - Manufacturing

    Based in Nivelles, you will report directly to the Procurement Lead.

    You will join a collaborative team full of passionate change-makers. You will work on the on-time delivery of components and services for Manufacturing and Engineering activities and on stock level management with the aim of ensuring that the concerned teams achieve their mission while complying with the purchasing processes put in place.

    RESPONSIBILITIES

    • You will be responsible for ensuring on-time delivery of components for Manufacturing and Engineering activities (R&D)
    • You will place purchase orders and follow up with the suppliers
    • You will keep track of stock levels and delivery times, following-up on MRP
    • You will manage the database for items/services belonging to your scope, Keeping the ERP system up to date
    • You will perform change of BOMs within the system
    • You will contribute to problem solving and process improvement
    • You will perform reporting for the Procurement Lead
    • Point of contact with the Suppliers for all communication concerning orders
    • Point of contact with Manufacturing and Engineering teams for purchasing purposes
    • Point of contact with Logistic team for purchasing purposes
    • Point of contact with Financial team for invoices issues

    REQUIREMENTS / QUALIFICATIONS

    • First experience in procurement within a (bio)technology environment
    • Experience with ERP / purchasing systems (Open ERP/Odoo is a plus) and good knowledge of Excel
    • Good communicator with the ability to closely manage suppliers
    • Enthusiastic and flexible, able to lead a multitasking role
    • Excellent quality and organization of work (autonomy, methodological approach, behavior under pressure…)
    • Logistics experience is a plus
    • Fluent English and French

    OFFER
    We offer a long-term contract (CDI or Freelance), 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. 

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

    Apply here