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

    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

    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

    Senior R&D Design Engineer - Single Use Technologies (SUT)

    Based in Nivelles you will join a collaborative team of passionate change-makers. The Senior R&D Design Engineer will work in the R&D team and will collaborate with the Engineering team in the design and development of innovative bioprocessing products.

    RESPONSIBILITIES

    • You will provide technical guidance and expertise to new product development (NPD) as a lead technical contributor, with responsibility from concept generation to fully commercialized products
    • You will be the team’s recognized technical expert in the areas of:
      • Design and development of single-use bioprocessing consumables, and sensing technologies
      • Thermoplastic welding, sensors, sensing, sterilization, connectivity, filters, filtration, aseptic processing
      • Usage and constraints of Single-Use Technologies (SUT) in pharma environment (integrity test, Gamma irradiation, particles…)
    • You will promote and coordinate project internally within Design, Manufacturing, Documentation and Installation teams
    • You will review customer User Requirements Specifications (URS), prepare deviation list and propose alternative technical solutions
    • You will contribute to realistic project plans, stage gate deliverables, and design reviews. You will also anticipate project roadblocks, delays, and risks and will find solutions without escalation
    • You will interface directly with manufacturing teams to clarify questions on drawings and designs. Assist Manufacturing in troubleshooting production issues on standard and special products
    • You will collaborate with Quality and Product Management to establish appropriate critical to quality (CTQ) metrics

    PROFILE

    • Master on Mechanical or Biomedical Engineering or related field
    • At least 5 years’ experience in Single-Use Technologies (SUT) engineering development
    • Experience with bioprocessing design and development
    • Knowledge and understanding of the current industry guidelines for designing, manufacturing, testing and documenting biopharmaceutical process equipment. (ASME BPE, GAMP, cGMP, ISPE, etc.)
    • Experience in qualification activities (FAT/SAT) for process equipment in the biopharmaceutical industry
    • Able to multitask effectively and independently
    • Project management
    • Innovative and team player
    • Fluent English
    Apply here

    Project Manager (Pharma / Life Science)

    ROLE

    You will support the whole organization on the delivery of various internal and external projects.

    You will be the integrator of product-specific transversal development activities and will deliver one integrated project plan covering all activities. You will focus on tactics and execution.

    You will provide essential support to several projects, working with the Development Lead and other team members to achieve project delivery. You will care about the team functionality and you will increase team efficiency.

    You will act as a champion for Project Management methodologies (Lean), techniques (Prince2), processes (Stages Gates), tools & ways of working, educating colleagues in these areas and sharing best practices across the organization (both for traditional Waterfall projects and for Agile projects).

    The role value for the organization is to engage & align all Univercells people in order that all their efforts & contribution converge towards timely & reliable projects’ delivery.

    RESPONSIBILITIES

    • Framing Project Goals and Objectives in a project charter or similar.             
    • Designing Project Strategies:
      • Use Critical Thinking to design optimal project strategies and scenarios through identifying, developing and employing the right methods and frameworks based on clear goals, benefits and business cases.
      • Inform timely, facilitate quality decision-making and avoid misunderstanding.
      • This includes ongoing strategic alignment, scenario planning as well as ensuring dependencies and interfaces are fully considered.
    • Project Planning, Scheduling, Resourcing:
      • Act as the single point of contact for the overall project budget, planning information, progress tracking and reporting.
      • Partner with Finance to ensure that the team is reviewing the budgets, implementing changes and tracking variances.
      • Manage project activities, budget, resource allocation, critical path, milestones and schedules as required.
      • Closely follow the project schedule, monitoring deadlines for each project task. Check regularly that every deadline is still possible and report any potential delays to the Development Lead.
    • Acting as the guardian of the processes for execution:
      • Deliver projects according to the New Product Development & Introduction Integrated (NPDI2) plan (for vaccines, biotherapeutics and manufacturing technologies). Manage the transitioning to the next stage gate.
      • Deliver projects according to the Product Life-Cycle Change Control (PLC3) process.
    • Organize Project Meetings:
      • Arrange regular meetings with the members of the project: appropriate meeting rooms, materials, calendar invitation, agenda, pre-read information, write & circulate minutes.
    • Maintain Documents:
      • Organize, write and/or track preparation of supporting documents & evidence according to the processes for execution.
      • Maintain and archive crucial project documents which track change progress & approval.
      • File all project documents in an appropriate database or library and ensure that all documents are accurate and have been circulated, reviewed & approved by the Development Lead and Team Members.
    • Risks, Issues and Opportunities Management:
      • Proactively identifies and mitigates issues and risks that could impact the progression of the project while exploring and maximizing opportunities during all stages of the project lifecycle.
    • Measuring Project Performance:
      • Setting and monitoring project quality and performance including KPIs, feedback-based project reviews and identifies opportunities for improvement.
    • Communicating Project Information:
      • Managing the project communication plan to identify the key messages, audiences, interfaces, timings and mechanisms for effective & transparent communication at all levels including externally to the organization.
      • Monitor and summarize project progresses. Prepare reports for upper management regarding the project status.
      • Partners with sponsors, stakeholders and teams to establish a safe, collaborative environment for effective project communications and manages change by motivating towards common goals while championing conflict resolution.
    • Project Management Center of Expertise - Training
      • Drive best in industry practices by contributing lessons learned, challenges, solutions and involvement in process improvement projects.
      • Train colleagues on Project Management Best practices and processes as needed.

    PROFILE

    We are looking for an analytical thinker with solid organizational and problem-solving skills. The successful Project Manager can multi-task in a high volume, fast-paced work environment and is a team player with a high level of self-motivation and ability to set and meet goals.

    In addition, the ideal candidate will also possess the following skills:

    • Master degree and at least 7 years of experience in a Global Project Management Role, or related function, within the Pharmaceutical Industry or its providers.
    • Experience of working with global, multi-cultural and 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.
    • Project Management Certification or Qualification is an asset (PMP, Prince 2, Agile …).
    • Thorough familiarity with word processing, spreadsheet, and project scheduling computer applications.
    • Ability to manage multiple priorities under pressure, troubleshoot, and to meet short- and long-term deadlines.
    • Demonstrated experience in budget and financial management.
    • Excellent written and verbal communication skills.
    • Critical and creative thinking.
    • Ability to build a trusting and safe environment where problems can be raised without fear of blame, retribution, or being judged, with an emphasis on conflicts and problem-solving.
    • Providing all support to the team using a servant leadership style whenever possible and leading by example.

    OFFER
    We offer a long-term contract, 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

    Sales Manager

    Based in our Brussel offices, (but working remotely could be an option) you will join a collaborative team full of passionate change-makers. You will provide direct support to the Head of Sales and will be part of a team of professionals helping us meet our customer's acquisition and revenue growth targets by keeping Univercells competitive and innovative.


    RESPONSIBILITIES 

    • You will be in charge of EMEA Sales and will have an innovative portfolio of products and solutions. 
    • You will cover a whole range of tasks, from prospection of new customers, negotiation  key accounting of existing customers, Prospection and deals closing from initial contact through signed agreements, in a consultative selling process 
    • You will model the financial business cases associated with each sales opportunity 
    • You will structure and negotiate agreements with partners, conduct due diligence, formulate partnership strategies and present recommendations to the management team, as well as manage transactional and execution steps to close.  
    • You will work closely with scientific/technology teams to sell and deploy biotech platforms and services 


    REQUIREMENTS / QUALIFICATIONS 

    • Master degree in Biotech or Engineering field 
    • 5 years of experience working in a sales role (pharmaceutical, medical device, life science/digital health domain) 
    • Solid scientific background, with an in-depth understanding of biopharmaceuticals 
    • Strong network in worldwide or regional life sciences sector 
    • Excellent written and verbal communication skills, ability to deliver key messages to internal and external audiences  
    • Ability to prioritize actions and goals and to successfully progress sales along the sales pipeline 
    • Self-motivation and interest for SMEs 
    • Fluent English, any other language is a plus 


    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

    Analytical Scientist

    Based in our Nivelles labs and offices, you will join a collaborative team full of passionate change-makers. 

    You will be responsible for design, development implementation and execution of analytical methods supporting bioprocess development projects.
    You will supervise and execute the planning/organization of the experiments and developments in your scope of activities.
    You will be responsible for the reporting activities, as protocols and validation results.

    RESPONSIBILITIES

    • Design of innovative analytical methods for vaccines 
    • Develop detailed experimentation protocols and plan.
    • End-to End responsible for the execution of experimentation plans in collaboration with the team of technicians and related data interpretation 
    • Follow-up on deadlines and project objectives within own scope 
    • Troubleshoot experimental works and equipment in support to lab technician 
    • Plan team organization with lab technicians and equipment availability (work planning, supervision of the hands-on plan)
    • Align and follow-up with management and program managers about project status, deadlines, budget, risks…
    • In the matrix organization, upon request of Analytical Lead will participate to Project Management meetings
    • Analyze results and write technical scientific reports 
    • Present results with scientific feedback during internal or external meetings
    • Development, writing and updating of quality documentation, including SOP, work instructions, checklist…
    • Responsible for following procedures according to quality systems within own field of activities Promote and enforce (bio)-safety practices 

    TECHNICAL SKILLS

    • BL3 work (is a MUST)
    • ELISA (Dag / HCP)
    • TCID50
    • MALS/DLS/NTA, particle characterization
    • CE-SDS/SDS-PAGE/WesternBlot
    • Spectrophotometry
    • Liquid Chromatography and DNA by qPCR understanding are an asset

    PROFILE 

    • Master degree or higher
    • Minimum 3 -year experience
    • First experience in analytical methods development (proteins, virus,…)
    • Experience with method transfer is an asset
    • Full understanding of compliance and GMP considerations.
    • Excellent communicator with the ability to transfer knowledge and give confidence to customers. 
    • Driven by curiosity and eager to learn more every day. 
    • Strong desire to be impactful. 
    • Fluent English mandatory
    Apply here

    Technical Writer

    Univercells is looking for a highly motivated and results-driven Technical Writer with excellent communication skills and the proven ability to create great content experiences for customers.


    As a Technical Writer, you will collaborate with a variety of stakeholders and subject matter experts to gather large volumes of complex content, and you translate this into clear and easy to read documents.


    You will work in our Product Management & Marketing team to prepare and maintain documentation pertaining to Univercells’ Manufacturing Technologies including user and internal documentation, technical notes, scientific and generic articles. 


    This position is familiar with biotechnologies concepts and practices.


    Job duties 

    • You write, edit and proofreadManufacturing Technologies documentation, such as User guides, Instruction manuals, Operating manuals, How-to guides, Fact sheets, Frequently Asked Questions (FAQ), Journal and scientific articles, etc.
    • You identify audiences for content and anticipate the questions, problems and needs that the content should convey 
    • You collaborate closely with Engineers and SME’s to obtain an in-depth understanding of the manufacturing technologies we offer, the processes we facilitate and to ensure documentation is comprehensive and accurate
    • You deliver content on time, as stated by release dates and deadlines
    • You ensure the documentation is maintained up-to-date, and drive the review and approval process
    • You deliver high-quality documentation that meets applicable standards 
    • You create from scratch the technical writing internal procedure 
    • You propose and promote writing guidelines and coach colleagues across the organization 


    Qualifications & Skills


    English & Technical writing

    • You have a native (or native-like) English proficiency, written and spoken 
    • You are a talented writer, with the ability to express idiomatically
    • You have a knowledge of the principles and practices involved in technical research, writing, and editing 
    • You have the ability to develop and manage technical documentation according to the company and industry requirements
    • You have a user-oriented mindset and produce documentation that is appropriate for its intended audience, either new or advanced users
    • You have experience in defining a strong, coherent content strategy and delivering high-quality content in line with the business strategy
    • You have demonstrated ability in improving efficiency and quality of documentation processes


    Personal skills 

    • You have the ability to deliver high-quality documentation with attention to detail 
    • You autonomously organize and manage the different steps of the processes
    • You successfully demonstrate a drive for results and excellent time management skills
    • You have excellent communication and listening skills, proactively collecting information from the different stakeholders to efficiently complete the documentation
    • You are comfortable interacting with different departments (mainly engineers, technicians, marketing and business teams) on a daily basis in a dynamic, fast-paced environment
    • You can handle situations presenting conflicting opinions and have a critical mindset


    Technical area & background

    • Bachelor’s Degree in Journalism, English, CommunicationsTechnical Writing, Translation and Interpreting, or other related fields, or equivalent proven working experience 
    • Familiarity with biotechnology, bioprocessing, engineering concepts 
    • Excellent command of Microsoft Office
    • A hand in creating or choosing diagrams, drawings, charts, images, videos, and supporting content to help convey information is an asset


    All candidates will be asked to provide examples or portfolios of their previous works as Technical Writer.

    Apply here

    Marketing Associate

    We are looking for a passionate young talent to reinforce our Marketing & Communication department based in Brussels.

    You will be working in an exciting international and multicultural team of scientists and experts to participate in the implementation of marketing and communication strategies and campaigns, generating leads for commercial success.

    You will be working on all aspects of content and digital marketing, defining and implementing marketing campaigns to support business objectives in term of awareness, activation, sales and retention. 

    This will include content creation and delivery across a variety of online and offline channels:  advertising, congresses, events, direct e-mailings, SEA, social, inbound & content marketing, marketing automation…


    Your main responsibilities:

    • Develop a content strategy and relevant content topics to reach Univercells’ target customers based on marketing & sales objectives
    • Implement a content editorial calendar to manage content and plan specific, timely marketing campaigns on a variety of platforms(paid and organic)
    • Develop content management and leverage the right tools to manage content
    • Content creation and copywriting according to the buying’s journey (articles, infographics, podcasts, webinars, videos, images,etc.)
    • Plan and coordinate Univercells active participation to external events, maximize visibility via workshops and presentations, prepare support material
    • Working in collaboration with internal and external stakeholders for the successful delivery of campaigns across various channels 
    • Report performances and monitor budgets to ensure effectiveness of activity and ROI.


    Requirements

    • Excellent writing and editing skills in English
    • Excellent project management organizational skills, with the ability to prioritize and manage multiple tasks. Strong attention to detail, with analytical and synthetic thinking.
    • Both strategic & hands-on mindset
    • Team-oriented and proactive
    • Being up-to-date about last digital technologies
    • Scientific degree in biology, biotechnology 
    • Or degree in marketing, communication, digital with in-depth knowledge of biotechnology
    • Demonstrate a minimum experience in Digital Marketing, preferably in operational implementation (SEO, SEA, Blog, Content, Social Media, ...)
    Apply here

    Logistic Technician

    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!! 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 ensure our lab technicians, engineers and production operators have the right equipment and supplies to achieve their mission. You will also take part in handling outbound shipments, ensuring Sales kit assembly, secondary packaging and transport organization. Additionally, you will support the preparation of experiments.


    RESPONSIBILITIES

    • Organize and monitor the reception, the storage and the distribution of equipment and supplies to maintain sufficient inventory levels of raw materials and consumables
    • Load and unload shipments using required equipment such as dolly, pallet trucks, forklift, etc
    • Maintain a clean and safe working area by following established housekeeping routines, etc.
    • Execute the cycle and physical counting and manage shelf life of de?ned items.
    • Keep track of quantity, stock levels, delivery times, transport costs and efficiency
    • Arrange warehouse, catalog goods, place products in the stock and process shipments
    • Manage put-a-way of Inventory materials in their assigned bins.
    • Ensure on-time delivery of components for production activities
    • Take care of expedition, contact with forwarder 
    • Receipt and control goods, labeling, sorting, preparation orders, encoding, packaging
    • Perform other related duties as assigned


    QUALIFICATIONS

    • First experience in logistics 
    • Experience with ERP / WMS systems (Odoo is a plus)
    • Working knowledge of Microsoft applications (Word, Excel, and PowerPoint).
    • Good communicator
    • Enthusiastic lead a multitasking role
    • Excellent quality and organization of work (autonomy, methodological approach, behavior under pressure, rigor)
    • Driven by curiosity and eager to learn more every day.
    • Strong desire to be impactful

    OFFER

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

    Apply here