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Vaccines Process Development Lead

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The company

Our client is a professional Pharmaceutical and Biotechnology organisation, based in Henegouwen Belgium. Our client is on a mission to make health equally accessible to all. They work every day to reinvent biomanufacturing processes, and develop or integrate the next innovative technologies. Through the combination of process development and engineering expertise, they create synergies to deliver game-changing production capacities to achieve their mission: Biologics available and affordable to all!

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

Role description

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.

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
• 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

Requirements

• 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

Other information

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.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ewout de Jong.

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SIRE Life Sciences®

Listed by: SIRE Life Sciences®
Listed on: 01-04-2019
Country: Belgium
Region: Henegouwen
Employment: Permanent
Expertise: 3 - 5 years
Location Type: On location
Education: Master
Language: English
Sector: Pharmaceutical
Specialisation: Research & Development

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Contact

SIRE Life Sciences B.V.

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 20 658 9800

SIRE Life Sciences Deutschland GmbH

Fünf Höfe
Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

SIRE Life Sciences UK

702 Howard House Dolphin Square
SW1V3PQ London
+44 7307 179882

SIRE Staffing Solutions B.V.

Keizersgracht 440A
1016 GD Amsterdam
+31 (0) 20 658 9804

SIRE Life Sciences Consultancy B.V.

Wetenschapsstraat 14B
1040 Bruxelles
+32 (0) 2 588 1277