Scientist - Microbiology
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Scientist - Microbiology (PostDoc) voor J&J MSAT Emerging Technology, hybride Schaffhausen, 40u/week, 12 maanden.
- Locatie
- Schaffhausen, CH
- Werkvorm
- hybride
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Gepubliceerd
- Opdrachtgever
- Johnson & Johnson
Eisen
- Pharma background
- English essential
- Experience in analytical development and (continuous) manufacturing process development
- Doctorate in Microbiology or Biopharmaceutical Engineering
- Excellent communication skills, both oral and written
- Knowledge and experience in data analyses and report writing
- Experience in microbiological techniques
- Team player: working in cross-functional teams
Wensen
- Experience with GMP processes
- Experience with large molecule drug substance & drug product manufacturing processes
- PhD in Microbiology, Biopharmaceutical Engineering or equivalent
Omschrijving
Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson. The role is a Scientist - Microbiology position located in Schaffhausen, with a duration of 12 months, 40 hours hybrid. English is essential, pharma background required. MSAT Emerging Technology is recruiting for a PostDoc, located in Schaffhausen. Manufacturing Science & Technology (MSAT) Emerging Technologies plays a key role in driving technology innovation for the J&J Innovative Medicine Supply Chain. Emerging Technologies is responsible for the definition of new opportunities, breakthrough-technologies scouting, lab-scale proof-of-principle studies, and demonstrating proof-of-concept at large scale. The team develops and delivers projects primarily related to two key MSAT strategic pillars: Process Intensification and Integrated Quality and Real-Time Release. The role supports advanced technology projects for process intensification of biopharmaceutical manufacturing through preparation, design, and execution of proof-of-principle and proof-of-concept studies together with scientists and partners in R&D and Supply Chain. Key responsibilities include development of a microbiological control strategy for a continuous Drug Product manufacturing process, coordination of a global cross functional project team for the concept development for non-destructive bioburden testing, PoP (lab-scale) and PoC (at-scale) study design, execution, and reporting, providing input to the technology innovation strategy and business case development, collaborating with business units on next-gen microbial testing, technology scouting and co-development with external vendors, and supporting the Large Molecule Innovation Community. Education: PhD in Microbiology, Biopharmaceutical Engineering or equivalent - preferred. Experience and skills: Doctorate in Microbiology or Biopharmaceutical Engineering, experience in microbiological techniques is a must, experience in analytical development and (continuous) manufacturing process development, knowledge and experience in data analyses and report writing, excellent communication skills, team player in cross-functional teams, experience with GMP processes is preferred, experience with large molecule drug substance & drug product manufacturing processes is a plus. Key competencies: excellent problem-solving abilities, excellent interpersonal and communication skills, technological and digital curiosity, results and performance driven.
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