Job Opportunity: Upstream Processing Specialist (m/w/d)
We are seeking a skilled Upstream Processing Specialist to join our client’s pharmaceutical and biotech production team. The successful candidate will be responsible for performing daily manufacturing operations in a cGMP environment, focusing exclusively on upstream processing activities. This role demands hands-on experience with aseptic techniques and a strong understanding of aseptic processes to ensure compliance with regulatory standards and maintain high-quality production.
Key Responsibilities:
- Prepare and operate bioreactors and fermenters using both disposable and traditional bioprocess equipment.
- Perform microbial and mammalian cell culture tasks while adhering to strict aseptic techniques.
- Prepare stock solutions, buffers, and media, including filtration and sterilization processes.
- Monitor upstream processing operations, identify deviations, and escalate issues as necessary.
- Maintain cleanroom standards, ensuring compliance with cGMP guidelines and SOPs.
- Document batch records and support quality and compliance efforts.
- Collaborate with cross-functional teams to ensure a smooth production workflow.
Requirements:
- Proven experience in upstream processing within the pharmaceutical or biotech manufacturing sectors.
- Strong hands-on aseptic technique skills and comprehensive knowledge of aseptic processes.
- Familiarity with cGMP regulations and cleanroom practices.
- Ability and willingness to work in shifts, including nights and weekends.
- Detail-oriented with excellent documentation and communication skills.
Contract Details:
- Duration: 1 year fixed-term contract
- Shift work required
If you are interested in this opportunity and meet the above criteria, please apply online using the form below. Only applications matching the job profile will be considered.