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 play a crucial role in daily manufacturing operations within a cGMP environment, focusing exclusively on upstream processing activities. This role requires hands-on experience with aseptic techniques and a solid understanding of aseptic processes to ensure compliance with regulatory standards and maintain high-quality production.
Key Responsibilities:
- Prepare and operate bioreactors and fermenters using disposable and traditional bioprocess equipment.
- Perform microbial and mammalian cell culture tasks with strict aseptic techniques.
- Prepare stock solutions, buffers, and media, including filtration and sterilization processes.
- Monitor upstream processing operations, identify deviations, and escalate issues as needed.
- Maintain cleanroom standards and adhere to cGMP and SOPs.
- Document batch records and support quality and compliance activities.
- Collaborate with cross-functional teams to ensure smooth production workflow.
Requirements:
- Proven experience in upstream processing within pharmaceutical or biotech manufacturing.
- Strong hands-on aseptic technique skills and in-depth aseptic knowledge.
- 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
Apply online using the form below. Please note that only applications matching the job profile will be considered.