Manufacturing Associate III (m/f/d)

Manufacturing Associate III

(m/f/d)

Freelance/Contracting project Solothurn Start date: 12/26 Reference number: 901648/1

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Responsibilities

• Execute manufacturing activities according to approved SOPs, batch records, and GMP requirements
• Perform aseptic operations under Biosafety Cabinets (BSCs) and within classified cleanroom environments
• Handle cell culture-based processes and biological materials
• Operate, monitor, clean, and maintain manufacturing equipment
• Verify materials, quantities, and production documentation prior to execution
• Complete batch records and manufacturing documentation accurately and in a timely manner
• Report deviations, discrepancies, and quality events according to established procedures
• Support equipment qualification, validation, and continuous improvement activities
• Ensure compliance with cGMP, EHS, and site safety requirements
• Collaborate effectively with Quality, Engineering, Supply Chain, and other cross-functional teams

Profile

• Solid professional experience in a GMP-regulated pharmaceutical, biotech, or biologics manufacturing environment
• Hands-on experience with aseptic processing
• Experience working under Biosafety Cabinets (BSCs) or Laminar Flow Hoods
• Practical experience handling cell cultures
• Strong knowledge of cGMP and Good Documentation Practices (GDP)
• Experience executing and documenting manufacturing activities within batch records
• Ability to work independently while maintaining high attention to detail
• Strong communication and teamwork skills
• Commitment to quality, compliance, and patient safety

Benefits

• A pleasant work environment
• A varied role at a renowned company
• Support throughout the entire application process