
Manufacturing Specialist
10 hours ago
As a key member of our team, you will play a vital role in the manufacture of Advanced Therapy Medicinal Products (ATMP).
Main Responsibilities:- Perform manufacturing and quality control activities according to Good Manufacturing Practice (GMP) guidelines to ensure the production of high-quality ATMP.
- Identify, report, and support health and safety issues and investigations, as well as identify potential health and safety improvements.
- Maintain work areas in an inspection-ready state at all times.
- Drive personal development and seek opportunities to grow and expand additional capabilities.
- Communicate professionally with team members and other stakeholders.
- Collaborate and deliver continuous improvements within the manufacturing area to enhance safety, quality, and flow.
- Evaluate and resolve quality issues and investigations.
- Ensure individual and co-worker work complies with GMP, Data Integrity, and Good Documentation Practice (GDP).
- Complete necessary training in a timely and GMP-compliant manner before task execution.
- Closure of assigned GMP documentation in a timely manner, first-time correct, and in accordance with procedures.
- Sanitize and monitor facility and materials adequately to prevent contamination or cross-contamination.
- Movement and preparation of materials required for bioprocessing and support activities, including management within the Enterprise Resource Planning system.
- Verify materials used in manufacturing are correct, clean, suitable, and readily available for production in accordance with agreed-upon schedules.
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