- Support the execution of equipment qualification and decommissioning activities within a GMP-regulated biopharmaceutical manufacturing environment.
- Assist in the preparation, review and execution of qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ), where applicable.
- Perform equipment verification, testing and documentation to ensure compliance with approved procedures and regulatory requirements.
- Support equipment decommissioning activities, including documentation, equipment status verification and closure of relevant records.
- Maintain and update equipment qualification documentation, reports, checklists and validation records.
- Coordinate with cross-functional teams, including Engineering, Manufacturing, Quality Assurance (QA) and Validation, to ensure timely completion of qualification activities.
- Assist in identifying, documenting and following up on deviations or discrepancies identified during qualification activities.
- Ensure all activities are performed in accordance with Good Manufacturing Practices (GMP), site procedures and safety requirements.
- Provide general technical and administrative support for equipment qualification projects
Requirements:
- Min Diploma or Degree in Biomedical / Chemical Engineering / Biotechnology or relevant courses
- No Experience required, training will be provided
- Able to commit for 1 year contract
All qualified and interested candidates please send your resume to *************
Anna Chen jiaxin
CEI No: R25157621
Recruit Express Pte Ltd
EA License: 99C4599