- Preparation, review, and control of R&D; documents such as SOPs, specifications, logbooks, and formats.
- Maintain document control systems as per cGMP and regulatory requirements.
- Ensure timely issuance and retrieval of controlled documents.
- Coordinate with various departments for document approval and version control.
- Support internal and external audits related to documentation.
- Good knowledge of cGMP and documentation practices.
- Prepare Process Development Report.
Required Skills
- Must be excellent in written and spoken English; net savvy and adept at computer skills
- Attention for detail
- Team player
- Valuable in communication