Responsibilities:
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.
Valuable 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
Positive in communication