Documentation Officer

Prepare, review, and update documentation such as Standard Operating Procedures (SOPs), batch records, and validation protocols.
Ensure proper documentation of manufacturing processes, quality checks, and equipment maintenance.
Maintain document control systems, including filing, archiving, and retrieval of documents.
Ensure compliance with Good Manufacturing Practices (GMP), regulatory requirements, and internal quality standards.
Coordinate with cross-functional teams to gather necessary documentation and facilitate audits.
Assist in preparing documentation for regulatory submissions and inspections.
Monitor document revision histories and ensure all documents are current and properly authorized.
Train staff on document control procedures and regulatory compliance related to documentation.
Requirements

Minimum of BSc/HND in Science courses with about 3 years cognate experience
Experience in documentation or quality assurance in a pharmaceutical or manufacturing environment.
Knowledge of GMP, regulatory guidelines and validation processes.
Strong attention to detail and organizational skills.
Excellent communication and documentation skill