Job Description:
- We are looking for a Documentation Officer to join our QA team.
- The role involves preparing, issuing, reviewing, and controlling GMP-related documents, ensuring compliance with Good Documentation Practices (GDP), and supporting audits and inspections
Key Responsibilities
- Prepare, issue, and control SOPs, Batch Records, and other QA documents.
- Maintain document master lists, revision control, and secure archiving.
- Ensure compliance with cGMP, GDP, and regulatory requirements.
- Support audits/inspections and coordinate document retrieval.
- Train staff on documentation processes.
Requirements:
- Strong knowledge of GMP/GDP and quality management systems.
- Excellent organizational skills, attention to detail, and proficiency in MS Office.
Qualifications and Skills:
- Industrial Chemistry, Microbiology, Biochemistry, Chemistry, or related field.
- 3 -9 years of experience in QA/Documentation (Pharmaceutical or FMCG).
Salary
Very attractiveApplication Closing Date: Not specified
Application Instructions:
Click the button below to apply
Click here to Apply Join our Whatsapp group
Job Information
Deadline
Not specified
Job Type
Full-time
Industry
Quality control
Work Level
Experienced
State
Nigeria
Country
Nigeria