Job Description
Sector: Pharmaceutical
Remuneration: 90k to 120k
Responsibilities
- Responsible for document and data control activities
- Performs QA document control function, including login,tracking,processing, approval distributing and archiving in compliance to internal and external requirement.
- Co-ordinates the revision, review and approval by SOPS and GMP documents
- updates and maintenance Quality Assurance operations logs and database
- Responsible for developing and keeping copies of required BMR/BPR for production
- Participate in internal audits and supporting external audits.
- Preparationof quarterly departmental reports for the managing director.
Requirements
- Minimum of BSc/HND in PURE/APPLIED CHEMISTRY, MICROBIOLOGY
- Minimum of 1 to 2 years of experience in a pharmaceutical or manufacturing settings
- Solid knowledge of laboratory analysis
- Excellent Knowledge of Raw materials, laboratory samples.
- A team player.