Head, Quality Control at Biomedical Ltd

 The Role

• To ensure that the manufacturing production lines run smoothly and generate a consistently suitable output of products that meet quality.
• To coordinates employee and communicate between the Production teams, Quality Assurance Manager and the E.D Technical.
• Devising ways to improve the manufacturing process, reviewing new specifications and procedures for products or processes, and training staff to use them.
• To set the standard requirements for raw materials from suppliers and monitoring their compliance.
• To ensure cGMP rules/ obligations are adequately followed.
• To ensure the laboratory and production equipment are calibrated as at when due.
• Signs all Standard Operating Procedures and other QA/QC documents.
• Ensures Stability Testing of Finished Products.
• Checks for updates in Pharmacopoeias and approves final specifications.
• Serves as a member of Research and Development Committee and conducts tests on new formulations to evaluate the quality of products.
• To oversee the Chemical/Microbiological analysis of the company’s raw materials, packaging materials, In-process and finished products are conducted with approved.
• Keeping accurate documentation and performing statistical analysis which involves collecting and scrutinizing every data /test results.
• Assisting in self-inspection of the factory
• Operational knowledge of analytical instrumentation like HPLC, UV-VIS equipment, Flame photometer etc.
• Proficiency in computer.

Requirements.

• Must possess a minimum of B.Sc / HND in Chemistry, Biochemistry or Industrial chemistry.
• Must have a minimum of Five years post NYSC experience in the pharmaceutical Industry.