Job Description
Job Description / Responsibilities
- Perform track and Coordinate stability study samples.
- Evaluate physiochemical test on reference drugs.
- Monitor and supervise production process.
- Monitor and coordinate process validation.
- Evaluate and interpret analytical data.
- Coordinate technology transfer activities.
- Monitor QC/QA analysis of formulation trials.
- Literature review on new products.
- Coordinate Pre formulation and formulation activities of In house new developed products and line extensions.
- Draft batch records, supervise the manufacture of Exhibit batches and assist on the transfer of processes to Production.
- Contribute to timely new product introduction in accordance with cGMP and ISO standards.
- Analytical Method Verification and Validation.
Qualification / Experience
- First Degree (B.Sc / HND / B.Pharm-Science related discipline (Chemistry / Biochemistry).
- 2 - 3 years experience in Pharm manufacturing environment
Skills Required:
- Knowledge of pre-formulation studies
- Understand chemistry of API regulations and guidelines
- Unit process and operations
- Up to date with GMP and regulatory Guidelines and Knowledge of product life cycle