Quality Control (QC) Analyst
Position Overview: The QC Analyst is responsible for performing detailed analysis of pharmaceutical products using various analytical techniques. This role ensures compliance with cGMP and company Health & Safety policies while carrying out routine tasks with precision and adherence to strict methodologies.
Key Responsibilities:
- Perform analysis of pharmaceutical products using techniques such as HPLC, UV-Vis, GC, and IR.
- Comply with cGMP standards, executing routine tasks accurately and following strict methodologies for analyses.
- Adhere to the company's Health & Safety policies and procedures.
- Conduct method validations and method transfers as required.
- Maintain and operate standard laboratory equipment, including titrators, pH meters, and more.
Role Requirements: To be successful in this role, candidates should have the following qualifications and experience:
- A relevant degree in a chemistry discipline or equivalent industry experience.
- Proven experience working in a GMP or GLP environment within a pharmaceutical, chemical, or food laboratory.
- Practical knowledge and experience with HPLC and other analytical methods such as GC, IR, and UV-Vis.
Key Words: HPLC, QC, Quality Control, GMP, GLP, Pharmaceuticals, GC, IR, UV-Vis, Method Validation, Health & Safety.