The Quality Assurance (QA) Inspector is a crucial member of the quality unit, responsible for upholding and enforcing all quality and compliance standards across the pharmaceutical manufacturing lifecycle. This role ensures that all materials, processes, and products comply with Current Good Manufacturing Practices (GMP), company policies, and regulatory requirements. The inspector performs a variety of detailed checks, from inspecting raw materials to reviewing final batch records, to ensure the safety, efficacy, and quality of every product released.
Key Responsiblities:
1. Incoming and In-Process Inspection
2. Batch Record Review and Documentation
3. Auditing and Compliance
Qualifications:
1. A Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering, Life Sciences, or a related field is highly preferred.
2. A minimum of 1-3 experience in a Quality Assurance role within a pharmaceutical, biotechnology, or other GMP regulated manufacturing environment.
3. Direct experience with batch record review, deviation investigation, and internal auditing is essential.
4. Thorough knowledge and practical understanding of GMP and FDA regulations.
5. Exceptional attention to detail and a methodical, logical approach to problem-solving.
6. Strong communication skills, both in written and verbal, for effective reporting and collaboration with different departments.
7. Ability to follow company's SOPs and batch records.
Job Type: Full-time
Work Location: In person
