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Job Description
Senior QA Associate
Lead quality initiatives, ensuring compliance with site safety policies and procedures. Monitor quality systems, production areas, and product quality to ensure control.
**Key Responsibilities:**
- Review and approve GMP documents, including SOPs, raw material specifications, and validation documents.
- Re-identify, re-evaluate, and dispose of raw materials and packaging components.
- Evaluate regulatory information and monitor GMP compliance, data integrity, and systems.
**Requirements:**
- 2+ years of relevant experience in a quality-related field.
- Hons BSc, MSc, or PhD in Pharmacy, Chemistry, Engineering, Quality, or a related discipline.
**Attributes:**
- Excellent attention to detail.
- Strong organizational skills and ability to work under pressure.
- Strong analytical and problem-solving skills, with experience in root cause analysis.