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Laboratory Analyst II
1 week ago
About the Role
Key Responsibilities:- Sample storage and management to ensure compliance with GxP standards.
- Reporting of technical complaints, adverse events, and special case scenarios within 24 hours.
- Distribution of marketing samples as required.
- Performing QC testing on incoming raw materials according to cGMP standards.
- Familiarity with major pharmacopeia standards such as USP, EP, JP/JPE, and ChP.
Deadline Adherence Rate:
- Complete testing on time, reporting missed deadlines promptly.
- Maintain a shortest possible lead time.
- Ensure constant readiness for inspection with no critical complaints/observations.
- Consistently follow GMP and GDP guidelines, SOPs, and implement optimization options to reduce costs.
- Completed training plan.
- Sound technical and scientific knowledge of pharmaceutical and chemical principles.