Quality Assurance Professional
3 days ago
We are seeking a highly skilled professional to review and approve engineering documents, participate in alignment meetings with business functions, and support quality systems and GMP standards. The ideal candidate will have a degree in pharmaceutical sciences, life sciences, biology, biotechnology, chemistry, chemical engineering, or a related discipline, and at least 2 years of experience in quality assurance, GMP/GLP compliance, operations, or validation.
Key Responsibilities
- Review and approve engineering documents to meet site goals.
- Participate in alignment meetings with business functions to ensure smooth operations.
- Support business functions in following quality systems and GMP standards.
Requirements
- Minimum degree in pharmaceutical sciences, life sciences, biology, biotechnology, chemistry, chemical engineering, or related discipline.
- At least 2 years of experience in quality assurance, GMP/GLP compliance, operations, or validation.
- Understanding of FDA/EU and ICH guidelines.
- Experience in international regulatory network/audits is an advantage.
Working Conditions
- 5-day work week: 8am - 4.30pm.
- Durations: 6 months (extendible).
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