Qc - Validation Engineer

5 days ago


Singapore ADVANCED MANUFACTURING TECH SOLUTIONS PTE. LTD. Full time

We are looking for a QC Engineer to support **validation of analytical laboratory instruments and computerized systems**in a GMP-regulated environment. The role focuses on ensuring compliance with 21 CFR Part 11, Annex 11, ALCOA+ principles, and data integrity requirements.

**Key Responsibilities**:

- Plan, execute, and document qualification/validation of **analytical instruments**(e.g., HPLC, GC, UV, CDS, LIMS, Empower).
- Prepare, review, and execute **CSV deliverables**such as URS, IQ/OQ/PQ, RTM, and summary reports.
- Perform **data integrity assessments**and ensure compliance with ALCOA+, GDP, and cGMP guidelines.
- Draft, review, and maintain **validation-related SOPs**for QC systems and equipment.
- Support audits and inspections with accurate validation documentation.
- Collaborate with QC, QA, and IT to ensure readiness for **system lifecycle activities**(periodic review, change control, upgrades, cyber-resilience).Contribute to continuous improvement initiatives to strengthen QC lab compliance.

**Requirements**:

- Bachelor’s degree or higher in Chemistry, Life Sciences, Engineering, or related field.
- **5-10 years’ experience**in **CSV/validation of analytical instruments**within QC labs in pharmaceutical/biotech.
- Strong knowledge of **cGMP, GAMP 5, 21 CFR Part 11, Annex 11**, and data integrity frameworks.
- Experience with **microbiology analytical equipment**is an advantage.
- Hands-on use of **Kneat**or other e-validation platforms preferred.
- Strong technical documentation and troubleshooting skills.
- Able to work cross-functionally and support audit readiness.



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