Job description
Join a leading multinational pharmaceutical company in the West Region as a Senior / QC Chemist. This contract opportunity offers office hours with optional shift coverage, providing exposure to advanced QC testing in a fast-paced biopharma environment. You will be part of a reputable MNC focused on quality, compliance, and innovative therapies. You will ensure the integrity of analytical data, support release testing, and contribute to continuous improvement initiatives.
As a Senior QC Chemist, you will collaborate with cross-functional teams including QA, Manufacturing, and Validation to ensure GMP standards are met. This role emphasizes method validation, instrument calibration, and robust documentation. You will mentor junior analysts, review data trends, and participate in CAPA investigations as needed. The successful candidate will bring strong technical competence, meticulous attention to detail, and the ability to thrive in a dynamic, regulated environment.
This position offers competitive compensation within SGD 4,500 to SGD 6,500 monthly, with a contract structure suitable for mid- to senior-career professionals seeking stable, long-term project work. If you are ready to contribute to high-quality pharmaceutical products and support a leading MNC, apply today.
Responsibility
- Perform GMP-compliant QC testing on raw materials, in-process samples, and finished products using established analytical methods (HPLC, UV-Vis, GC, titration, etc.).
- Maintain, calibrate, and troubleshoot analytical instruments; ensure method transfer and validation documentation is up to date.
- Assist in method development/optimization and transfer to QC laboratories, under supervision of senior staff.
- Prepare and review data, trends, and deviations, ensuring data integrity and compliant reporting.
- Collaborate with QA, Manufacturing, and Validation to support release decisions and investigation of any non-conformances.
- Lead or participate in CAPA investigations and deviation investigations; drive root-cause analysis and corrective actions.
- Support internal audits and regulatory inspections readiness; ensure adherence to GMP/GLP standards.
Qualification
- Bachelor's or Master's degree in Chemistry, Chemical Engineering, or a related scientific discipline.
- Minimum 5 years of QC experience in the pharmaceutical/biotech industry (senior level preferred).
- Strong working knowledge of GMP/GLP, QA/QC documentation, and data integrity principles.
- Proficiency with analytical techniques (HPLC, GC, UV-Vis, FTIR, etc.) and laboratory instrumentation.
- Experience with method development/validation, stability studies, and software/LIMS/SAP would be an advantage.
- Excellent attention to detail, problem-solving skills, and the ability to work in a cGMP-regulated environment; strong written and verbal communication.
- Ability to work across shifts as required and to mentor junior staff.