job description
Are you an experienced chemist looking to elevate your career in the thriving biopharmaceutical sector? We are urgently seeking a dedicated and analytical Senior / Quality Control (QC) Chemist to join a world-class, global Biopharmaceutical Multi-National Corporation (MNC) located in the West of Singapore.
This is a fantastic opportunity to work in a state-of-the-art laboratory environment, utilizing cutting-edge technology to ensure the safety, efficacy, and high quality of life-saving medical products. We offer both office hours and shift-work arrangements to suit your lifestyle. If you possess a keen eye for detail, strong technical expertise, and thrive in a fast-paced environment, this is the perfect career move for you.
As a key member of the QC team, you will perform analytical testing of raw materials, in-process samples, and finished drug products. You will be instrumental in upholding stringent international regulatory standards and GMP guidelines, driving continuous improvement in laboratory operations.
Responsibility
- Perform routine and non-routine QC testing of raw materials, in-process, and finished products in compliance with GMP guidelines.
- Operate, troubleshoot, and maintain advanced analytical instruments such as HPLC, GC, UV-Vis, and FTIR.
- Execute method validation, verification, and transfer protocols for biopharmaceutical assays.
- Investigate out-of-specification (OOS) and out-of-trend (OOT) results, implementing effective corrective and preventive actions (CAPA).
- Maintain meticulous and accurate documentation of all laboratory activities in alignment with ALCOA+ data integrity principles.
- Assist in internal and external regulatory audits (e.g., FDA, HSA) by ensuring laboratory readiness.
- Participate in continuous improvement initiatives (5S, Lean) to optimize lab workflows and efficiency.
Qualifications
- Bachelor’s Degree in Chemistry, Biochemistry, Pharmaceutical Science, or a related scientific discipline.
- Minimum of 2-5 years of hands-on Quality Control laboratory experience within a GMP-regulated biopharmaceutical or pharmaceutical manufacturing environment.
- Strong technical proficiency in analytical techniques, particularly HPLC, GC, and wet chemistry.
- Familiarity with laboratory software systems (e.g., Empower, LIMS).
- Ability to work independently as well as collaboratively in a fast-paced, dynamic team environment.
- Excellent analytical, troubleshooting, and communication skills.
- Flexibility to support shift work or office hours based on operational requirements.