Deskripsi Pekerjaan
Are you a detail-oriented analytical chemist looking to advance your career with a global industry leader? We are currently partnering with a prestigious biopharmaceutical MNC located in the West of Singapore to appoint a Senior QC Chemist. This role is pivotal in ensuring the quality, safety, and efficacy of life-changing pharmaceutical products through rigorous laboratory testing.
In this role, you will work within a high-performance team environment, utilizing state-of-the-art analytical instrumentation to perform complex testing on raw materials, in-process samples, and finished products. The ideal candidate thrives in a fast-paced environment and possesses a strong understanding of cGMP regulations and international quality standards. Whether you are seeking a shift-based role or standard office hours, this position offers unparalleled exposure to international pharmaceutical manufacturing standards and excellent professional development opportunities.
Tanggung Jawab
- Perform routine and non-routine analytical testing using HPLC, GC, UV-Vis, and titration methods.
- Ensure all laboratory activities comply with cGMP guidelines, safety protocols, and internal Standard Operating Procedures (SOPs).
- Conduct data review and documentation for quality control testing to ensure integrity and accuracy.
- Troubleshoot analytical instrument issues and perform basic maintenance to minimize downtime.
- Participate in OOS (Out of Specification) and OOT (Out of Trend) investigations and execute CAPA initiatives.
- Prepare and review laboratory reports, technical documentation, and quality records.
- Collaborate with cross-functional teams, including Production and QA, to address quality-related deviations.
Kualifikasi
- Degree in Chemistry, Chemical Engineering, Pharmacy, or a related scientific discipline.
- Minimum 3-5 years of hands-on experience in a Quality Control laboratory, preferably within a biopharmaceutical or chemical manufacturing environment.
- Strong technical proficiency in chromatography (HPLC/GC) and analytical instrumentation.
- Solid knowledge of USP, EP, and BP pharmacopeia standards.
- Experience in data integrity practices and cGMP documentation.
- Ability to work effectively in a team-based environment and adapt to shift work requirements when necessary.
- Strong analytical, critical thinking, and communication skills.