Deskripsi Pekerjaan
Join Thermo Fisher Scientific as a QC Chemist I and become a guardian of scientific excellence in our quality control laboratory. This critical role involves performing comprehensive GMP testing across raw materials, in-process samples, and finished products to ensure uncompromising quality standards. You'll leverage advanced analytical techniques while maintaining rigorous compliance with regulatory frameworks, safeguarding data integrity through meticulous documentation and validation processes. Your contributions will directly support our mission to deliver innovative solutions that advance scientific discovery and improve patient outcomes. Collaborate in a dynamic environment where continuous improvement initiatives drive operational excellence and professional growth.
As part of our global scientific community, you'll gain exposure to cutting-edge instrumentation and industry best practices. The 12-hour shift structure offers enhanced work-life balance while maintaining critical laboratory operations. This position is ideal for detail-oriented professionals passionate about upholding quality in pharmaceutical or life sciences manufacturing.
Tanggung Jawab
- Execute GMP testing protocols for raw materials, in-process controls, and finished products using HPLC, GC, and wet chemistry techniques
- Ensure compliance with cGMP, ISO, and regulatory requirements through precise documentation and adherence to SOPs
- Perform equipment calibration, maintenance, and troubleshooting to maintain analytical instrument accuracy
- Investigate OOS results, participate in root cause analysis, and implement corrective actions
- Contribute to continuous improvement initiatives through method optimization and process refinement
- Maintain electronic laboratory notebooks and batch records with complete audit trails
- Collaborate with cross-functional teams to resolve quality discrepancies and support product release
Kualifikasi
- Bachelor's degree in Chemistry, Biology, Pharmacy, or related scientific field
- 1-2 years of GMP laboratory experience in pharmaceutical or biotech manufacturing
- Proficiency in operating analytical instruments (HPLC, GC, UV-Vis, titrators)
- Strong understanding of cGMP principles, regulatory requirements, and quality systems
- Exceptional attention to detail with ability to maintain precise documentation
- Problem-solving skills for deviation investigation and CAPA implementation
- Ability to work independently during 12-hour shifts in a fast-paced environment