Direct message the job poster from BioTalent
Recruitment Consultant - Account Management US Contract
We are seeking a highly skilled Senior QC Analyst to join our client's Quality Control team on a 12 month contractual basis (high likelihood of extension or permanent offer), specializing in raw material testing and spectrometry. The successful candidate will be responsible for performing analytical testing on raw materials using spectroscopic techniques such as FTIR, UV-Vis, and ICP-MS/AES, ensuring compliance with regulatory standards (e.g., USP, EP, GMP).
Key Responsibilities:
1. Conduct qualitative and quantitative analysis of raw materials using spectroscopic and chromatographic techniques.
2. Perform method development, validation, and troubleshooting for spectrometry-based assays.
3. Review and interpret analytical data, ensuring accuracy and compliance with cGMP, FDA, and ICH guidelines.
4. Investigate OOS (Out of Specification) and OOT (Out of Trend) results, implementing corrective actions.
5. Collaborate with cross-functional teams to support supplier qualification and raw material release.
6. Maintain and calibrate analytical instruments to ensure optimal performance.
7. Document results in LIMS, laboratory notebooks, and regulatory reports.
Requirements:
1. Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field.
2. 5+ years of QC experience in a pharmaceutical, biotech, or chemical manufacturing environment.
3. Proficiency in FTIR, UV-Vis, ICP-MS, and other spectroscopic techniques.
4. Strong knowledge of GMP, USP, EP, and regulatory compliance.
5. Experience with LIMS and electronic data management systems.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Science, Manufacturing, and Accounting/Auditing
Industries
Pharmaceutical Manufacturing, Research Services, and Biotechnology Research
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