
Quality Control Analyst
3 weeks ago
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We are seeking a detail-oriented and analytical Quality Control Analyst to join our R&D team. The ideal candidate must have hands-on experience with HPLC operation, chromatographic data processing, and a solid understanding of various analytical instruments used in pharmaceutical testing. You will play a critical role in supporting product development, ensuring data accuracy, and maintaining regulatory compliance throughout the R&D lifecycle.
Key Responsibilities:
- Perform routine and non-routine HPLC analysis for raw materials, in-process samples, and finished formulations.
- Analyze and interpret chromatographic data using software such as Empower, Chromeleon, or OpenLab.
- Operate and maintain analytical equipment, including UV-Vis, FTIR, dissolution testers, pH meters, Karl Fischer titrator, and balances.
- Prepare and review technical documentation, including SOPs, test protocols, calibration logs, and analytical reports.
- Collaborate with R&D and formulation scientists to support method development, validation, and stability studies.
- Ensure compliance with ICH, GMP, and GLP standards.
- Troubleshoot instrument and method issues as needed.
- Support internal and external audits by maintaining accurate and complete records.
Requirements:
- Master's degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or related field.
- 2+ years of experience in a pharma R&D or QC lab environment, preferably in formulation-based R&D.
- Strong hands-on experience with HPLC operation, calibration, and data analysis.
- Familiarity with other analytical techniques and lab equipment used in pharmaceutical testing.
- Knowledge of regulatory requirements (e.g., GMP, GLP, ICH Q2).
- Excellent documentation skills and attention to detail.
- Ability to work independently and as part of a cross-functional team.
Preferred Qualifications:
- Experience working in formulation development labs or stability testing setups.
- Exposure to regulatory filings (e.g., CTD/ANDA documentation).
- Prior experience with method development and validation.
How to Apply:
Please send your updated resume and a brief cover letter outlining your relevant experience to info@nuvexbiotech.com. Kindly mention "QC Analyst – R&D" in the subject line.
Seniority level- Seniority levelEntry level
- Employment typeFull-time
- Job functionQuality Assurance
- IndustriesPharmaceutical Manufacturing
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