Quality Control Chemist
Company Summary: A small privately-owned pharmaceuticals CDMO, specializing in generics, is currently seeking a driven, motivated, and multi-faceted Quality Control Chemist. This role will be located in the greater Atlanta area. The Quality Control Chemist will play a critical role in release and stability testing.
The Chemist will be responsible for:
- Conduct HPLC and other analytical testing on raw materials, intermediates, and finished products.
- Execute method validation and verification studies for HPLC methods in accordance with regulatory requirements.
- Conduct stability studies to evaluate the shelf life and degradation profiles of pharmaceutical products.
- Maintain and calibrate laboratory equipment to ensure accurate and reliable test results.
- Document all test procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Investigate and troubleshoot any deviations or out-of-specification results, implementing corrective and preventive actions as necessary.
- Serve as a mentor for newer teammates.
The Chemist should have the following qualifications:
- Bachelor's degree in Chemistry (or related field)
- Minimum of 2 years of experience in quality control within the generics space
- Proficiency in HPLC analysis
- Strong understanding of regulatory requirements and quality standards applicable to pharmaceutical manufacturing (e.g., FDA regulations, cGMP guidelines).
If you see yourself in this Chemist role and are interested, then please don't wait to apply.
