Quality Control Chemist Pharmaceutical
7 days ago
- Perform QC testing of raw materials and finished products, including tablets, capsules, and other dosage forms, using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, dissolution apparatus, and particle size analysis.
- Independently interpret and report analytical results while maintaining detailed and accurate laboratory records.
- Ensure compliance with regulatory standards, including FDA and EMA guidelines.
- Operate, calibrate, and maintain analytical instruments and laboratory equipment.
- Collaborate with cross-functional teams, including R&D and production, to support product development and release.
- Provide technical support and training to junior staff as needed.
- 3–7 years of hands-on experience in a pharmaceutical analytical laboratory.
- Proficiency with analytical instruments such as HPLC/UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus.
- Strong documentation skills aligned with cGMP guidelines.
- Ability to troubleshoot analytical techniques and instrumentation.
- Excellent attention to detail and strong problem-solving capabilities.
- Experience working in a CDMO environment.
- Familiarity with ingestible powder and oral solid dosage product testing.
- Knowledge of international regulatory standards and quality systems.
- Bachelor’s degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related scientific field.
- Atrium Care Package available, upon eligibility (including healthcare plans, discount programs, and paid time off).
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