Sr. Specialist, Pharmaceutical Analysis
- Responsible for analytical equipment set-up, troubleshooting, and for calibration and preventive maintenance of analytical instruments and software including HPLC, LC/MS, GC, UVVIS, FTIR, Dissolution, Disintegration Apparatus, etc. as per current or future regulatory standards and complete peer
review.
- Research and develop new instrumentation to aid in high efficiency analysis utilizing new technology and automation opportunities in the field.
- Write, review, approve, and execute analytical procedures, transfer/verification/validation protocols and reports for analysis of pharmaceutical raw materials, intermediates, and finished products as per current or future applicable regulatory standards.
- Establish, develop, and/or optimize analytical methodology to test the identity, strength, purity, potency and stability of raw materials, intermediates and finished products according to
official compendial or in-house methods.
- Train and supervise junior staff on instrumentation, operating procedures, test method, protocols and other work matters as necessary.
The position requires Bachelor’s degree in Chemical Engineering, Pharmaceutical Sciences, or Chemical Sciences with 3 years of experience as a Specialist, Pharmaceutical Analysis.
Email resumes to hr@rd2rx.com