Scientist II; Analytical R&D
CONTRACT PHARMACAL CORP•Town of Smithtown, NY
About The Position
Develop stability-indicating methods. Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis.
Requirements
- Bachelor’s degree in chemistry or analytical chemistry with 4-7 years of pharmaceutical experience OR Master’s degree or Ph.D. in chemistry or analytical chemistry with 1-4 years of pharmaceutical experience
- Instrumentation: HPLC, UPLC, ICP, GC, FT-IR, UV, Dissolution, pH, TOC and Karl Fischer.
- Computer programs: Empower 1-3, EZ Chrome Elite, WindLab, ChemStation, Microsoft Word, Excel and Outlook.
Responsibilities
- Knowledge of USP and FDA requirements.
- Develop stability-indicating methods for Active Pharmaceutical Ingredients (API) and Dietary Supplement products.
- Generate method validation protocols.
- Execute methods validation and methods transfer.
- Generate method validation reports and analytical methods.
- Design and conduct full analysis of Dietary supplements and Active Pharmaceutical Ingredients (API) products and their impurities.
- Conduct assay, content uniformity, dissolution, in-process blend, and blend uniformity of newly developed and stability samples in support of formulation and process development.
- Prepare result documentation for department and general review.
- Identify and resolve problems with analytical methods and provide troubleshooting on instrumentation.
- Conduct Performance Qualification (PQ) on various instruments.
- Provide leadership, guidance and hands-on training to new employee and provide technical support to other departments.
- Effectively communicate information in concise reports.
- Other responsibilities as assigned by Senior Management.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
501-1,000 employees
