POSITION SUMMARY :
Looking for candidates at Chemist I, II and III levels responsible for carrying out analytical method validation / verification activities and testing for Oral Solids, Oral Liquids, Topicals and Powders.
MAJOR DUTIES / RESPONSIBILITIES :
- Develop / Validate / Verify analytical (HPLC, GC, ICP-MS / OES, other) methods for assay and impurities determination in drug substances and drug products.
- Perform wet chemistry and chromatographic testing for raw materials and products under development phase
- Perform stability studies for drug products in development phase and generate reports
- Develop and validate cleaning methods and generated study protocols and reports
- Prepare relevant protocols, reports, and final methods
- Maintain proper instrument calibration status
- Ensure that work is carried out safely and in compliance with the organization’s quality system
- Ensure that quality documentation is generated and updated to reflect current best practice in a timely manner.
- Perform peer review at Chemist III level, not required if you’re applying for Chemist I / II levels.
- Perform other duties as assigned.
MINIMUM / PREFERRED REQUIREMENTS :
Education :
Bachelor or Master’s degree in science or Pharmaceutics.
Experience :
Bachelor’s with 2-7 years of experience in a generic pharmaceutical analytical lab. Master’s is preferred. Candidates shall be considered for different positions based on educational qualification and experience. Good understanding of cGMPs is a must for experienced candidates.
PHYSICAL DEMANDS / ENVIRONMENTAL CONDITIONS :
Laboratory and office environmentAble to lift about 25 pounds.Able to stand and or sit for longer period of time.On-site, Full-time, Day Shift