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 environment
- Able to lift about 25 pounds.
- Able to stand and or sit for longer period of time.
On-site, Full-time, Day Shift