Job Description

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

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