Senior Analytical Chemist

Catalent
2dOnsite

About The Position

Senior Analytical Chemist The Senior Analytical Chemist will perform routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. Position Summary This position is 100% on-site at the Greenville site. Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. This role provides laboratory troubleshooting for a team to assist in the successful and timely execution of laboratory analyses.

Requirements

  • Associate degree in Biotechnology, Chemistry or equivalent science degree with seven years of professional experience in pharmaceutical analytical chemistry required or;
  • Bachelor’s degree in a science-related field (e.g. Biology, Chemistry, Pharmaceutical Sciences) with six years of professional experience in pharmaceutical analytical chemistry required or;
  • Master’s degree in a science-related field with five years of professional experience in pharmaceutical analytical chemistry required or;
  • PhD in a science-related field with two years of relevant experience in pharmaceutical analytical chemistry required.
  • Position requires the ability to lift 10-50lbs, unassisted.
  • Majority of the work day is performed while standing, walking, lifting, pulling, and pushing.
  • Requires bending, squatting, crawling, climbing, and reaching.
  • Some exposure to hazardous chemicals and other active chemical ingredients.

Responsibilities

  • Independently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV) of analysis for excipients, new chemical entities and/or drug products.
  • Interpret data and make recommendations to management for improvement or potential concerns.
  • Compare laboratory data against specifications, prepare reports, and trend data where applicable to determine if results meet requirements.
  • Ensure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentation.
  • Ensure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigations.
  • Independently author standard operating procedures, analytical testing procedures, final submission ready documents, and create document templates for use by junior team members.
  • All other duties as assigned.

Benefits

  • Competitive medical benefits and 401K
  • 152 hours of PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes
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