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Associate Scientist

  • Perform physical and chemical testing of raw material, packaging material, in-process, release, and stability samples.
  • Record experimental data, analyze results, and maintain accurate and up-to-date notebooks.
  • Support ANDA/NDA projects form development to approval with guidance.
  • Support method development and method validation work.
  • Assist in maintaining the laboratory in compliance with SOPs, CGMPs, FDA and OSHA.
  • Use and maintain instruments, such as HPLC, GC, Dissolution, UV-VIS, IR, Titrator, etc.
  • Troubleshoot and perform minor maintenance and repair of lab instrumentation.
  • Support investigation and troubleshooting of analytical issues.
  • Carry out duties in compliance with all state and federal regulations and guidelines including FDA, DEA, EPA and OSHA.
  • Assist in writing technical documents (for example specifications, test methods, protocols and reports).
  • Periodically review SOPs for compliance with CGMPs and revise SOPs, if necessary.
  • Perform calibration and maintenance of various analytical equipment.
  • Execute EQ protocols and set up qualification program for new instruments with some guidance.
  • Perform calibration and maintenance of various analytical equipment.
  • Assist in preparing documents for ANDA/NDA filing.
  • Review USP/NF, USP/NF supplements and FPF, as applicable, to make sure company monograph and specifications meet current USP requirements.
  • Assist in reviewing technical documents for content and conformance to USP such as Drug Master File, Technical Packages, Raw Material Specification and Certificate of Analysis.