R&D Analytical Manager

Full Time
Chattanooga, TN
Posted
Job description
ProStaff Workforce Solutions is looking for R&D Analytical Manager to work with a leading chemical company in Chattanooga, TN. Our client is manufacturing a broad variety of products in four primary markets: Active Pharmaceutical Ingredients, Catalysts, Surfactants & Performance Additives for a diverse global market place. If you believe you are qualified, we would be excited to connect and discuss this opportunity in more detail.

Please visit us at https://www.prostaffworkforce.com/ to explore all opportunities.

Direct Hire

Responsibilities:
  • Rugged Analytical method development and Validation.
  • Ensure and monitor laboratory compliance to cGMP.
  • Maintenance and troubleshooting of equipment/ methods related HPLC, LC-MS, GCMS, GC-MS and ICP-MS.
  • Prepare SOPs, guidance, protocols, reports, to support laboratory GMP function in compliance with FDA, ICH and other regulatory guidance.
  • Provide leadership, monitor scientists within group.
  • Communicate with direct report, management, team, internal and external customer about project and business related matter.
  • Stay current with FDA/ICH regulation, analytical literature and analytical technology.
  • Participate in discussion on product strategies.
  • Maintain rigorous accountability and documentation of work related to controlled substance in accordance with established SOP and requirement of federal regulation.
  • Maintain highest standard of scientific professionalism.


Skills & Qualification:
  • PhD in Chemistry with minimum 6 years of experience in Pharmaceutical industry OR M.S. in Chemistry with minimum 10 years of experience in Pharmaceutical industry.
  • Demonstrated knowledge of Analytical development, validation, Analytical instrumentation, Chemistry along with troubleshooting analytical methods.
  • Highest level of skills handling instrumentation such as HPLC/UPLC, LCMS, IC, GC, GCMS including other basic laboratory equipment.
  • Strong familiarization with GLP/ cGMP and FDA/ICH regulation.
  • Knowledge of Organic Chemistry, Inorganic Chemistry and understanding of toxicology is required.
  • Strong ability to communicate analytical results to scientific and non-scientific members.
  • Capable to problem –solve.
  • Meticulous attention to details.
  • Excellent written and oral communication skills.
  • Possess strong time management skills.

Our client offers a competitive compensation package as well as an excellent benefits package for eligible candidates.

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