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The Quality Chemist Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures.

 

Primary Responsibilities

  • Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory.
  • Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures.
  • Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.
  • Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting.
  • Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency.
  • Aid other group members as required.
  • Ensure that equipment and working areas are maintained with good safety and housekeeping practices.
  • Re-stock chemicals and consumables used in analysis.
  • Performs other related assignments and duties as required and assigned.

 

Education and Experience Requirements

  • The incumbent must have a BA or BS degree in Chemistry or closely related science. Minimum of 1-year relevant experience preferred.

Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE).

Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position.

 

 

Sponsorships are not available

Future sponsorships are not available

We are not seeking an IT Tester for this role, this role test pharma product.

Last updated on Oct 5, 2023

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