Job Description : Responsibilities :
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 the 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.
Knowledge, Skills, and Abilities :
- 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.
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