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Quality control manager • austin tx
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Primary role is to perform chemical analysis of pharmaceutical products and routine laboratory operations in a cGMP environment.
Reports to the Quality Control Manager. Internal relationships include Manufacturing, Research & Development, Analytical Development and Quality Assurance.
DUTIES AND RESPONSIBILITIES
Analytical Testing & Review
- Conduct and review routine and non-routine analysis of raw materials, in-process materials, APIs, and finished products in compliance with SOPs, cGMPs, and cGLPs.
- Perform testing using HPLC, GC, GC-MS, ICP-MS, FTIR, UV-Vis, and wet chemistry methods.
- Participate in method validation and method transfer activities.
Equipment & Instrumentation
Documentation & Compliance
Leadership & Team Development
QUALIFICATIONS
WORKING CONDITIONS / PHYSICAL REQIUREMENTS
WORKING HOURS
LOCATION
This position is located in Round Rock, Texas. Rock Round is located 15 miles north of Austin, TX.
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.