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QC Associate || Pharma Industry
3 months ago
The primary focus of the Quality Control Associate I role will be to support drug product lot release
and in-process testing within a cGMP environment.
Top Skills:
• BS in Scientific Discipline, preferably Microbiology
• Computer proficiency
• Regulated industry experience
• Strong communication skills
• Demonstrated success working in a high performing, results driven environment
RESPONSIBILITIES:
• Perform or support cGMP lot release, in-process, and stability testing using various software
packages.
• Ensure timely completion of testing and tasks as assigned.
• Support assay transfer and method validation of by executing cross-site validation protocols and
providing data to support final reports.
• Identify opportunities for continuous improvements.
• Maintain instrumentation and equipment preventative maintenance and supporting
documentation in a cGMP compliant manner.
• Assist in the implementation of new assay methodologies and the associated instrumentation.
• Identify and support initiation of Deviations, CAPAs and Laboratory Investigations.
