Overview:
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Svaldi.
Job Description:
- Support activities related to documentation review and QC data package generation for product release.
- Reviews data and results of testing completed by QC to ensure compliance to appropriate specifications and protocols.
- Monitoring product and testing schedules and provide notification support to QC. Apply knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices (GLPs) on a daily basis.
- Must have working knowledge of Microsoft Office software and Adobe. Participates in group meetings. Interact with cross-functional group.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
Job Types: Full-time, Contract
Pay: $38.00 - $40.00 per hour
Application Question(s):
- Do you have a Bachelor's Degree?
Experience:
- Quality Control: 1 year (Preferred)
- Good Manufacturing Practices (cGMPs): 1 year (Preferred)
- Good Laboratory Practices (GLPs): 1 year (Preferred)
Work Location: In person
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