Overview:
TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.
JOB DESCRIPTION:
Key responsibilities:
- Verification of the companys compliance with ISO/cGMP quality system requirements as well as knowledge of Good Manufacturing Practices.
- Provide immediate support to QA Operations team. Prioritize and manage a variety of projects simultaneously.
- May need to lead and direct the work of others. Organize and Review Master Batch Records (MBR) and supporting documents.
- GMP compliance and Part 11 compliance knowledge preferred. Experience with oversight of documentation systems and the associated aseptic processing regulations.
- Excellent written and oral communication to include accurate and legible documentation skills; ability to work in a fast-paced environment; team oriented; independent work skills and a strong work ethic.
- Microsoft Office and database management skills, organization skills, record keeping skills and ability to handle multiple projects.
- 1-3 Years Experience.
“TekWissen® Group is an equal opportunity employer supporting workforce diversity.”
Job Types: Full-time, Contract
Pay: $40.00 - $43.00 per hour
Application Question(s):
- How many years of experience do you have in documentation systems?
- How many years of experience do you have in aseptic processing regulations?
- Do you have experience with Master Batch Records (MBR) and supporting documents?
Work Location: In person
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