Quality Control Analyst 14172246- 1688584
๐ Job Opportunity: Quality Control Analyst ๐งช๐ฉโ๐ฌ
๐ Location: Winchester, KY 40391
๐ซ No C2C Agreements, Locals Only (within 50 miles of Winchester, KY)
โฐ Shift: Monday to Friday, 7:30 AM - 4:00 PM With Ocassional OT
๐ฒ Rate: $24.00 to $29.00 hourly (W-2 contract)
๐ง Onsite Position - Temp to Hire
โณ Duration: Approximately 6 Months
๐ฌ๐งซ Join Our Team in Gene Therapy Environment! ๐ฌ๐งซ
The facilities of our client are in Gene Therapy environment with a Biotech Contract Development and Manufacturing Organization (CDMO) renowned for its exceptional quality and service. We specialize in providing process development and GMP manufacturing services for Phase I/II clinical trials. Our work supports industry leaders and innovative start-ups in producing cutting-edge vaccines and therapies for those in critical need.
๐ฉโ๐ฌ Your Role:
As a valued member of the ProQuality Network team, you'll play a vital role in ensuring the delivery of top-notch services and products to our customers and their patients.
๐ Key Responsibilities Include: ๐
- Conduct Environmental Monitoring in classified cleanrooms, analyzing surfaces, air, and non-viable air quality.
- Test utilities such as USP water and clean steam, as well as other manufacturing environments.
- Collaborate closely with manufacturing and QA teams to coordinate routine and changeover Environmental Monitoring.
- Perform media fills and fill/finish monitoring, maintaining air quality, personnel aseptic technique, and environment integrity.
- Act as the Quality Control authority for aseptic flow and behavior within cleanrooms.
- Utilize MODA to enter, compile, and trend environmental data for reporting.
- Work collaboratively with Manufacturing and QA staff to address facility-related quality issues.
- Communicate results effectively through discussions and documentation.
- Be flexible to accommodate unique campaign requirements, including off-hour and weekend work.
๐ Experience & Education:
- Associate's degree in a Life Sciences discipline with 2 years of relevant experience in cGMP cleanrooms.
- Experience in cGMP Quality Control.
- Proficiency in Microsoft Excel and Microsoft Word.
- Strong attention to detail and familiarity with Good Manufacturing Practices (cGMPโs).
- Ability to apply basic scientific and regulatory principles to solve operational and quality tasks.
- Willingness to work off hours or weekends as required.
- Experience with LIMS or MODA is advantageous.
- Experience conducting bioburden and membrane filtration testing is a plus.
Join us at ProQuality Network and contribute to groundbreaking advancements in biotechnology! ๐๐
Join us in ensuring quality through science! Apply now! ๐ #QualityControl #Analyticaljob #ScienceJobs