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Quality Control Analyst 14172246- 1688584

🔍 Job Opportunity: Quality Control Analyst 🧪👩‍🔬

📍 Location: Winchester, KY 40391

🚫 No C2C Agreements, Locals Only (within 50 miles of Winchester, KY)

⏰ Shift: Monday to Friday, 7:30 AM - 4:00 PM With Ocassional OT

💲 Rate: $24.00 to $29.00 hourly (W-2 contract)

🚧 Onsite Position - Temp to Hire

⏳ Duration: Approximately 6 Months

🔬🧫 Join Our Team in Gene Therapy Environment! 🔬🧫

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.

👩‍🔬 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.

🌟 Key Responsibilities Include: 🌟

  • 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.

🎓 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 (cGMP’s).
  • 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! 🌟💉

Join us in ensuring quality through science! Apply now! 🚀 #QualityControl #Analyticaljob #ScienceJobs

Thank you. We will be in contact soon.

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