QC Analyst

ALLTECH CONSULTING SVC INC; Winchester (KY); On-site; USD 45,000 - 65,000; Full time

Job summary

A leading biotech Contract Development and Manufacturing Organization is seeking a Quality Control Technician. This role involves environmental monitoring and microbiological testing to support GMP manufacturing. Candidates should have an Associate's degree in Life Sciences and at least 2 years of relevant experience. Flexibility for off-hours work may be required.

Qualifications

• 2 years of relevant experience in cGMP cleanrooms.
• Experience in cGMP Quality Control.
• Familiarity with Good Manufacturing Practices (cGMP’s).

Responsibilities

• Conduct Environmental Monitoring in cleanrooms (air, surfaces).
• Perform media fills and fill/finish monitoring.
• Communicate results of work effectively through discussions and documentation.

Skills

Attention to Detail

Monitoring Techniques

Microbiological Testing

Education

Associates degree in Life Sciences

Tools

Microsoft Excel

Microsoft Word

LIMS

MODA

Job description

Job Description:

“Paragon Gene Therapy is a growing Biotech Contract Development and Manufacturing Organization (CDMO) with an internationally recognized tradition of quality and service. Paragon Bioservices provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders as well as innovative start-ups utilizing novel technologies to produce state-of-the-art vaccines and therapies for people when they are most in need. As a Paragon employee, you will actively contribute to the delivery of our services and products to our customers and their patients.

This role is responsible for Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II GMP manufacturing. Works in a fast-paced environmental supporting the quality control department of a CMO for manufacturing of biologic bulk drug substance, sterile finished drug product, and fill/finish.

Key Responsibilities include but are not limited to:
• Primary responsibility is in Environmental Monitoring in classified cleanrooms. Monitoring of surfaces, air, and non-viable air quality of ISO 5, 7, and 8 cleanrooms.
• Conducts testing of utilities such as USP water, clean steam, and testing of other manufacturing environments (air, surfaces)
• Builds credibility within the lab group by performing high quality work
• Works closely with manufacturing and QA to coordinate routine EM, changeover EM, and monitoring to support client campaigns
• Performs media fills and fill/finish monitoring which includes continuous monitoring of air quality, personnel aseptic technique, and environment integrity
• Acts as Quality Control authority for aseptic flow and behavior within cleanrooms
• Utilizes MODA to enter, compile, and trend environmental data for reporting purposes
• Works closely with Manufacturing and Quality Assurance staff to resolve quality issues with regard to the facility
• Effectively communicates results of own work through discussions and documentation with some input from supervisor
• Flexibility in following unique campaign requirements that may include off-hour and weekend work
• May conduct bioburden and membrane filtration testing on cleaning, in-process and release samples.

Experience & Education:
• Associates degree in a Life Sciences discipline and 2 years of relevant experience working in cGMP cleanrooms
• Experience working in cGMP Quality Control
• Experience with Microsoft Excel and Microsoft Word
• Strong attention to detail
• Familiarity with Good Manufacturing Practices (cGMP’s)
• Have the knowledge and ability to apply basic scientific and regulatory principles utilized to solve operational, as well as routine quality tasks
• Must be able to work off hours or weekends as required
• LIMS or MODA experience a plus
• Experience conducting bioburden and membrane filtration testing a plus”