What are the responsibilities and job description for the QC Analyst position at Radiance RPO?
Overview
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
Job Type: Temp-to-hire
Pay: $28.00 - $29.00 per hour
Expected hours: 40 per week
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Work Location: In person
Salary : $28 - $29
