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Microbiology Analyst, Quality Control
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Microbiology Analyst, Quality Control - Contract - Norton, MA
Join our Quality Control team in Massachusetts and turn precision into progress as a Microbiology Analyst.
Proclinical is seeking a Microbiology Analyst, Quality Control to join a team in Massachusetts. This position focuses on maintaining laboratory operations, ensuring data accuracy, and contributing to continuous improvement initiatives.
Primary Responsibilities:
The successful candidate will perform microbiological assays and support quality control activities to ensure compliance with established standards and timelines.
Skills & Requirements:
- Proficiency in microbiological testing techniques such as bioburden, TOC, endotoxin, and conductivity.
- Strong understanding of GMP, GLP, and ICH guidelines.
- Ability to maintain accurate documentation and adhere to testing schedules.
- Experience with laboratory equipment maintenance and inventory management.
- Effective collaboration and communication skills to work with cross-functional teams.
- Commitment to quality, compliance, and continuous improvement.
The Microbiology Analyst's responsibilities will be:
- Conduct routine and non-routine microbiological assays, including bioburden, TOC, endotoxin, and conductivity testing for critical utility samples, in-process samples, and product release.
- Maintain accurate training records and adhere to testing schedules to meet project timelines and quality metrics.
- Assist in the maintenance of laboratory equipment and inventory to ensure smooth operations.
- Submit data promptly and, if qualified, review data to ensure timely availability.
- Perform operational tasks such as critical utility sampling, environmental monitoring, and product testing.
- Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods.
- Adhere to internal policies, SOPs, and regulatory standards (e.g., GMP, GLP, ICH guidelines) to maintain quality and compliance.
- Collaborate with QC and cross-functional teams to support seamless quality control operations.
- Participate in inspection readiness activities and support onsite audits and inspections as needed.
- Support continuous improvement initiatives to enhance QC processes and laboratory efficiency.
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.brigg@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy
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