Asepsis, Biology, Biotech and Pharmaceutical, Cleanroom, Communication Skills, Computer Skills, Current Good Manufacturing Practice (cGMP), Data Entry, Data Quality, Detail Oriented, Environmental Monitoring, GMP (Good Manufacturing Practices), Housekeeping/Cleaning, Laboratory, Lift/Move 40 Pounds, Maintain Compliance, Manufacturing/Industrial Processes, Microbiology, Microsoft Office, Organizational Skills, Presentation/Verbal Skills, Process Manufacturing, Product Development, Quality Control, Team Player, Testing, Water Quality Analysis, Writing Skills
Join Our Team as a QC Environmental Monitoring Associate
Are you ready to take your career to the next level in the thriving biotech hub of Rockville, MD? At Charles River Laboratories, we're seeking a dynamic and motivated individual to join our team as a QC Associate in Environmental Monitoring. This is your chance to be part of a leading CMO industry player, where your skills will contribute to groundbreaking work in microbiological testing and clean room monitoring.
Position Summary
As a QC Associate, you will perform essential microbiological testing and environmental monitoring in classified clean room areas, supporting both planned and in-process manufacturing processes. This role requires a commitment to Charles River's core values of Care, Lead, Own, and Collaborate.
Key Responsibilities
- Conduct viable and non-viable environmental monitoring in both static and dynamic settings.
- Perform water quality analysis, including TOC and conductivity testing.
- Exhibit excellent aseptic techniques and gowning practices for Grade C, B, and A spaces.
- Execute bioburden testing per cGMP guidelines for product development and raw material release.
- Carry out growth promotion, microbial identification, and biological indicator testing in a BSL2 environment.
- Ensure data entry compliance with data integrity expectations and ALCOA principles.
- Support laboratory investigations and handle environmental monitoring excursions and deviations.
- Participate in ongoing lab excellence initiatives as directed by senior staff.
- Flexibility to work outside normal business hours if needed.
Requirements
- Bachelor's degree in Biology or related field.
- Ability to lift up to 40 pounds.
- Capability to work in a clean room suite with appropriate gowning and PPE.
- Excellent verbal and written communication skills.
- Strong organizational skills and attention to detail.
- General computer skills, including Microsoft Office proficiency.
Preferences
- 1-2 years of experience in a GMP facility.
- Understanding of cGMP principles and Data Integrity.
- Experience with aseptic techniques and gowning.
This is an on-site position in Rockville, MD, with no remote work options available. If you're a team player with a passion for science and quality control, we want to hear from you!
Apply now to become a part of our innovative team and make a significant impact in the world of biotechnology!
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