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Sr. Environmental Monitoring Technician
Avid BioservicesUnited Statesfull_timeVerifiedPosted 22 Jan 2026
💰 $68,000/yr($50,000/yr – $68,000/yr)
About the role
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: The Sr. Environmental Monitoring Technician performs environmental monitoring and routine microbiological testing within a GMP biopharmaceutical manufacturing organization.
- Perform environmental monitoring such as non-viable particulates, air viables, surface, temperatures in cleanroom environments within the Manufacturing area per SOP.
- Perform environmental monitoring for aseptic filling processes according to SOP.
- Operate monitoring equipment that includes but is not limited to Laser Particle Counter, Viable Air Sampler, Microscope, MilliFlex OasisTest System, Conductivity meter, pH meter and TOC analyzer.
- Monitor temperatures of Microbiological QC equipment, such as refrigerators, freezers, and cryo-freezers.
- Read EM (Environmental Monitoring) data and document results on relevant forms and electronic systems
- Perform trending and generate trending charts for EM data.
- Perform Cleaning Verification of cleaned production equipment.
- Perform membrane filtration bioburden testing using the Milliflex system.
- Perform growth promotion testing.
- Coordinate sample shipment for various outside testing requirements.
- Maintain inventory of department supplies and place purchase orders.
- Perform visual inspection of incoming department supplies in accordance with appropriate material specifications.
- Perform bioburden testing of samples per USP, EP, and JP requirements.
- Responsible for EM out-of-limit results, such as notification, investigation assistance, re-testing of alert and action OOL’s, etc.
- Comply with all safety policies, practices, and procedures.
- Report all unsafe activities to supervisor and/or Human Resources.
- Participate in proactive team efforts to achieve departmental and company goals.
- Perform other duties as assigned.
- 5+ years of biotech industry experience within a GMP biopharmaceutical manufacturing organization. 2+ years of industry experience working with mammalian cell culture.
- Ability to apply knowledge of good manufacturing practices and good laboratory practices daily.
- The understanding and ability to perform aseptic and relevant microbiological techniques such as microbial isolation, streak plate and gram staining.
- Ability to follow gowning practices for cleanroom environments.
- Ability to exercise judgment within defined procedures and practices to determine appropriate action.
- Bachelor’s degree (B.A.) or equivalent from four-year college or university, preferably in Microbiology or a relevant life sciences discipline.
- 2+ years of related experience and/or training; or equivalent combination of education and experience.
- 2+ years of industry experience working with mammalian cell culture.
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