Quality Control Microbiologist II

What You’ll Do

• Performs routine and complex microbiological testing of raw materials, in-process samples, finished products, and critical utilities.
• Conducts Environmental Monitoring (EM) of classified cleanrooms and provides direct microbiology and EM support during aseptic process simulations (media fills) and routine commercial fill-finish manufacturing operations.
• Operates with minimal supervision under cGMP regulations, adhering strictly to USP/EP/JP pharmacopeial requirements, standard operating procedures (SOPs), and data integrity standards.

How You’ll Contribute

• Executes standard assays including Bioburden Testing using membrane filtration and direct plating, Bacterial Endotoxin Testing (BET/LAL) kinetic assays, Sterility Testing using isolator/cleanroom hood environments, Microbial Identification, and Growth Promotion Testing on media lots.
• Maintains accurate, real-time documentation in laboratory notebooks, logbooks, and LIMS in strict compliance with cGMP and Data Integrity principles (ALCOA+).
• Performs routine cleanroom monitoring across ISO 5, ISO 7, and ISO 8 classified areas, including viable active air, non-viable particulates, surface/contact plates, and personnel monitoring.
• Executes critical monitoring including active air, passive settle plates, surface sampling, and personnel gown monitoring inside Grade A / ISO 5 critical zones.
• Supports investigations for Environmental Excursions, Out-of-Specification (OOS), Out-of-Trend (OOT), and process deviations using root cause analysis tools.
• Authors and revises Standard Operating Procedures (SOPs), test methods, validation protocols, and reporting templates.
• Supports audits and inspection readiness for internal QA, FDA, EMA, and regulatory inspections, as well as facility re-qualification and validation activities.

What It Takes

• Strong technical knowledge of QC Microbiology testing, environmental monitoring, aseptic processing, and data integrity.
• Sound judgment, attention to detail, and the ability to work effectively in a highly regulated manufacturing environment.

What You Bring

• Bachelor’s degree (B.S.) in Microbiology, Biology, or a closely related biological science discipline.
• 2+ years of hands-on experience in a cGMP Quality Control Microbiology laboratory within the pharmaceutical, biopharmaceutical, or medical device industry.
• Demonstrated experience working inside classified cleanrooms (ISO 5–8) and providing direct microbiology and EM support for aseptic manufacturing or fill-finish operations.
• Proficiency with USP/EP/JP pharmacopeia, including USP , , , , and , and cGMP/FDA/EMA regulatory guidelines.
• Experience with BET/LAL kinetic software, particle counters, bioburden filtration apparatus, automated microbial identification systems, and LIMS/eQMS systems.
• Strong understanding of microbiological testing, environmental monitoring, aseptic processing, contamination control, and applicable laboratory practices.
• Strong verbal and written communication skills with the ability to accurately document technical information and communicate effectively with Quality, Manufacturing, and other cross-functional teams.
• Strong analytical, organizational, and problem-solving skills with the ability to work independently and manage multiple priorities.
• Ability to gown fully in aseptic cleanroom suit assemblies, including hoods, goggles, masks, boots, and double-gloves, and remain in classified environments for extended periods of 4+ hours.
• Ability to lift up to 25 lbs., maneuver sampling equipment, and perform repetitive laboratory tasks including pipetting, plate streaking, and membrane filtration.
• Willingness to support manufacturing schedules, which may include occasional weekend, evening shift, or holiday coverage.

Nice to Have

• Experience supporting Aseptic Process Simulations (Media Fills) and commercial fill-finish manufacturing operations.
• Experience with environmental monitoring in Grade A / ISO 5 critical zones.
• Experience performing personnel gowning qualification and re-qualification.
• Experience supporting environmental monitoring trending, facility re-qualification, or validation activities.
• Experience with electronic Quality Management Systems and laboratory information management systems.

The salary range provided is based on the Company’s reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life.