Quality Control Microbiologist II

Anika; Bedford (MA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Discretionary bonus

Comprehensive healthcare benefits

Health Savings Account (HSA)

401(k) with company match

Employee stock purchase plan (ESPP)

Paid time off

Long-term incentives including stock

Job summary

Anika is seeking a QC Microbiologist II to perform routine and complex microbiology testing of materials, in-process samples, and finished products. You will conduct environmental monitoring in ISO 5–8 areas and support aseptic manufacturing operations with strong data integrity.

The role requires independent work under cGMP, adherence to USP/EP/JP pharmacopeia, and collaboration with QA, Manufacturing, and cross-functional teams in a regulated setting.

Qualifications

• Bachelor's degree in Microbiology or related field.
• 2+ years of hands-on experience in a cGMP QC Microbiology lab.
• Experience in classified cleanrooms (ISO 5–8) and EM support.

Responsibilities

• Perform routine and non-routine microbiology testing on materials and products.
• Conduct environmental monitoring in ISO cleanrooms and support media fills.
• Maintain accurate, real-time documentation in LIMS and SOP adherence.
• Support investigations for environmental excursions and deviations.
• Assist with SOPs, test methods, and regulatory readiness.

Skills

Communication skills

Analytical skills

Independent work

Detail-oriented

Education

Bachelor's degree in Microbiology or related field

Tools

LIMS/eQMS systems

BET/LAL software

Bioburden filtration apparatus

Job description

What You’ll Do

The QC Microbiologist II performs routine and complex microbiological testing of raw materials, in-process samples, finished products, and critical utilities. This role plays a critical part in maintaining environmental control by conducting Environmental Monitoring (EM) of classified cleanrooms and providing direct microbiology and EM support during aseptic process simulations (media fills) and routine commercial fill-finish manufacturing operations. The QC Microbiologist II 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

• Performs routine and non-routine testing on raw materials, in-process samples, final drug products, and critical utilities, including Purified Water, Water for Injection, Compressed Air, and Nitrogen.


• 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.


• Conducts utility sampling including critical water system loops such as Purified Water and WFI.


• Incubates and enumerates environmental samples, performs preliminary identification of isolates, and supports trending of environmental data for periodic reporting.


• Provides dedicated EM coverage during Aseptic Process Simulations (Media Fills) and commercial fill-finish manufacturing runs.


• Executes critical monitoring including active air, passive settle plates, surface sampling, and personnel gown monitoring inside Grade A / ISO 5 critical zones.


• Performs personnel qualification and re-qualification for aseptic gowning for manufacturing and laboratory staff.


• Monitors operator adherence to aseptic technique and cleanroom behaviors during operational runs; escalates and documents discrepancies immediately.


• Initiates and 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

This role is responsible for performing microbiological testing and environmental monitoring activities that directly support the quality and sterility assurance of pharmaceutical and medical device products. The position requires the ability to work independently with minimal supervision while following established procedures and regulatory requirements. Success in this role requires strong technical knowledge of QC Microbiology testing, environmental monitoring, aseptic processing, and data integrity, along with 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 <61>, <62>, <71>, <85>, and <1116>, 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.

The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

Onsite