Quality Control Microbiologist

ANIKA-GCC; Bedford (MA); On-site; USD 66,000 - 82,000; Full time

Benefits offered by this job

Bonus program

Healthcare benefits

Health savings account

401(k) match

Employee stock purchase plan

Paid time off

Stock awards

Job summary

Anika in Bedford, MA is seeking a QC Microbiologist to support GMP manufacturing with microbiological testing, environmental monitoring, and validation activities. You will ensure regulatory compliance, document test results, and collaborate with Engineering and R&D on process validation and new product introductions.

The role requires a Bachelor’s degree in Microbiology or related field, 1 year of pharma testing experience, and strong documentation skills.

Qualifications

• This role requires a Bachelor’s degree in Microbiology or related field or equivalent experience.
• Minimum 1 year of pharmaceutical or regulated industry microbiological testing experience.
• Experience with sterility, bioburden, endotoxin, microbial ID, gram staining, and water testing.
• Knowledge of GMP, GLP, FDA regulations, and ISO requirements.
• Excellent written and verbal communication and documentation skills.

Responsibilities

• Perform microbiological testing for raw materials, in-process samples, and finished products.
• Support environmental monitoring in classified cleanroom environments.
• Review and maintain validation protocols and reports.
• Collaborate with Engineering and R&D on process validation and new product introduction.
• Maintain laboratory records, data integrity, and compliance with SOPs.

Skills

Communication skills

Attention to detail

Documentation and data integrity

Project/time management

GMP/GLP knowledge

Team collaboration

Education

Bachelor's degree in Microbiology

Equivalent experience considered

Tools

Microsoft Office

Job description

Job Description

The QC Microbiologist performs microbiological testing and validation activities supporting commercial manufacturing operations under GMP conditions, ensuring compliance with regulatory requirements, product quality standards, and environmental monitoring programs. In this role, you serve as a subject matter expert in microbiological testing, environmental monitoring, and validation activities for sterile manufacturing processes and systems.

• Perform microbiological testing including bioburden, sterility, endotoxin, microbial identification, gram staining, bacteriostasis, and growth promotion assays for raw materials, in-process samples, bulk products, finished products, and stability samples.
• Conduct purified water and DI water testing, including bioburden, endotoxin, membrane filtration, and TOC testing in accordance with USP requirements.
• Complete laboratory documentation, test records, and related activities in compliance with SOPs, GMPs, and data integrity requirements.
• Support development, qualification, and validation of microbiological methods, including new product sterility and endotoxin testing methods.
• Author, execute, review, and approve validation protocols and reports related to microbiological methods, autoclaves, depyrogenation ovens, and related systems.
• Collaborate with Engineering and R&D to support process validation, equipment validation, and new product introduction activities.
• Review environmental monitoring results for classified cleanroom areas, maintain environmental monitoring databases, and summarize data for annual environmental reports.
• Support environmental monitoring programs and provide guidance and training on environmental compliance practices.
• Verify laboratory testing performed by technicians and assist in onboarding and technical training activities.
• Establish and maintain databases for microbiological testing and validation data.
• Participate in internal audits and support regulatory inspections and audit readiness activities.
• Perform other duties and projects as assigned.

What It Takes

This role requires the ability to work on complex microbiological and validation assignments requiring detailed analysis, sound scientific judgment, and strict adherence to GMP and regulatory requirements. The position exercises initiative and independent decision-making within established procedures and quality systems. Success in this role requires strong technical expertise in microbiological testing and environmental monitoring, attention to detail, effective problem-solving skills, and the ability to manage testing priorities and reporting timelines in a regulated manufacturing environment.

What You Bring

• Bachelor’s degree in Microbiology, Biology, or related scientific discipline; equivalent experience may be considered.
• Minimum of 1 year of pharmaceutical or regulated industry experience performing microbiological testing.
• Hands-on experience with sterility, bioburden, endotoxin (LAL), microbial identification, gram staining, purified water testing, bacteriostasis, and growth promotion assays.
• Experience supporting validation activities, including new product validation, microbiological method validation, and equipment validation.
• Knowledge of GMP, GLP, FDA regulations, and applicable ISO requirements.
• Experience supporting environmental monitoring programs within classified cleanroom environments.
• Excellent written and verbal communication skills.
• Demonstrated ability to manage testing schedules, meet reporting deadlines, and maintain accurate documentation.
• Proficiency with Microsoft Office Suite, including Word, Excel, and PowerPoint.

Nice to Have

• Experience with aseptic processing environments and media fill evaluations.
• Familiarity with autoclave and depyrogenation oven validation activities.
• Experience maintaining environmental monitoring trending databases and generating annual reports.
• Prior experience supporting internal audits or regulatory inspections.
• Knowledge of USP microbiological testing requirements and contamination control principles.

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.

Benefits:

• 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
• 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.

Employment Type: Full-time

Location: Bedford, MA

Salary Range: $66,000 – $82,000