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Senior Microbiology Technician

Job in Braintree, Norfolk County, Massachusetts, 02185, USA
Listing for: Integra LifeSciences
Full Time position
Listed on 2026-07-01
Job specializations:
  • Healthcare
    Medical Science, Data Scientist
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 41135 - 56357 USD Yearly USD 41135.00 56357.00 YEAR
Job Description & How to Apply Below

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

Senior Microbiology Technician

serves as an advanced technical resource within the Quality Control Microbiology team. This role performs complex microbiological testing, supports investigations and validations, and provides day-to-day guidance to junior technicians. The position acts as a bridge between routine laboratory execution and leadership functions by ensuring data integrity, supporting process improvements, and assisting with compliance activities.

ESSENTIAL DUTIES AND RESPONSIBILITIES
  • Technical Execution & Testing
    • Perform advanced microbiological testing including:
      • Bioburden, Endotoxin, Growth Promotion
      • TOC, Conductivity, and Utility testing (e.g., Water, Compressed Air)
    • Conduct Environmental Monitoring of clean rooms (viable and non-viable samples)
    • Perform product testing of Raw Materials, In-Process samples, and Finished Goods
    • Ensure proper aseptic technique and adherence to GMP/GLP standards and regulations
  • Data Analysis & Trending
    • Review and analyze microbiological data for accuracy and completeness
    • Support trending of environmental monitoring and test results
    • Identify potential adverse trends and elevate appropriately
    • Generate reports and assist in presenting findings to management
  • Investigations & Quality Support
    • Lead or support:
      • Out-of-Specification (OOS) investigations
      • Non-conformances and CAPAs
    • Perform root cause analysis and recommend corrective/preventive actions
    • Collaborate cross-functionally (QA, Manufacturing, Engineering) to resolve quality issues
  • Validation & Continuous Improvement
    • Support microbiological method validations and qualifications (e.g., EMPQ, utilities)
    • Assist with implementation of new methods, systems, and process improvements
    • Contribute to SOP development, revisions, and continuous improvement initiatives
  • Training & Mentorship
    • Train and mentor junior staff on:
      • Testing methods
      • Aseptic technique
      • SOPs and compliance requirements
    • Provide day-to-day technical guidance and troubleshooting support in the lab
  • Compliance & Audit Readiness
    • Ensure compliance with FDA, ISO 13485, and other regulatory standards
    • Assist in preparation for and participation in:
      • FDA inspections
      • Internal and external audits
    • Maintain accurate and timely documentation in accordance with GMP requirements
  • Laboratory Operations
    • Monitor laboratory equipment and ensure proper calibration and maintenance
    • Maintain inventory of materials, reagents, and supplies
    • Ensure laboratory cleanliness and adherence to safety standards
    • Coordinate sample management, including send-outs to external laboratories
  • Additional Responsibilities
    • Assist in special projects and departmental initiatives
    • Support KPI tracking and reporting
    • Perform other duties as assigned
DESIRED MINIMUM QUALIFICATIONS
  • Education & Experience
    • Bachelor’s degree in Microbiology, Biology, or a related scientific field
    • 4–7 years of experience in a cGMP-regulated environment (medical device, pharmaceutical, or related industry)
  • Technical Skills
    • Strong knowledge of microbiological testing methods and aseptic techniques
    • Experience with environmental monitoring and cleanroom operations (ISO Class 7/8 preferred)
    • Familiarity with FDA regulations and ISO quality standards
    • Experience with method validation and investigation processes
  • Competency
    • Strong analytical and problem-solving skills
    • Ability to recognize deviations and recommend effective corrective actions
    • Excellent organizational and time management abilities
    • Effective written and verbal communication skills
    • Ability to work independently and collaboratively across teams
    • Proficiency with Microsoft Office and laboratory data systems
  • Behavioral & Professional Expectations
    • Effective communication:
      Clearly conveys technical information verbally and in writing; escalates issues appropriately and collaborates cross-functionally
    • Prioritization & time management:
      Effectively manages…
Position Requirements
10+ Years work experience
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