Senior Microbiology Technician

Senior Microbiology TechnicianJoining 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.The 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 & TestingPerform advanced microbiological testing including: Bioburden, Endotoxin, Growth Promotion TOC, Conductivity, and Utility testing (e.g., Water, Compressed Air)Conduct Environmental Monitoring of cleanrooms (viable and non-viable samples)Perform product testing of Raw Materials, In-Process samples, and Finished GoodsEnsure proper aseptic technique and adherence to GMP/GLP standards and regulationsData Analysis & TrendingReview and analyze microbiological data for accuracy and completenessSupport trending of environmental monitoring and test resultsIdentify potential adverse trends and escalate appropriatelyGenerate reports and assist in presenting findings to managementInvestigations & Quality SupportLead or support: Out-of-Specification (OOS) investigations Non-conformances and CAPAsPerform root cause analysis and recommend corrective/preventive actionsCollaborate cross-functionally (QA, Manufacturing, Engineering) to resolve quality issuesValidation & Continuous ImprovementSupport microbiological method validations and qualifications (e.g., EMPQ, utilities)Assist with implementation of new methods, systems, and process improvementsContribute to SOP development, revisions, and continuous improvement initiativesTraining & MentorshipTrain and mentor junior staff on: Testing methods Aseptic technique SOPs and compliance requirementsProvide day-to-day technical guidance and troubleshooting support in the labCompliance & Audit ReadinessEnsure compliance with FDA, ISO 13485, and other regulatory standardsAssist in preparation for and participation in: FDA inspections Internal and external auditsMaintain accurate and timely documentation in accordance with GMP requirementsLaboratory OperationsMonitor laboratory equipment and ensure proper calibration and maintenanceMaintain inventory of materials, reagents, and suppliesEnsure laboratory cleanliness and adherence to safety standardsCoordinate sample management, including send-outs to external laboratoriesAdditional ResponsibilitiesAssist in special projects and departmental initiativesSupport KPI tracking and reportingPerform other duties as assignedDesired Minimum Qualifications:Education & ExperienceBachelor's degree in Microbiology, Biology, or a related scientific field4–7 years of experience in a cGMP-regulated environment (medical device, pharmaceutical, or related industry)Technical SkillsStrong knowledge of microbiological testing methods and aseptic techniquesExperience with environmental monitoring and cleanroom operations (ISO Class 7/8 preferred)Familiarity with FDA regulations and ISO quality standardsExperience with method validation and investigation processesCompetencyStrong analytical and problem-solving skillsAbility to recognize deviations and recommend effective corrective actionsExcellent organizational and time management abilitiesEffective written and verbal communication skillsAbility to work independently and collaboratively across teamsProficiency with Microsoft Office and laboratory data systemsBehavioral & Professional ExpectationsEffective communication: Clearly conveys technical information verbally and in writing; escalates issues appropriately and collaborates cross-functionallyPrioritization & time management: Effectively manages multiple tasks, organizes workload, and consistently meets deadlines in a fast-paced QC environmentAdaptability: Demonstrates flexibility and maintains performance when priorities shift or urgent issues arise (e.g., EM excursions, investigations)Attention to detail: Ensures high accuracy in documentation, data review, and execution of test methodsProblem-solving mindset: Proactively identifies issues, proposes solutions, and supports continuous improvement initiativesAccountability & ownership: Takes responsibility for assigned work, follows through on commitments, and ensures compliance with GMP standardsTeam collaboration: Works effectively within the lab and with cross-functional teams; supports a positive, quality-focused cultureMentorship & support: Provides guidance to junior staff, reinforces best practices, and supports training and knowledge sharingSalary Pay Range:$29.86 - $40.91 USD HourlyOur salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.Additional Description for Pay Transparency:Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences