Director, Quality Microbiology

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.SUMMARYThe Director, Quality Microbiology, is responsible for leading Integra LifeSciences operational microbiology teams across the Tissue Technologies and Codman Surgical Specialties businesses. Qualified candidates must possess relevant experience with Subject Matter Expertise in the following areas:• Controlled environment qualification and monitoring• Water system qualification monitoring• Bacterial endotoxin test method validation and monitoring• Bioburden test method validation and monitoring• Contamination control systems (monitoring, gowning, aseptic techniques, cleaning, etc.)The candidate must be an experienced team leader who leverages the talent of their team to increase performance, generate results, and maintain robust quality of manufacturing site microbiology programs. This position reports to Corporate Quality Sterility Assurance and will be located in Princeton or another Integra facility with flexibility for travel as needed.ESSENTIAL DUTIES AND RESPONSIBILITIESTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily:Provide technical talent training, mentoring, and development support for microbiology personnel and cross-functional teamsServe as a representative for microbiology globally and collaborate across functions such as quality, operations, R&D, Global Supply, Finance, Sales, and Marketing to ensure company goals are metAct as a global process owner for microbiology and oversee the implementation of Global procedures to support compliance of Integra LifeSciences manufacturing site Microbiology Quality programsCreate and sustain long-term strategies and advise a team of managers and scientists across the Quality Microbiology teamProvide leadership and direction to the Quality Microbiology team to ensure business, quality, and compliance objectives are metReport results of site microbiology programs to leadership for projects and key performance indicatorsResource business projects such as manufacturing transfer, acquisitions, new product development, etc. with microbiology personnelParticipate as a microbiology SME in internal audits, and external audits such as FDA inspections, ISO certifications, surveillance audits and customer audits.Maintain a strong working knowledge of standards and regulations including FDA CFR, ISO 13485, AAMI ST72, ISO 11737, ISO 14644, ISO 14698, ISO 22442, CMDR, Medical Device Directive, and USP.DESIRED MINIMUM QUALIFICATIONSThe requirements listed below are representative of the knowledge, skill, and/or ability required for this positionREQUIRED EXPERIENCEBachelor’s, or preferably Master of Science degree, in Microbiology or similar discipline.Minimum 12 years’ experience in medical device or regulated industry with 5 years of leadership experience, with experience in microbiology.PREFERRED EXPERIENCEExperience working with the manufacturing of tissue-based products and surgical tools as a microbiologist or similar scientific discipline in the medical device industryExperience leading teams in the development and implementation procedures used in operations across multiple businesses/manufacturing sites.Advanced communication skills (written and verbal) with the ability to curate information to a diverse audience of stakeholdersRobust cross-functional collaboration skillset with the capability of driving quality and operational excellenceAdvanced team leadership experience including mentoring, meeting facilitation, coaching, influencing, and negotiationCapable of working autonomously and with independence when needed while maintaining strong performanceDemonstrated capability to develop strategic direction, goals, and guiding execution in a team-based working environmentAdvanced experience working within Quality Systems including, but not limited to, change control, CAPAs, deviations, nonconformances, risk assessmentsDirect experience representing a department in regulatory inspections and communicationsAdvanced technical writing skillset with the capability to interpret and author complex documentationWorking knowledge of applicable microbiology standards including, but not limited to, FDA CFR, ISO 13485, AAMI ST72, ISO 11737, ISO 14644, ISO 14698, ISO 22442, CMDR, Medical Device Directive, and USP.Ability to travel up to 25%.Salary Pay Range:$166,750.00 - $228,850.00 USD SalaryOur 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 LifeSciencesIntegra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:EEO Is the Law | EOE including Disability/Protected VeteransIntegra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at View email address on us.fitly.work Agency SubmissionIntegra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate’s name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.Integra - Employer Branding from Integra LifeSciences on VimeoSummaryLocation: US-NJ-Princeton-100-Headquarters; US-NJ-Plainsboro-105-Facility; US-MA-Mansfield-190-Facility; US-UT-West Valley-106-Facility; US-OH-Cincinnati-114-Facility; US-PR-Anasco-165-Facility; US-MD-Columbia-NA-Facility; US-MA-Braintree-220-Facility; US-CA-Irvine-NA-Facility; US-IN-Lafayette-NA-Facility; US-TN-Cordova-183-FacilityType: Full time