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　　SUMMARY

　　Qualified candidates must possess relevant experience as a Microbiologist in one or more of the following areas and be considered a Subject Matter Expert in a minimum of one area:

　　Controlled environment monitoring

　　Water system monitoring

　　Bacterial endotoxin test method validation and monitoring

　　Bioburden test method validation and monitoring

　　Ethylene oxide sterilization validation

　　Responsibilities for this position are directly associated with microbiological testing, monitoring, and sterility assurance used in medical device manufacturing. The candidate must have experience interpreting and applying standards and regulations to medical device microbiological and sterility assurance control programs for the purposes of interpreting data, implementing procedures, and remediation projects. Candidate must possess sufficient knowledge and experience to serve as a subject matter expert within one or more of the areas listed above. The candidate must be a team player who thrives in a collaborative environment but also has the capability to work autonomously. An understanding of clean room practice/cGMP and laboratory/GLP environments is required. The qualified candidate must understand the concepts of risk management as it relates to microbial monitoring and sterility assurance in a medical device manufacturing environment.

　　This position reports to Corporate Quality Microbiology and Sterilization but will be located on-site in our Boston manufacturing facility.

　　RESPONSIBILITIES

　　Generation and execution of microbial method validation protocols and reports including the writing, routing and approval of summary documentation.

　　Design experimental plans to address specific laboratory issues as needed.

　　Manage sample/testing processing with onsite and third-party labs, ensure timely testing and result reporting.

　　Ensure compliance of microbiology procedures, validations, and records with all company policies and procedures and appropriate regulations, including FDA and ISO 9001, ISO 13485, AAMI ST72, ISO 11737, ISO 14644, ISO 14698, ISO 11135, CMDR, Medical Device Directive, and USP.

　　Interpret microbiological data in order to identify trends and issues that require investigation.

　　Contribute to risk management activities including PFMEA generation.

　　Scheduling coordination, material allocation and alignment of personnel in order to successfully complete project assignments.

　　Create procedures for microbiological testing and sampling in alignment with validations and in compliance with applicable regulations.

　　Mentors non-senior level microbiology staff.

　　Serve as Microbiology representative on cross-functional teams for transfer, NPI, and other projects as necessary including supervision of contract resources.

　　Experience with Controlled environment monitoring, Water system monitoring, compressed air monitoring, Bacterial endotoxin test method validation, and monitoring, Bioburden test method validation and monitoring, and ethylene oxide sterilization preferred.

　　Ensure that all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO or other applicable requirements.

　　Support and address comments and suggestions associated with sterilization and microbiological test method validations and monitoring procedures.

　　Change control, non-conformance, and CAPA support.

　　Participate in FDA inspections, ISO certifications, surveillance audits and customer audits.

　　DESIRED MINIMUM QUALIFICATIONS

　　Bachelor degree or equivalent with 5+ years of experience, Master degree with 3+ years of experience, Doctoral degree with 0-2 years of experience

　　Demonstrates excellent organizational and communication skills.

　　Results-oriented with a strong focus on quality principles.

　　Excellent technical writing skills with an understanding of good documentation practice.

　　Experience conducting microbial test method validations and managing projects independently.

　　Experience creating and changing procedures used in operations for microbiological monitoring of the environment and products.

　　Working knowledge of applicable microbiology standards including, but not limited to, AAMI ST72, ISO 11737, ISO 14644, ISO 11135, and USP.

　　Ability to track milestones and manage projects.

　　Working knowledge of applicable regulations and their interpretation within the industry.

　　Integra 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.

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