Integra LifeSciences

  • Sr. Production Supervisor

    Vacancy ID
    Position Type
    Regular Full-Time
  • Overview

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    • Responsible for directing the daily production activities, QC in-process inspection and staff in the Crosslink, Packaging, Boxing areas in support of multiple product lines.
    • Ensure daily production goals are met and report production line progress at shift meetings.
    • Ability to operate, maintain, troubleshoot process equipment, and make minor adjustments as needed. Send plant alerts for situations that cannot be triaged or resolved.
    • Responsible for completing all Oracle transactions during shift.
    • Accurately maintain all entries into all required logs, log books and records pertaining to Crosslink, Packaging, Boxing and other work-in-progress related (WIP)activities.
    • Responsible for maintaining process and component inventories. Place Purchase Requisitions for general processing supplies.
    • Support any Non-Conformance/CAPA/Audit related investigations.
    • Responsible for maintaining legible and accurate records and other procedures to comply with regulatory requirements, Good Manufacturing Practices (Quality Systems Regulations) and Standard Operating Procedures.
    • Plan and lead manufacturing process improvements, and other Lean initiatives to optimize performance and drive short-term and long-term business improvements.
    • Support and participate in cross-functional teams.
    • Coach, counsel, train and motivate staff – provide clear direction and oversight of staff in effectively carrying out their daily responsibilities.
    • Perform administrative duties (e.g. review and approve timecards, overtime, absenteeism reports, place purchase requisitions, maintain training records, etc.)
    • Maintain a clean and orderly work area, and perform all work in compliance with Good Manufacturing Practices (Quality Systems Regulations), and Standard Operating Procedures, and Health and Safety requirements.
    • Interface with QA and to interface with the Materials Management Department to ensure efficient flow of materials through operations.
    • Responsible for the QC in-process inspection process of product
    • Maintenance of appropriate conditions of all in-process quarantine locations
    • Coordinate and inform other departments of inspection and/or testing status in support of production and project goals and initiatives
    • Assist in the review and disposition of non-conforming material
    • Maintain records of inspection and all testing performed on the appropriate test records
    • Perform line clearances and quality reviews in manufacturing, labeling or other assigned areas during manufacturing activities.
    • Provide QC support to various departments as needed {e.g. QA, Engineering, Product Development, etc.
    • Demonstrate safe behavior and support department/plant Safety goals in a continuous improvement process.
    • Perform other related duties as expected.
    • Works with Manufacturing Engineering and Product Development to improve yield and reduce scrap.


    • Bachelor's degree in a relevant discipline or equivalent professional experience
    • Minimum 3 years of experience in the medical device industry in a supervisory role.
    • Demonstrated organizational and communication skills.
    • Must possess strong leadership skills
    • Possess team-focused attitude and work in team oriented environment.
    • Clean room experience highly desirable
    • Demonstrated knowledge of FDA and ISO regulations and standards.
    • Demonstrated computer skills. Must be capable of working in an Oracle Enterprise Resource Planning (ERP) system. Database and quality data reporting experience required.
    • Fundamental understanding of mathematics and chemistry.
    • Experience with process equipment is necessary, to operate, maintain, train and analyze problem
    • Able to gown in surgical scrubs and clean room clothing
    • Able to work overtime as required


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