Integra LifeSciences

Limiting Uncertainty For The Busiest Surgeons

Medical Equipment Manufacturing

Repair and Regenerate Tissue, surgical instruments, neurosurgical products and advanced wound care products


Princeton, New Jersey

Company Size

3,000+ employees


neurosurgery, neurosciences, surgical instruments, collagen, and regenerative medicine

Integra LifeSciences, a world leader in medical technology with headquarters in Princeton, New Jersey, was founded in 1989 with the acquisition of an engineered collagen technology platform used to repair and regenerate tissue. Since then, Integra has expanded its base regenerative technology product portfolio to include surgical instruments, neurosurgical products and advanced wound care products, through global acquisitions and development of new and innovative products and technologies to address unmet patient needs and improve outcomes. Integra is a global leader in neurosurgery and offers a broad portfolio of products and solutions for dural access and repair, cerebral spinal fluid management and neuro-critical care. Our regenerative tissue technologies include products that address soft tissue, nerve and tendon repairs and for the treatment of acute and chronic wounds, burns, as well as for plastic and reconstructive surgery. The company has offices, manufacturing and research facilities in Asia, Australia, Europe, Middle East, and the Americas

The Opportunity

Finished Goods Assembly Supervisor

Boston, MA
  • Overview

    Integra LifeSciences is a global leader in regenerative technologies and neurosurgical solutions dedicated to limiting uncertainty for clinicians, so they can focus on providing the best patient care.

    Founded in 1989, Integra develops, manufactures, sells and supplies best-in-class products to regenerate tissue, remove brain tumors, prevent infection and much more. And over the last three decades, we’ve evolved into one of the world’s leading global medical technology companies with more than 4,000 dedicated employees who deliver innovative medical technology solutions.

    But that’s just the beginning. Integra is growing at an unprecedented rate. We’re at a moment in time where the experience you’ll gain is more robust than the experience you bring. And we’re out to invest in your future because it’s the best way to maximize ours.

    At Integra, we firmly believe our people are our greatest asset and the foundation of our success. Our comprehensive Global Total Rewards program provides competitive compensation and benefits designed to keep our people healthy, motivated and engaged. Investing in our people through these programs is possible because of Integra’s ongoing commitment to our values and our shared success.

    Integra’s health as a company begins with the well-being of our people. Benefit programs vary by country, whether provided through company-sponsored insurance and programs, through statutory government programs, or a combination of both.

    Regardless of geographic location, our commitment is to offer the following, whenever possible:
    • Benefit plans that meet all local statutory requirements
    • A range of programs that reflect typical local market practices
    • An opportunity for employees to tailor benefits to their specific needs
    • Benefits that balance employee’s short-term and long-term needs

  • Responsibilities

    • Supervise Device Process Operator and/or Finished goods assembly operators.
    • Use department databases to track and manage scheduled Device production.
    • Effectively follow SOPs, policies, and ISO/QSR inventory requirement.
    • Provides direction and Guidance to intermediate and entry level Process Operators.
    • Communicate technical details of production schedule to manufacturing personnel.
    • Assist in updating SOPs as necessary.
    • Manage Production inventory levels.
    • Develop business continuity/resilience plan and methodically eliminate high risk single points of failure: people, equipment, suppliers.
    • Provide support to the Quality Team during corporate audits.
    • Actively participate in department activities and confirm compliance with controlled procedures are required.
    • Attend all scheduled production meeting.
    • Reports on all resource issues such as personnel, material, and equipment.
    • Review & transact DHR Batch Records in MAS200 and Oracle system as needed.

  • Qualifications

    • Education: An Associates/Bachelors Degree or equivalent with related work experience is required.
    • Experience: A minimum of 2-5 years’ supervisory experience in medical device, pharmaceuticals, Quality/Regulatory Compliance, or other regulated product preferred environment.
    • Familiarity with application of FDA and/or ISO quality standard in a government regulated industry.
    • Experience working in an ISO certified cleanroom and gowning requirements
    • Capable of supervising upto 15-17 direct reports while performing their own duties.
    • Moderate computer competence, including experience with database and Microsoft Office software to create reports, spreadsheets, analyze date and prepare presentations. Ability to follow instruction precisely, recognize deviation, and recommend corrective action. Detail-oriented.
    • Excellent communication and organizational skills, Strong in interpersonal skills and ability to work with others in a positive and collaborative manner.
    • Experience with Oracle and MAS200 preferred.

Building career-spanning relationships, from candidacy to organizational leadership, we provide access to the future of the Medtech and Pharma.