Integra LifeSciences Director, International Program Management (Work remotely w/Travel) in Mansfield, Massachusetts

Overview

Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in orthopedic extremity surgery, neurosurgery, reconstructive and general surgery, and regenerative wound care.

Integra's orthopedic products include devices and implants for foot and ankle, hand and wrist, shoulder and elbow, tendon and peripheral nerve protection and repair. Integra is a leader in neurosurgery, offering a broad portfolio of implants, devices, instruments and systems used in neurosurgery, neuromonitoring, neurotrauma, and related critical care. Integra’s Tissue Technologies is an in-patient and outpatient Regenerative product portfolio, which includes products for wound care, burns, abdominal reconstruction, and plastic & reconstructive surgery. In the United States, Integra is a leading provider of surgical instruments to hospitals, surgery centers and alternate care sites, including physician and dental offices.

Founded in 1989 Integra is headquartered in Plainsboro, New Jersey and has over 4,500 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol "IART.

Responsibilities

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

  • Liaise with cross-functional stakeholders (e.g., International Commercial Leaders for prioritization, Product Development for Testing and R&D support, and Clinical for Clinical Strategy, QA for required Quality certifications etc.) to drive the execution of complex registrations and registration amendments projects.

  • Establish a clear process for vetting/approval of registration requests and provide long-term vision of project schedules, identifying and mitigating potential risks

  • Implement procedures, policies, and technologies to develop and add definition and consistency to project management function (Project Management SOP’s or guidance documents)

  • Provide mentoring for project managers, including communication, technical, and interpersonal skills critical to successfully managing projects and people

  • Resolve discrepancies and manage conflicts between competing priorities

  • Manage project management resources to maximize the project work that can be accomplished in conjunction with the divisional priorities

  • Track and document project successes, failures, and lessons learned across projects to continuously improve the project management function

  • Administrative work associated with direct reports, as required

Qualifications

The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.

  • Bachelor’s degree in science, engineering or medical device science related discipline from an accredited university or college. Advanced degree(s) in Business Administration or related engineering discipline(s) preferred.

  • A minimum of 7+ years of Project Management experience in a highly regulated product development enviornment, operating within Design Control procedures, preferably from within the medical device industry.

  • Demonstrated aptitude for successfully managing multiple projects, of varying complexity, within the specified guidelines, timeframes and budgets.

  • Experience managing direct reports

Vacancy ID 2018-27468

Location US-MA-Mansfield

Position Type Regular Full-Time

Category Regulatory Affairs