Quality Compliance Manager, ECMP Site Facilitator

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. Quality Compliance Manager, ECMP Site Facilitator Provides tactical support and oversight of the implementation of the Enterprise Compliance Master Plan at Integra LifeSciences sites. Responsibilities include developing individual site project plans derived directly from the Enterprise Compliance Master Plan (ECMP), ensuring project plans are implemented according to the defined timeline, and working closely with existing site Quality and Operations leaders. May have responsibility for more than one site. Will be traveling between our three (3) sites as needed: Añasco, Puerto Rico; Mansfield, MA; Cincinnati, OH occasionally. Primary location is Mansfield, MA. Key Responsibilities Develop and manage sites’ project plans for implementation of ECMP workstream outputs. Track progress and ensure execution according to plan. Report sites’ progress to ECMP Program Management Office (PMO). Be responsible for ECMP documentation and schedule at sites. Coordinate collaborative activities between sites’ local activities. Periodically review the outputs from the sites’ workstream activities to ensure alignment with requirements of the ECMP and individual site’s project plan. Facilitate resolution of issues. Other duties as assigned. Requirements Bachelor's degree required (Engineering, Science or closely related technical discipline preferred). 10+ years of experience leading a team (indirect reports and/or projects) or equivalent education and years of management experience. Experience working Quality Management Systems and understanding compliance. Experience in medical device industry required, including material remediation experience. Experience in implementing remediation programs, and working with compliance frameworks such as FDA, ISO 13485, and EU MDR. Demonstrated management and communication skills; proven track record of cross‑functional collaboration across teams and change management skills. Strong attention to detail. Strong communication and presentation skills, with the ability to articulate program status and risks to key stakeholders. Ability to travel up to 50% as needed based on site needs; regular on‑site presence at designated facilities within scope of responsibilities. Residence requirement: Mansfield, MA. Tools and Equipment Used Ability to utilize a computer, telephone, smartphone as well as other general office equipment. Strong computer skills required. Physical Requirements The physical requirements listed in this section include, but are not limited to, the motor/physical abilities and skills required of the position to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position. Adverse Working Conditions There are no adverse working conditions associated with this position. Salary Pay Range

$109,250.00 - $149,500.00 USD.

Benefits Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in 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)). Equal Employment Opportunity Statement 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. This site is governed solely by applicable U.S. laws and governmental regulations. If you have difficulty using our online system due to a disability and need an accommodation, please email us at View email address on click.appcast.io. #J-18808-Ljbffr Integra LifeSciences