Quality Compliance Manager, ECMP Site Facilitator

Integra LifeSciences Holdings Corp.-posted about 1 month ago
Full-time • Manager
Braintree, MA
1,001-5,000 employees
Miscellaneous Manufacturing
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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. The Quality Compliance Manager, ECMP Site Facilitator, provides tactical support and oversight of the implementation of the Enterprise Compliance Master Plan at Integra LifeSciences sites. They are responsible for to developing individual site project plans derived directly from the Enterprise Compliance Master Plan (ECMP), and ensuring that the project plans are being implemented according to the defined timeline and plan. Site Facilitators will work closely with existing site Quality and Operations leaders and may have responsibility for more than one site.

  • Developing and managing sites' project plans for implementation of ECMP workstream outputs
  • Tracking progress and ensuring execution according to plan
  • Reporting sites' progress to ECMP Program Management Office (PMO)
  • Being responsible for ECMP documentation and schedule at sites
  • Coordinating collaborative activities between sites' local activities
  • Periodically reviewing the outputs from the sites' work stream activities to ensure it is aligned with requirements of the ECMP and individual site's project plan
  • Facilitating resolution to issues
  • Other duties as assigned.
  • Bachelor's degree is required, (Engineering, Science or closely related technical discipline is 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 highly regulated industries required, medical device and/or pharmaceutical preferred, 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 skills
  • Strong communication and presentation skills, with the ability to articulate program status and risks to key stakeholders.
  • Ability to travel up to 50% if needed based on site needs. Regular on-site presence at designated facilities within scope of responsibilities.
  • medical
  • dental
  • vision
  • life insurance
  • short- and long-term disability
  • business accident insurance
  • group legal insurance
  • savings plan (401(k))
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