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INTEGRA LIFESCIENCES CORP
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Quality Compliance Manager - ECMP Site Facilitator(m/w/x)

Le Locle, Rietheim-Weilheim
Full-timeOn-siteSenior

Description

As a Quality Compliance Manager and ECMP Site Facilitator, you will oversee the implementation of compliance plans across multiple sites, ensuring projects stay on track and meet established timelines. You will collaborate with local teams to resolve any issues that arise.

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Requirements

  • •Bachelor's degree in Engineering, Science, or related technical discipline
  • •10+ years of experience leading a team or equivalent education and management experience
  • •Experience working with Quality Management Systems and compliance
  • •Experience in highly regulated industries, medical device and/or pharmaceutical preferred
  • •Experience in implementing remediation programs and compliance frameworks such as FDA, ISO 13485, and EU MDR
  • •Demonstrated management and communication skills
  • •Strong attention to detail
  • •Strong communication and presentation skills
  • •Ability to travel up to 50% if needed
  • •Strong computer skills

Education

Bachelor's degree

Work Experience

10 years

Tasks

  • •Develop and manage project plans for ECMP implementation
  • •Track progress and ensure execution according to the plan
  • •Report site progress to the ECMP Program Management Office
  • •Manage ECMP documentation and scheduling at sites
  • •Coordinate collaborative activities between local site teams
  • •Review outputs from site work stream activities for alignment with ECMP requirements
  • •Facilitate resolution of issues
  • •Perform other assigned duties

Tools & Technologies

FDAISO 13485EU MDR

Languages

English – Business Fluent

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