Regulatory Compliance Lead

vor 1 Tag


Le Locle, Neuenburg, Schweiz Integra Lifesciences Switzerland SAS Vollzeit
About the Role

We are seeking an experienced Compliance Supervisor to join our team at Integra Lifesciences Switzerland SAS. As a key member of our quality assurance department, you will play a vital role in ensuring the highest standards of quality and compliance across our operations.

In this challenging and rewarding role, you will be responsible for managing a team of complaint technicians, overseeing daily activities, and ensuring that all tasks are completed on time and to the required standard. You will also be expected to implement and manage complaints procedures, investigate trends, and provide quality support to production and open projects/initiatives.

To succeed in this position, you will require a Bachelor's Degree in a related technical discipline and a minimum of 5 years of professional work experience in a quality assurance or compliance audit environment. Experience in a Medical Device manufacturing environment is highly desirable, as is fluency in both French and English.

As a Compliance Supervisor, you will be working closely with various teams, including Design Quality Assurance, Medical Safety, Product Development, and Post market Surveillance. Your ability to interface with internal and external customers, as well as your knowledge of statistical techniques, Agile, Oracle, EtQ, Minitab, Trackwise, and Microsoft office tools, will be invaluable assets in this role.

Main Responsibilities:

  • Team management and supervision
  • Complaints procedure implementation and management
  • Trend analysis and investigation
  • Quality support to production and open projects/initiatives
  • Health Hazard Evaluation and risk analysis
  • Post Market Surveillance activities

Requirements:

  • Bachelor's Degree in a related technical discipline
  • Minimum of 5 years of professional work experience in quality assurance or compliance audit environment
  • Experience in a Medical Device manufacturing environment preferred
  • Fluent in French and English
  • Knowledge of Medical device standards and regulations
  • Strong management skills
  • Excellent communication, organizational, negotiation, and interpersonal skills

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