Manager, Quality Compliance

The Manager, Quality Compliance role at Integra LifeSciences is responsible for directing all activities of the Quality Management System. The position ensures that the company's medical‑device and pharmaceutical operations meet the required Quality, Environmental, Health & Safety policies and regulatory standards while supporting the broader mission of improving healthcare outcomes. Day‑to‑day duties include leading the medical‑device complaint process, from triage and investigation to root‑cause analysis and risk assessment, and guaranteeing that complaints are closed within set timelines. You will also manage the site's internal audit programme, create the annual audit schedule, assign qualified auditors, and follow up on findings and corrective actions. Additional responsibilities cover maintaining the Learning Management System, overseeing document control within the PLM environment, driving the CAPA process, and contributing to management reviews and quality objectives. The role further involves coaching a multidisciplinary team of Quality Engineers and Technicians, allocating resources, and promoting a culture of continuous improvement across the site. The position requires a Master's degree in a Life Sciences discipline and at least ten years of professional experience in medical‑device or pharmaceutical manufacturing. Candidates must possess thorough knowledge of medical‑device standards and regulations, including ISO 13485, EU MDR, 21 CFR Part 820 and related international requirements. Fluency in both English and French is mandatory, as is strong leadership capability with experience supervising laboratory teams. Excellent communication, organizational, negotiation and interpersonal skills, together with solid analytical and problem‑solving abilities, are also essential. The ability to collaborate effectively with management across multiple sites and functions is required. While the description does not list specific benefits or location details, the role offers the chance to work within a global organization that values innovative thinking and a proactive quality culture. You will be part of a large, diverse workforce of more than 4,000 employees, contributing to projects that shape the future of healthcare and drive operational excellence. What the role asks for: - Master's degree in Life Sciences - 10 years experience in medical‑device/pharma manufacturing - Knowledge of ISO 13485, EU MDR, 21 CFR Part 820 and other regulations - Fluent in English and French - Strong management and leadership, supervising lab teams - Excellent communication, organizational and negotiation skills - Strong analytical and problem‑solving abilities - Ability to collaborate across multiple sites and functions