Global Technical Manager – Sterilization

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SGS

10,000+ employees

Founded 1878

📋 Compliance

☁️ SaaS

Compliance • SaaS • Sustainability

SGS is the world's leading Testing, Inspection, and Certification (TIC) company, providing a comprehensive range of services designed to assure quality and integrity across various sectors. SGS is focused on sustainability, offering climate action services and an all-encompassing ESG portfolio under its IMPACT NOW suite. The company has ambitious targets for growth by 2027, driven by its strategy to address global megatrends. SGS operates globally, providing business assurance, connectivity and products, digital trust, health and nutrition, and solutions for industries and the environment.

📋 Description

• Oversee sterilization processes within medical devices and provide technical support related to sterilization across all certification schemes • Act as line manager and lead the team of MDR Product Assessors-Sterilization • Provide technical advice in relation to sterilization to support all stages of the medical device conformity assessment process • Establish competence criteria, update, deliver and maintain appropriate training packages for Product Assessors • Develop, maintain and implement sterilization QMS documentation related to medical devices conformity assessment process • Manage the development and implementation, including approval process for Product Assessors and sterilization auditors • Monitor, analyse, and report team performance, implementing timely corrective actions and providing regular updates to the Head of Operations

🎯 Requirements

• More than 10 years in the Medical device industry (at least 5 years within sterile medical device research and development and/or manufacturing) • 5 years as a MDR and/or IVDR medical device Lead Auditor / Product Assessor – Sterilization within a Notified Body • 2 years of experience in a leadership role • Good working knowledge of medical device management systems, medical device compliance and auditing and technical documentation assessment techniques • Appropriate knowledge and understanding of devices legislation as well as harmonised standards, CS and guidance documents in regards to sterilization • Appropriate knowledge and understanding of the conformity assessment procedures provided for in the regulations for medical devices • Experience supporting or leading global or cross‑functional teams.

🏖️ Benefits

• Flexible schedule and hybrid model • SGS university and Campus for continuos learning options • Benefits platform

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