Company Description and Location: SGS is the world's leading testing, inspection and certification company, recognised as the global benchmark for sustainability, quality and integrity.
44,000 employees operate 2,500 offices and laboratories worldwide, enabling a safer and more interconnected world.
The role is Remote within Europe.
We are seeking a Medical Device QMS Audit Manager to lead and oversee the training, qualification, and compliance processes for QMS Auditors involved in our medical device conformity assessments.
This non-clinical role plays a vital part in ensuring the competence of technical personnel and the continued regulatory compliance of SGS Notified Body ****.
Your Mission
Lead the development and delivery of training and qualification frameworks for technical staff (excluding clinical).
Establish and maintain competence criteria, monitor qualification status, and approve audit and assessment activities.
Provide expert technical guidance across the entire conformity assessment process and contribute to the development of QMS documentation aligned with EU regulations and best practices.
Support operational, technical, and strategic initiatives to maintain the integrity and effectiveness of SGS medical device services.
Work closely with the Medical Devices Management Team to stay abreast of regulatory changes and align internal processes accordingly.
Key Responsibilities
Design and manage training programs for QMS Auditors, globally.
Approve Level 1 audits and witness audits for auditor qualification and requalification.
Contribute to recruitment, onboarding, and approval of new personnel.
Develop and maintain QMS documentation aligned with MDR, IVDR, NBOG, and MDCG guidance.
Ensure competence, compliance, and operational efficiency across assessment teams.
Provide technical support across SGS NB **** activities and contribute to business development.
Qualifications
Education: Bachelor's degree (or equivalent) in medicine, pharmacy, engineering, or related scientific field.
Experience:10+ years in the medical device industry, including at least 5 years in R&D; or manufacturing roles.
Minimum 4 years working within a Notified Body.
Minimum 2 years leadership experience.
Prior qualification as a Lead Auditor under MDR and/or IVDR.
Strong background in QMS auditing, technical file assessment, and applicable standards (ISO *****, ISO *****, etc.).
Skills:Deep technical knowledge of non-clinical aspects of medical device conformity assessment.
Proven ability to develop and deliver effective training.
Strong understanding of EU regulatory frameworks and best practice guidance.
Excellent stakeholder engagement, problem-solving, and communication skills.
Why SGS?
Opportunity to work with a global leader in inspection, verification, testing, and certification.
Collaborative and inclusive work environment.
Competitive salary and benefits package.
Opportunities for professional growth and development.
Join Us: At SGS, we are dedicated to fostering an open, friendly, and supportive culture that thrives on teamwork.
We value diversity and provide endless opportunities to learn, grow your expertise, and fulfil your potential.
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