Technical Manager QMS
Technical Manager QMS
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Salary Not Disclosed
1 Vacancy
Job Description
We are seeking a knowledgeable and driven Technical Manager QMS 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 1639.
Your Mission
As Technical Team Manager you will:
- 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 1639 activities and contribute to business development
Qualifications :
- Education: Bachelors 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 13485 ISO 14971 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
Additional Information :
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.
Remote Work :
Yes
Employment Type :
Full-time
Employment Type
Remote
Company Industry
Key Skills
- Mainframe
- ABAP
- Information Technology Sales
- Investment Management
- IT Service Desk
- Clinical
