Medical Device Technical Pack Reviewer / Certification Decision Maker

SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.

At SGS Belgium NV, Certification and Business Enhancement we have an excellent opportunity for a Medical Device Technical Pack Reviewer to join the Belgian NoBo Medical Devices team

The successful candidate will be responsible to undertake technical reviews and certification decisions of audit packs within target timescales and in line with SGS policies and accreditation/approval requirements

Job description:

  • To undertake technical reviews and certification decisions of audit packs within target timescales and in line with SGS policies and accreditation/approval requirements

  • Provide accurate and timely reporting as required by line management to assist the planning and management of operations

  • Undertake personal professional development and ensure appropriate training records and personal logs are updated to maintain relevant auditor registrations and relevant industry knowledge

  • To maintain a full knowledge and understanding of SGS procedures and external approval criteria to allow efficient and effective technical reviews.

  • To undertake other technical tasks as requested  and support affiliates on technical projects

  • Maintain medical device auditor status whilst not undertaking significant number of audits

Profile

  • Must be able to demonstrate and excellent working knowledge of medical device management and regulatory systems [MDD, IVDD, Accreditation], standards and compliance/auditing techniques (Essential)

  • Effective interpersonal skills; able to develop good working relationships with people at all levels (Essential)

  • Must be IT literate i.e. competent in the use of MS Office applications (Essential)

  • Willingness to learn and adapt to change – committed to continuous personal and professional development (Essential)

  • Minimum of 2 years working for a Medical Device Notified Body

  • Minimum of 5 years medical device experience from auditing/work ( Essential)

  • Minimum 3 year experience auditing against recognised standards (Essential)

  • Approval as a Notified Body  Product Assessor (not required to be active but must have had in past with NB)

  • MDD, IVDD,  CMDCAS auditor approval or part off (not required to be active but must have had in past with NB)

  • Experience of working under own initiative and in planning and prioritising workloads (Essential)

  • Experience of reviewing audit packs (Desirable)

  • Registered IRCA lead auditor, or equivalent registration under other recognised body (Desirable)

  • University Degree or equivalent

If you are interested in this position, please apply with your resume and motivation letter to pascal [dot] plessers [at] sgs [dot] com

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