Qms Lead Auditor Manager
5 meses atrás
Company Description
We are SGS - the world’s leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 98,000employees operate a network of 2,650 offices and laboratories, working together to enable a better, safer and more interconnected world.
**Job Description**:
NB1639, part of SGS Belgium NV, is one to the European Notified Bodies designated for MDR. Presently, our team is taking care of a global client base whom are either transferring their products to the new regulation or are bringing their innovative products to the European Market. Our team is comprised of highly competent and skilled staff each playing an important role in bringing safe and efficacious Medical devices to the patient.
**Key Accountabilities**:
- Support with competency approval
- To act as mentor for new Auditors when needed
- To help with update procedure and forms relevant to medical device QMS auditors to improve the efficiency and productivity
- To act as technical managers for all auditors globally and support them with daily queries (technical or operational).
- To provide training to Medical device auditors.
- To Conduct audits at clients in order to maintain competency
- Complete specific projects in relation to medical device procedures, processes, systems and documentation as requested by the Medical Devices Manager.
**Qualifications**:
Please submit your CV in English.
A minimum of 4 years ‘hands-on’ professional experience of designing, manufacturing or testing medical devices:
- A university degree or equivalent qualification in relevant sciences such as: Chemistry, Biochemistry, Biology, Microbiology, Biotechnology, Physics, Biophysics, Material Science Biomedical Engineering, Mechanical, Electrical or Electronic Engineering, Computer & Software Technology.
- Previous working experience as Lead Auditor against MDD or MDR within a notified body
Knowledge of:
- Medical devices (active, non-active or software) and Medical device management systems.
- EU MDD 93/42/EEC (UK MDR 2002), EU MDR 2017/745, EU IVDR 2017/746, ISO 13485.
- Medical Device Standards.
In addition:
- Experience of working under own initiative and in planning and prioritizing workloads.
- Full driving licence.
- Good English written and verbal skills.
The following attributes would be desirable, but not essential:
- Registered IRCA lead auditor, or equivalent registration under other recognized body.
- Experience in delivering training and in engaging and working with people in all levels of an organisation.
- Previous management experience
- Previous training and mentoring experience
Additional Information
**This position will be hybrid or fully remote depending on the location.
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