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 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.

At SGS, we have an open corporate and international culture. We offer a dynamic work environment in a leading global company. Our high professional standards and our sustainability approach guarantee you a future-oriented work environment. We invest in our employees for the long term and are committed to supporting your development within the company. Our business principles include: Integrity, Health, Safety & Environment, Quality & Professionalism, Respect, Sustainability, and Leadership.

Job Description

As an In-house Clinician, you are a key member of the clinical team within Notified body. You work together with a group of clinicians and specialized product reviewers for the conformity assessment process of medical device. With your clinical expertise, you will provide clinical oversight to ensure that our clinical evaluation assessment of Medical Devices complies with EU MDR regulations.

This role is fully remote and we are only open to candidates with a valid work permit for the country of their residence.

More Specifically, You Will

Act as the primary clinical expertise within SGS Medical Device certification activities.
Review and scientifically challenge the clinical data contained within the clinical evaluation, and any associated clinical investigations.
Act as coordinator and guide external clinical expert in the clinical assessment and evaluate the results.
Be able to draw records and reports regarding clinical assessment, and make recommendation to Notified Body’s decision maker.
Develop, update and maintain appropriate training packages (with a focus of clinical evaluation assessments) for clinical experts and clinical specialists.
Offer appropriate clinical input into client queries and meetings.
Act as a final reviewer with regards to clinical aspects according to EU MDR regulation.

Qualifications

Essential:

A qualified Dentist with minimum two years of working experience is a must have.
University degree (Dentistry) plus further academic training in a clinically research and/or medical device related area.
Fluent in English, reading and writing.

Desirable

Knowledge of the Medical Device Regulation (MDR) and relevant guidance documents (e.g., MDCG, MEDDEV).
At least two years experience in the assessment of clinical data for medical devices in a Notified Body would be a strong advantage.
Experience working with a Notified Body and/or experience writing or assessing Clinical Evaluation Reports (CERs).

Additional Information

We provide remote working environment.
Opportunity to work with a global leader in inspection, verification, testing, and certification.
Collaborative and inclusive work environment.
Working Hours: This role is a part‑time position at 40% FTE (approximately 2 days per week).
Opportunities for professional growth and development.

Please send your CV in English.

SGS

New Jobs

In house Clinician – Dental (Part time, %40 FTE)