MDSAP Technical Pack Reviewer

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.

Main Purpose of Role

• To conduct reviews of MDSAP reports and approve or raise queries based on technical and procedural knowledge.
• Ensure that reviews are technically sound and in compliance with all applicable regulations, standards, guidelines and Competent Authority expectations.
• Ensure that the highest level of service is provided through efficient service delivery and that customer requirements are met.
• Ensure adherence to SGS Policies, procedures and processes.
• As a member of the Global Medical Device office (MDO) to minimise risks associated with medical device certification.

Key Accountabilities

• Maintain up-to-date understanding of MDSAP requirement, including all jurisdiction requirements, regulatory transmittals, MDSAP Audit Approach manual, and all associated standards.
• Maintain up-to-date understanding of the MDSAP grading system, corrective and preventive action, and use of the NGE form.
• Review MDSAP audit packs according to specified requirements.
• Generate Query Sheets for any noted deficiencies in the MDSAP audit pack.
• Review and accept/reject query corrections.
• Submit final approved documents to the Global MDSAP administrator for submission to REPS.
• Submit final approved document to the SGS system and approve the MDSAP pack.
• Approve MDSAP certificates after technical approval.
• Participate in team meetings.
• Maintain on-time reviews based on Regulatory requirements.
• Participate in achievement of KPIs.
• Determine final approval for MDSAP audit packages and the issue of MDSAP certificates.
• Signature authority for final MDSAP reports and NGE.
• If approved as an AO submitter, make submissions to REPS as required.
• Ensure full compliance with the Company’s Code of Integrity & Professional Conduct, and act in accordance with SGS UK’s Equality & Diversity Policy and ensure others do so.
• At all times, adopt a safe behaviour by exercising due regard for the health and safety of yourself, colleagues and clients, in line with the Company’s policies and procedures.

Skills & Knowledge

Essential

• Medical device knowledge/codes.
• Good communication techniques through electronic mediums.
• Good written English skills (as reports will be reviewed/queried in English).
• Thorough understand of risk management systems and requirements.
• Customer Focus.
• Teamwork.

Desirable

• Experience of working to KPI’s.
• Experience of planning own workload/priorities.
• Ability to work with online systems.

Experience

Essential

• Four years professional experience in the field of Medical Devices or related activities (Advanced degrees can substitute for a maximum of three years of working experience).
• In exceptional cases, a demonstration of equivalent knowledge and skills may be acceptable.
• Previous MDSAP Lead Auditor Experience.

Desirable

• Experience as Medical Device audit Technical Reviewer.
• Previous experience working for regulatory jurisdictions or with regulatory requirements of any MDSAP Member country.

Qualifications

Essential

• Successful completion of a university or technical college degree or equivalent qualification in relevant studies e.g. medicine, science, pharmacy, engineering or other relevant sciences.
• MDSAP Lead Auditor Qualification.

Desirable

• Advanced degrees in engineering, science, or other relevant areas.

Why SGS?

• Join a globally recognized and stable company, a leader in the Testing, Inspection, and Certification (TIC) industry.
• Enjoy a flexible schedule and work model.
• Access SGS University and Campus for continuous learning options.
• Thrive in a multinational environment, collaborating with colleagues from multiple continents.
• Benefit from our comprehensive benefits platform.

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 fulfill your potential.