Auditor Independent Reviewer to Intertek Medical Notified Body

Antal platser:
Yrkesbenämning: Revisor
Publicerad: 2023-01-17
Sista ansökningsdag: 2023-02-17
Stad: Stockholm
Be a part of our journey to make the work safer! We are looking for an Auditor Independent Reviewer for a home-based role in either Sweden or the UK. About Intertek Intertek is the trusted service provider to many of the world’s leading brands, companies, and governments, and has earned a reputation for accuracy, reliability, integrity, and technical competence. Our Assurance, Testing, Inspection, and Certification services take us into nearly every field, from textiles, toys, and electronics, to building, heating, pharmaceuticals, petroleum, food, cargo scanning, and medical devices. In a world where a company’s success depends on its reputation for quality, safety, and socially responsible products and processes, Intertek employees make a difference. About the role As an auditor independent reviewer at Intertek, you will perform technical reviews of audit reports of our client’s quality management systems in accordance with regulatory requirements. You will also participate in disputes and appeals received from clients and with your technical input make decisions on whether to uphold or not and support the Certification Manager during Competent Authority audits and inspections. The role as auditor also includes: • Maintaining accurate and current training and assessment history records as part of ongoing competency evidence and development. • Achieving KPI objectives for the certification processes • Comply with Intertek’s Quality Management System • Ensuring confidentiality and independence from commercial and other interests, and raising any existing or prior association with clients to line manager immediately This position is a home-based role in either UK or Sweden. Who are you? You have 3+ years of experience as a Lead Auditor or decision maker at a Medical Notified Body and preferably experience of either working in a health science related industry in clinical affairs, design, manufacturing or quality and regulatory functions, or previous experience with testing laboratories. As a person you are keen to details and take pride in delivering accurate and robust assessments within agreed time frames. You also have • an appropriate degree or other qualifications and/or experience in either health science, engineering or quality/regulatory disciplines related to the medical device or pharma industry sectors • current Lead Auditor qualification • good knowledge the EU Medical Device Directives and EU and UK Medical Device Regulations, and (EN) ISO 13485 Quality Management Systems What we offer Intertek is a safe workplace with collective agreements, benefit package with pension, health care contributions and parental leave allowance. We have flexible working hours and encourage a good working climate and satisfied employees. Submit your application with resume and cover letter today, or as soon as possible. We have no possibility to handle applications through email so please submit your CV through the application link. If you have any questions regarding the position, don’t hesitate to contact our recruiter Alexandra Strand Hägglund, [email protected]

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