QA Med Device Software job in Basel, Switzerland

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: Switzerland

This vacancy has now expired. Please see similar roles below...

We are in search of a Quality Expert Medical Device Software to support, review and maintenance of assigned processes of the Quality Management System and will as well support the development and commercialisation of assigned Medical Device Software Projects. This is a 12 month contract opportunity in Switzerland with the possibility of an extension.

Job Responsibilities

Provide QA functional expertise in the review of QMS processes for compliance to regulations, standards and guidelines related to Medical Device Software.
Manage portfolio of assigned projects, support a discipline and/or provide a service on his/her own or with a team of associates. Provide functional expertise in area of responsibility for medical device software.
Ensure that new medical device software products including web-based and mobile applications are developed, commercialised and maintained through its lifetime in compliance with medical device, software and data security regulations and standards.
Write, review and approve deliverables (e.g. procedures, records, device documentation) and related tools (e.g. IT, document systems, training tools) to ensure compliance to medical device and software regulations and standards.
Improve the overall quality of medical device software, tools and procedures, including peer reviews.
Manage quality problems and technical matters and ensure they are resolved consistently and in accordance with global standards and policies.
Represent MD Quality in initiatives and cross-divisional projects.
Support inspections and audits as required.
Support a culture of high performance and trust. Assure that the required level of knowledge and skills is available and identify competency gaps. Establish and implement training and development plans.
Meet internal and external guidelines regarding quality, safety and security (quality manuals, regulatory cGMP guidelines, health authority requirements, international standards, SOPs, HSE, etc.). Promote and enforce compliance to guidelines.
Support project management functions as a sub-team member in preparation for Inspection.
Write/contribute to internal compliance policy and/or comment to regulations.

Skills and Requirements

Graduate in a scientific field. Medical device software background.
Languages: English fluent in speaking / writing, German and/or French
At least 3 years of relevant experience.
Practical experience in managing projects in compliance with ISO 13485
Ability to influence people, negotiate and communicate.
Sound scientific, technical and regulatory knowledge in a specific area.
Excellent knowledge of cGMP, working knowledge of medical device software regulations, standards and guidelines.
Good knowledge of medical device software development and life-cycle management.
Good organisational skills. 8. Good and proven ability to analyse and evaluate GMP compliance.
Ability to work in cross-functional teams including Quality, Tec

To Apply

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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