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11514en
- Contract
- English
- Associate
- Engineering & Technical Services
- Aarau, Basel
- Healthcare & Life Sciences
Skills
Quality Assurance, Manufacturing, GMP, Design Control
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This vacancy has now expired
On behalf of our clients, two International leader in Healthcare & Lifesciences, Swisslinx is looking for a Quality Engineer. This is a great opportunity to bring your proven knowledge and expertise to an organization that offers a dynamic working environment. These are contract position for at least 6 months with the possibility of extension.
Your mission:
- Support the assigned combination product development project(s) from the Design Quality perspective. Ensure that all design development work meets applicable FDA and EU MDR requirements
- Author SOPs and Guidelines for the medical device and combination product department and harmonize design control & risk management documentation
- Collaborate with the suppliers / CMOs on the following topics: qualification audits; vendor performance issues, deviations and SCARs; review and approval of drawings, specs and test reports; Quality Agreements; process validation, equipment qualification, etc.
- Provide regular progress reports and escalate potential risks related to Quality System and/or project status to Quality management and stakeholders
Your background
- Minimum Bachelor’s degree in chemical, mechanical or bio-engineering
- At least 5 years of experience in related quality engineering field
- Broad and deep understanding of disciplined quality product development processes,
regulatory, and quality / risk management systems (ISO 13485, MDR, 21CFR820, ISO14971…)
- Highly analytical and a functional team-player
- Fluent in English and ideally German
Candidates must have a valid Swiss or European permit or work rights to be considered for this position. If you would like to be considered for the role, please apply directly or send your CV to fiona.maqi@swisslinx.com.
Your mission:
- Support the assigned combination product development project(s) from the Design Quality perspective. Ensure that all design development work meets applicable FDA and EU MDR requirements
- Author SOPs and Guidelines for the medical device and combination product department and harmonize design control & risk management documentation
- Collaborate with the suppliers / CMOs on the following topics: qualification audits; vendor performance issues, deviations and SCARs; review and approval of drawings, specs and test reports; Quality Agreements; process validation, equipment qualification, etc.
- Provide regular progress reports and escalate potential risks related to Quality System and/or project status to Quality management and stakeholders
Your background
- Minimum Bachelor’s degree in chemical, mechanical or bio-engineering
- At least 5 years of experience in related quality engineering field
- Broad and deep understanding of disciplined quality product development processes,
regulatory, and quality / risk management systems (ISO 13485, MDR, 21CFR820, ISO14971…)
- Highly analytical and a functional team-player
- Fluent in English and ideally German
Candidates must have a valid Swiss or European permit or work rights to be considered for this position. If you would like to be considered for the role, please apply directly or send your CV to fiona.maqi@swisslinx.com.
