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Quality Systems Specialist(m/w/x)
Subject matter expertise for quality systems in global healthcare technology. 4+ years medical device/pharma industry experience, Engineering degree, and French/English fluency essential. Flexible work arrangement, global improvement initiatives.
Requirements
- Minimum 4 years of relevant experience in medical device or pharmaceutical industry
- Minimum 2 years of quality experience
- Engineering bachelor's degree minimum
- Change control experience
- Fluency in French and English
- Excellent communication skills
- Ability to work in a team environment and independently
- Continuous improvement mindset
- High degree of initiative and good judgment
Tasks
- Ensure product quality and compliance
- Serve as the subject matter expert for quality systems
- Lead local improvement initiatives
- Develop a professional network and share best practices
- Contribute to global continuous improvement initiatives
- Oversee the development and maintenance of quality programs
- Monitor processes and report on key performance indicators
- Present and defend processes during audits and inspections
- Collaborate with manufacturing, engineering, and development teams
- Train stakeholders on quality processes
- Ensure compliance with ISO 13485, 21 CFR Part 820, and EU MDR
Work Experience
- 4 years
Education
- Compulsory education
Languages
- French – Business Fluent
- English – Business Fluent
Benefits
Flexible Working
- Flexible work arrangement
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Quality Systems Specialist(m/w/x)
Subject matter expertise for quality systems in global healthcare technology. 4+ years medical device/pharma industry experience, Engineering degree, and French/English fluency essential. Flexible work arrangement, global improvement initiatives.
Requirements
- Minimum 4 years of relevant experience in medical device or pharmaceutical industry
- Minimum 2 years of quality experience
- Engineering bachelor's degree minimum
- Change control experience
- Fluency in French and English
- Excellent communication skills
- Ability to work in a team environment and independently
- Continuous improvement mindset
- High degree of initiative and good judgment
Tasks
- Ensure product quality and compliance
- Serve as the subject matter expert for quality systems
- Lead local improvement initiatives
- Develop a professional network and share best practices
- Contribute to global continuous improvement initiatives
- Oversee the development and maintenance of quality programs
- Monitor processes and report on key performance indicators
- Present and defend processes during audits and inspections
- Collaborate with manufacturing, engineering, and development teams
- Train stakeholders on quality processes
- Ensure compliance with ISO 13485, 21 CFR Part 820, and EU MDR
Work Experience
- 4 years
Education
- Compulsory education
Languages
- French – Business Fluent
- English – Business Fluent
Benefits
Flexible Working
- Flexible work arrangement
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
SMO Medtronic Europe Sàrl
Industry
Healthcare
Description
The company leads global healthcare technology and addresses challenging health problems by finding solutions.
Not a perfect match?
- SMO Medtronic Europe Sàrl
Quality Systems Specialist(m/w/x)
Full-timeOn-siteExperiencedTolochenaz, Lausannefrom CHF 144,000 / year - SHQ Medtronic Int. Trading Sàrl
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Regulatory Affairs Specialist(m/w/x)
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Full-timeOn-siteExperiencedTolochenazfrom CHF 92,000 - 138,000 / year - SUSONITY
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