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Quality Systems Specialist(m/w/x)
Description
As a Quality Systems Specialist, you will focus on ensuring the quality of life-saving products while leading improvement initiatives and collaborating with various teams. Your role involves training stakeholders, monitoring compliance, and preparing for audits, all of which make a significant impact on product quality and safety.
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Upload your CV and Nejo AI will find matching job offers for you.
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
Education
Work Experience
4 years
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
Languages
French – Business Fluent
English – Business Fluent
Benefits
Flexible Working
- •Flexible work arrangement
- SMO Medtronic Europe SàrlFull-timeOn-siteExperiencedfrom CHF 144,000 / yearTolochenaz, Lausanne
- SHQ Medtronic Int. Trading Sàrl
Regulatory Affairs Specialist(m/w/x)
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Regulatory Affairs Specialist(m/w/x)
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Internship QC support(m/w/x)
Full-timeInternshipOn-siteCorsier-sur-Vevey - SMO Medtronic Europe Sàrl
Intern Process Development Engineering(m/w/x)
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Quality Systems Specialist(m/w/x)
The AI Job Search Engine
Description
As a Quality Systems Specialist, you will focus on ensuring the quality of life-saving products while leading improvement initiatives and collaborating with various teams. Your role involves training stakeholders, monitoring compliance, and preparing for audits, all of which make a significant impact on product quality and safety.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
Work Experience
4 years
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
Languages
French – Business Fluent
English – Business Fluent
Benefits
Flexible Working
- •Flexible work arrangement
About the Company
SMO Medtronic Europe Sàrl
Industry
Healthcare
Description
The company leads global healthcare technology and addresses challenging health problems by finding solutions.
- SMO Medtronic Europe Sàrl
Quality Systems Specialist(m/w/x)
Full-timeOn-siteExperiencedfrom CHF 144,000 / yearTolochenaz, Lausanne - SHQ Medtronic Int. Trading Sàrl
Regulatory Affairs Specialist(m/w/x)
Full-timeOn-siteExperiencedLausanne - Medtronic
Regulatory Affairs Specialist(m/w/x)
Full-timeOn-siteExperiencedLausanne - SUSONITY
Internship QC support(m/w/x)
Full-timeInternshipOn-siteCorsier-sur-Vevey - SMO Medtronic Europe Sàrl
Intern Process Development Engineering(m/w/x)
Full-timeInternshipOn-sitefrom CHF 2,000 - 2,500 / monthLausanne