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Quality Supervisor(m/w/x)
Description
In this role, you will be at the forefront of quality assurance, collaborating with teams to uphold product standards, managing a dedicated quality engineering team, and driving continuous improvement initiatives to enhance processes and compliance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor's degree
- •5-6 years of related experience
- •Previous supervisory experience
- •Experience in Medical Device, Pharmaceuticals, or Mechanical field
- •Fluency in English and German
Education
Work Experience
5 - 6 years
Tasks
- •Collaborate with production and engineering teams to ensure product quality
- •Manage daily tasks of quality engineers supporting production
- •Prepare and revise quality control documents
- •Recommend quality control tools and methods
- •Assess nonconforming products
- •Support resolution of quality issues
- •Oversee the nonconformity process and participate in investigations
- •Recommend product dispositions and advise on corrective actions
- •Prepare, maintain, and analyze quality KPIs
- •Lead internal and external meetings to report on NC, CAPA, and improvement efforts
- •Drive product and process improvement using CAPA and Kaizen methodologies
- •Provide production and quality data for regulatory authority requests
- •Act as a subject matter expert for audits
- •Recruit, interview, and hire quality engineering team members
- •Train and develop team members
- •Define objectives and monitor team performance
Languages
English – Business Fluent
German – Business Fluent
Benefits
Bonuses & Incentives
- •Bonussystem
More Vacation Days
- •Extra Urlaubstage
- StrykerFull-timeOn-siteSeniorSelzach
- Stryker
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Quality Supervisor(m/w/x)
The AI Job Search Engine
Description
In this role, you will be at the forefront of quality assurance, collaborating with teams to uphold product standards, managing a dedicated quality engineering team, and driving continuous improvement initiatives to enhance processes and compliance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor's degree
- •5-6 years of related experience
- •Previous supervisory experience
- •Experience in Medical Device, Pharmaceuticals, or Mechanical field
- •Fluency in English and German
Education
Work Experience
5 - 6 years
Tasks
- •Collaborate with production and engineering teams to ensure product quality
- •Manage daily tasks of quality engineers supporting production
- •Prepare and revise quality control documents
- •Recommend quality control tools and methods
- •Assess nonconforming products
- •Support resolution of quality issues
- •Oversee the nonconformity process and participate in investigations
- •Recommend product dispositions and advise on corrective actions
- •Prepare, maintain, and analyze quality KPIs
- •Lead internal and external meetings to report on NC, CAPA, and improvement efforts
- •Drive product and process improvement using CAPA and Kaizen methodologies
- •Provide production and quality data for regulatory authority requests
- •Act as a subject matter expert for audits
- •Recruit, interview, and hire quality engineering team members
- •Train and develop team members
- •Define objectives and monitor team performance
Languages
English – Business Fluent
German – Business Fluent
Benefits
Bonuses & Incentives
- •Bonussystem
More Vacation Days
- •Extra Urlaubstage
About the Company
Jabil Switzerland Manufacturing GmbH
Industry
Healthcare
Description
Das Unternehmen ist der weltweit größte Hersteller von Healthcare-Design und Herstellungsdienstleistungen und verbessert die Gesundheit der Menschen.
- Stryker
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Junior Process Engineer(m/w/x)
Full-timeOn-siteJuniorBettlach - Jabil Switzerland Manufacturing GmbH
Group Leader(m/w/x)
Full-timeOn-siteSeniorGrenchen - Adragos Pharma - BACCINEX SA
Quality & Regulatory Dossier Compliance Specialist(m/w/x)
Full-timeOn-siteManagementCourroux