Jabil Switzerland Manufacturing GmbH
Quality Supervisor(m/w/x)
Full-timeOn-siteSenior
Bettlach
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Establishing a center of excellence for product consistency and safety investigations on Trauma & Extremities implants at a global medtech manufacturer. In-depth knowledge of ISO, FDA, and international regulatory requirements required. Global collaboration on product safety and consistency.
Requirements
- Knowledge of regulatory requirements, including ISO, FDA, and International requirements
- Technical knowledge of medical device product lines
- Written, verbal, listening, communication, and team-building skills
- Ability to collaborate effectively and lead cross-functional teams
- Ability to prioritize and manage multiple project workloads
- Experience with trending and analysis reporting
- Knowledge of adverse event reporting, complaint investigation, CAPA, and corrective action processes
- Leadership skills
- Process improvement and management skills
- Experience with recruiting and people development
- Influence across the organization
- Entrepreneurial spirit for driving business forward
- Accountability for collaborating with global colleagues
- Predisposition for coaching and mentoring
- Strong emotional intelligence
- Exceptional communication skills to influence decision makers
- Great interpersonal skills and teamwork
- Strong leadership skills for team engagement
- Service-minded and courageous
- BS in a science, engineering or related field; advanced degree preferred
- Minimum of 10 years experience, 7 years of supervisory experience preferred
- Masters Degree or equivalent preferred
- Experience working in a regulated environment
- Good understanding of manufacturing process technologies
- Experience with delivering results through 6 sigma and lean methods
- Strong analytical ability and relevant ERP knowledge (preferably SAP, Oracle or JDEdwards)
Tasks
- Establish a quality center of excellence
- Develop organizational strategies and processes
- Set goals and metrics for quality improvements
- Oversee consistency of quality processes
- Manage product and safety investigations
- Evaluate day-to-day quality processes
- Establish annual budgets and quarterly forecasts
- Collaborate with various departments to meet corporate goals
- Develop teams for timely resolution of technical issues
- Serve as a site leader for GQO quality processes
- Provide guidance on regulatory requirements
- Establish processes for task resolution management
- Chair meetings to drive closure of quality issues
- Manage and update quality metrics
- Represent quality processes during audits
- Define targets and KPIs for team members
- Recruit and onboard top talent
- Develop team talent to enhance performance
- Maintain high team engagement levels
Work Experience
- 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAP
- Oracle
- JDEdwards
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Stryker and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- Stryker
Spezialist Qualitätskontrolle(m/w/x)
Full-timeOn-siteSeniorSelzach - Jabil Switzerland Manufacturing GmbH
Process Engineer(m/w/x)
Full-timeOn-siteExperiencedGrenchen - Jabil Switzerland Manufacturing GmbH
Group Leader(m/w/x)
Full-timeOn-siteSeniorGrenchen - Jabil Switzerland Manufacturing GmbH
Junior Process Engineer(m/w/x)
Full-timeOn-siteJuniorBettlach
Establishing a center of excellence for product consistency and safety investigations on Trauma & Extremities implants at a global medtech manufacturer. In-depth knowledge of ISO, FDA, and international regulatory requirements required. Global collaboration on product safety and consistency.
Requirements
- Knowledge of regulatory requirements, including ISO, FDA, and International requirements
- Technical knowledge of medical device product lines
- Written, verbal, listening, communication, and team-building skills
- Ability to collaborate effectively and lead cross-functional teams
- Ability to prioritize and manage multiple project workloads
- Experience with trending and analysis reporting
- Knowledge of adverse event reporting, complaint investigation, CAPA, and corrective action processes
- Leadership skills
- Process improvement and management skills
- Experience with recruiting and people development
- Influence across the organization
- Entrepreneurial spirit for driving business forward
- Accountability for collaborating with global colleagues
- Predisposition for coaching and mentoring
- Strong emotional intelligence
- Exceptional communication skills to influence decision makers
- Great interpersonal skills and teamwork
- Strong leadership skills for team engagement
- Service-minded and courageous
- BS in a science, engineering or related field; advanced degree preferred
- Minimum of 10 years experience, 7 years of supervisory experience preferred
- Masters Degree or equivalent preferred
- Experience working in a regulated environment
- Good understanding of manufacturing process technologies
- Experience with delivering results through 6 sigma and lean methods
- Strong analytical ability and relevant ERP knowledge (preferably SAP, Oracle or JDEdwards)
Tasks
- Establish a quality center of excellence
- Develop organizational strategies and processes
- Set goals and metrics for quality improvements
- Oversee consistency of quality processes
- Manage product and safety investigations
- Evaluate day-to-day quality processes
- Establish annual budgets and quarterly forecasts
- Collaborate with various departments to meet corporate goals
- Develop teams for timely resolution of technical issues
- Serve as a site leader for GQO quality processes
- Provide guidance on regulatory requirements
- Establish processes for task resolution management
- Chair meetings to drive closure of quality issues
- Manage and update quality metrics
- Represent quality processes during audits
- Define targets and KPIs for team members
- Recruit and onboard top talent
- Develop team talent to enhance performance
- Maintain high team engagement levels
Work Experience
- 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAP
- Oracle
- JDEdwards
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Stryker and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Stryker
Industry
Other
Description
Das Unternehmen ist ein globales Medizintechnikunternehmen, das hochwertige Implantate für den Bereich Trauma & Extremities fertigt.
Not a perfect match?
- Jabil Switzerland Manufacturing GmbH
Quality Supervisor(m/w/x)
Full-timeOn-siteSeniorBettlach - Stryker
Spezialist Qualitätskontrolle(m/w/x)
Full-timeOn-siteSeniorSelzach - Jabil Switzerland Manufacturing GmbH
Process Engineer(m/w/x)
Full-timeOn-siteExperiencedGrenchen - Jabil Switzerland Manufacturing GmbH
Group Leader(m/w/x)
Full-timeOn-siteSeniorGrenchen - Jabil Switzerland Manufacturing GmbH
Junior Process Engineer(m/w/x)
Full-timeOn-siteJuniorBettlach