Jabil
QualityEngineer
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Engineer at Jabil. Skills: Quality Engineering, Quality Control, CAPA, ISO 13485, 21CFR820. Be part of the quality team in Jabil Bettlach factory. Collaborate with production and engineering teams to ensure products meet quality and regulatory requirements”
What You'll Achieve.
ensure products meet quality and regulatory requirements; effectiveness monitoring
Industry & Context.
problem‑solving; quality issues resolution; investigations; improvements; remediation actions
comply with safety and security requirements
What They're Looking For.
Must Have
Experience in manufacturing, quality or engineering required, Experience in ISO 13485 and 21CFR820 medical device regulated industry, Fluent in English and German
Nice to Have
Experience in CNC and surface treatment is a plus, Experience in production and quality system MES, SAP, ETQ, Babtec is a plus
What You'll Do.
Be part of the quality team in Jabil Bettlach factory
Collaborate with production and engineering teams to ensure products meet quality and regulatory requirements
Create quality control documents
and provide recommendation on quality control tools and methods
Prepare First Article Inspection instructions
Assess nonconforming products
recommend product disposition and support in quality issues resolution etc.
Participate in nonconformities and CAPA: investigations
effectiveness monitoring
Lead product and process improvement quality efforts through CAPA and Kaizen methodology
Act as SME for projects e. g. new equipment or new products introduction
product/process improvements
Support internal and external audits preparation with Gemba walks and remediation actions
Support in risk assessment of manufacturing process
How You'll Work.
Team & Collaboration
Collaborate with production and engineering teams; Ability to work cross‑functionally and communicate effectively across teams
Communication Scope
communicate effectively across teams
Process & Methodology
Lead product and process improvement quality efforts, Act as SME for projects e. g. new equipment or new products introduction, product/process improvements
Full Job Description
At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe. We are looking for a new team member in the role as # **Quality Engineer (m/f/d)- 100%** **Location** : Bettlach (SO), Switzerland **Type of Contract** : permanent employment **Startdate:** ASAP **Shift work** : No ## **YOUR RESPONSIBILITIES** * Be part of the quality team in Jabil Bettlach factory. Collaborate with production and engineering teams to ensure products meet quality and regulatory requirements. * Create quality control documents, and provide recommendation on quality control tools and methods. * Prepare First Article Inspection instructions * Assess nonconforming products, recommend product disposition and support in quality issues resolution etc. * Participate in nonconformities and CAPA: investigations, product disposition, improvements, effectiveness monitoring. * Lead product and process improvement quality efforts through CAPA and Kaizen methodology. * Act as SME for projects e.g. new equipment or new products introduction, product/process improvements. * Support internal and external audits preparation with Gemba walks and remediation actions. * Support in risk assessment of manufacturing process. ## **YOUR BACKGROUND** * Bachelor’s degree preferred, or an equivalent combination of education and relevant experience * Experience in manufacturing, quality or engineering required * Experience in ISO 13485 and 21CFR820 medical device regulated industry * Experience in CNC and surface treatment is a plus * Experien
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