Assoc. Director, Quality Management, Manufacturing
Listed on 2026-01-01
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Engineering
Regulatory Compliance Specialist, Quality Engineering
Location: Eysins
Assoc. Director, Quality Management, Contract Manufacturing
Reports to: Vice President of Quality EMI Function.
Location: Canton of Vaud, Switzerland. Candidates must hold a valid Swiss work visa or have existing work authorization.
Overview: We are seeking an Associate Director of Quality Management to join our International Infusion Leadership team, bringing ~10 years of senior experience in regulated industries such as Med Tech, pharmaceuticals, aerospace, and automotive. In this role, you will lead quality assurance for Electromechanical Instrumentation (EMI) contract manufacturing, leveraging deep expertise in QMS, product design, manufacturing, and supply chain to drive compliance, performance, and continuous improvement across global supplier networks.
With extensive knowledge of medical device regulations, you will influence strategy, strengthen governance, and ensure regulatory excellence.
- Lead and develop a dedicated Contract Manufacturing Quality team.
- Drive supplier qualification, audits, and performance management.
- Champion continuous improvement using Lean, Six Sigma, and advanced quality methodologies.
- Partner with design, manufacturing, supply chain, and procurement leaders to resolve challenges and enhance supplier capabilities.
- Represent the organization during FDA and notified body inspections.
- Report key metrics and trends to senior leadership, shaping long‑term strategy.
- Bachelor’s degree in a technical field (Engineering preferred);
Master’s degree a plus. - 10+ years of experience in electromechanical instrumentation manufacturing, quality assurance, and regulatory compliance in regulated industries (Med Tech, pharma, aerospace, automotive).
- Strong QMS expertise; product design, manufacturing, supply chain knowledge; ideally electromechanical.
- Deep knowledge of ISO 13485, FDA QSR (21 CFR Part 820), ISO 14971, and international medical device regulations.
- Strong leadership, project management, and cross‑regional coordination skills.
- Ability to influence stakeholders and drive results in complex environments.
Compensation range: 180 kCHF to 200 kCHF
Why this role?This is more than a quality leadership role — it’s a chance to make a tangible impact on patient safety and product excellence worldwide. You’ll be part of a collaborative leadership team, with the resources and support to innovate, grow, and shape the future of medical device manufacturing.
Equality and InclusionBecton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, citizenship status, marital or domestic union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
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