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CQ Specialist Supplier Mgmt

Job in 4528, Zuchwil, Kanton Solothurn, Switzerland
Listing for: Johnson & Johnson
Full Time position
Listed on 2026-06-30
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CHF Yearly CHF 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: Zuchwil

Overview

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we aim to deliver breakthroughs of tomorrow and profoundly impact health for humanity.

Learn more at

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered an individual. We respect the diversity and dignity of our employees and recognize their merit.

Job Details

Job Function: Quality

Job Sub Function: Customer/Commercial Quality

Job Category: Professional

All Job Posting Locations: Zuchwil, Switzerland

Job Description

DePuy Synthes is recruiting for a(n) Commercial Quality Specialist, Supplier Management, located in Zuchwil, Solothurn.

Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans.

In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

Responsibilities
  • Lead and oversee Commercial Quality supplier management activities, ensuring compliance with internal quality systems and applicable regulatory requirements.
  • Support supplier qualification, onboarding, and ongoing performance monitoring activities.
  • Manage supplier‑related quality events, including nonconformances, investigations, and corrective and preventive actions (CAPA).
  • Partner with Procurement, Manufacturing, Supply Chain, and Regulatory Affairs to address supplier quality issues and drive timely resolution.
  • Support supplier audits and assessments, including preparation, execution, and follow‑up actions.
  • Monitor supplier quality metrics and trends to identify risks and improvement opportunities.
  • Drive continuous improvement initiatives to enhance supplier quality performance and process robustness.
Qualifications

Education:

  • Bachelor’s degree required in Engineering, Life Sciences, Supply Chain, or a related scientific or technical discipline.
  • Advanced degree preferred.

Experience and Skills:

  • 4–6 years of experience in Quality Assurance, Commercial Quality, or supplier quality management within a regulated medical device or pharmaceutical environment.
  • Previous experience leading supplier focused quality activities or work streams.
  • Strong knowledge of quality management systems and supplier quality processes.
  • Experience managing supplier investigations, nonconformances, and CAPA.
  • Ability to work cross‑functionally and influence internal and external stakeholders.
  • Strong analytical, organizational, and problem‑solving skills.
Preferred
  • Experience supporting EU MDR‑regulated medical device products.
  • Experience conducting or supporting supplier audits and assessments.
  • Experience in orthopedic or implantable medical device products.
  • Familiarity with supplier performance metrics and risk‑based monitoring approaches.
  • Knowledge of continuous improvement or risk management methodologies.
Other
  • Language: Fluent in English;
    German preferred.
  • Travel: Moderate international travel.
  • Certifications: Quality‑related certifications (e.g., ISO, ASQ) preferred.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit

Skills: Required Skills and Preferred

Skills:

Audit Management, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment

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