Description
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Job Function:
QualityJob Sub Function:
Customer/Commercial QualityJob Category:
ProfessionalAll Job Posting Locations:
Zuchwil, SwitzerlandJob 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, as may be required, 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.
Job Overview
The CQ Specialist Supplier Management is responsible for leading Commercial Quality activities related to supplier oversight to ensure compliance, product quality, and supply continuity. This role provides hands-on supervision and subject matter leadership across supplier quality processes, including qualification, performance monitoring, and issue resolution. The position plays a key role in strengthening supplier partnerships, mitigating risk, and supporting uninterrupted delivery of high-quality medical devices to customers and patients.
Key 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:
Required:
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 workstreams.
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 www.careers.jnj.com.
Required Skills:
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