CQ Specialist Core QMS
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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) CQ Specialist Core QMS, located in Zuchwil, Solothurn, Switzerland.
The CQ Specialist Core QMS supports the effectiveness, compliance, and continuous improvement of the DePuy Synthes Quality Management System (QMS). This role partners closely with Quality, Regulatory Affairs, and cross‑functional teams to ensure global processes meet internal standards and applicable regulatory requirements. The position plays a key role in maintaining audit readiness, strengthening process consistency, and enabling a culture of quality and compliance across DPS.
Key Responsibilities
Support the maintenance, implementation, and continuous improvement of the Core Quality Management System (QMS).
Author, review, and update global quality procedures, work instructions, and related documentation.
Ensure QMS processes align with applicable regulatory requirements (e.g., ISO 13485, FDA QSR, MDR) and internal standards.
Support internal, external, and regulatory audits, including preparation, execution, and follow‑up of corrective actions.
Track, analyze, and report QMS metrics and performance indicators to support data‑driven decision‑making.
Collaborate with cross‑functional stakeholders to assess process changes and support change management activities.
Support CAPA, deviation, and continuous improvement initiatives related to QMS processes.
Contribute to training activities to ensure effective understanding and adoption of QMS requirements.
Qualifications
Education
Required: Bachelor’s degree in Life Sciences, Engineering, Quality, or a related discipline
Preferred: Advanced degree or formal training in Quality or Regulatory Affairs
Experience and Skills
Required:
Approximately 3–5 years of relevant experience in Quality, Compliance, or Regulatory Affairs within a regulated industry, preferably medical devices
Working knowledge of Quality Management Systems and global quality standards
Experience supporting audits and inspection readiness activities
Ability to analyze quality data and support continuous improvement initiatives
Preferred:
Experience working in a global or matrixed organization
Familiarity with digital QMS tools and document management systems
Knowledge of EU MDR and other international regulatory frameworks
Experience supporting process harmonization or global quality initiatives
Lean, Six Sigma, or continuous improvement exposure
Strong documentation, technical writing, and organizational skills
Effective communication skills and ability to collaborate across functions
Other
Languages: Fluency in English required; German preferred
Travel: Limited; Up to 10%, primarily international
Certifications: ASQ or equivalent Quality certification 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.
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics 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.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
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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 EnvironmentYou'll be redirected to
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