PpDePuy Synthes is recruiting for a CQ Specialist Core QMS located in Zuchwil, Solothurn, Switzerland. /p h3Key Responsibilities /h3 ul liSupport the maintenance, implementation, and continuous improvement of the Core Quality Management System (QMS). /li liAuthor, review, and update global quality procedures, work instructions, and related documentation. /li liEnsure QMS processes align with applicable regulatory requirements (e.g., ISO 13485, FDA QSR, MDR) and internal standards. /li liSupport internal, external, and regulatory audits, including preparation, execution, and follow‑up of corrective actions. /li liTrack, analyze, and report QMS metrics and performance indicators to support data‑driven decision‑making. /li liCollaborate with cross‑functional stakeholders to assess process changes and support change management activities. /li liSupport CAPA, deviation, and continuous improvement initiatives related to QMS processes. /li liContribute to training activities to ensure effective understanding and adoption of QMS requirements. /li /ul h3Qualifications /h3 ul liBachelor’s degree in Life Sciences, Engineering, Quality, or a related discipline (required). /li liAdvanced degree or formal training in Quality or Regulatory Affairs (preferred). /li liApproximately 3–5 years of relevant experience in Quality, Compliance, or Regulatory Affairs within a regulated industry, preferably medical devices. /li liWorking knowledge of Quality Management Systems and global quality standards. /li liExperience supporting audits and inspection readiness activities. /li liAbility to analyze quality data and support continuous improvement initiatives. /li /ul h3Preferred /h3 ul liExperience working in a global or matrixed organization. /li liFamiliarity with digital QMS tools and document management systems. /li liKnowledge of EU MDR and other international regulatory frameworks. /li liExperience supporting process harmonization or global quality initiatives. /li liLean, Six Sigma, or continuous improvement exposure. /li liStrong documentation, technical writing, and organizational skills. /li liEffective communication skills and ability to collaborate across functions. /li /ul h3Other /h3 ul liLanguages: Fluency in English required; German preferred. /li liTravel: Limited; Up to 10%, primarily international. /li liCertifications: ASQ or equivalent Quality certification preferred. /li /ul pJohnson 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. /p /p #J-18808-Ljbffr