Johnson & Johnson AG
Manager, Source Reg Compliance (EMEA)
📍 Zug, Switzerland, 6300 Zug
Rolle und Verantwortlichkeiten
The Manager, Source Regulatory Compliance (EMEA) is responsible for leading regulatory compliance activities related to sourcing, suppliers, and externally provided processes across the EMEA region. This role ensures that suppliers, contract manufacturers, and sourced materials comply with applicable regulatory requirements, quality system standards, and internal policies. The position plays a critical role in safeguarding product quality, supporting audit readiness, and enabling compliant supply continuity by partnering closely with Quality, Regulatory Affairs, Supply Chain, and Procurement teams across multiple countries. Execute source regulatory compliance activities including supplier audit execution, investigation approval, and objective evidence review, to ensure adherence to regulatory and quality system requirements. Provide regulatory compliance oversight for suppliers, contract manufacturers, and externally provided processes. Partner with Supply Chain, Procurement, Quality, and Regulatory Affairs teams to support compliant supplier qualification, monitoring, and lifecycle management. Interpret global regulatory requirements and translate them into sourcing and supplier compliance expectations. Support internal audits, external audits, and health authority inspections related to sourcing and supplier compliance. Monitor compliance risks, trends, and supplier performance metrics; drive corrective and preventive actions. Ensure accurate maintenance of compliance documentation, records, and reports. Contributes to continuous improvement initiatives to strengthen supplier compliance governance and effectiveness.
Team / Beschreibung
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 MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. 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 as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Qualifikationen und Fähigkeiten
Bachelor’s degree in Engineering, Life Sciences, Supply Chain, or a related discipline (required).
Advanced degree in a scientific, regulatory, or business field (preferred).
Typically 6-8 years of progressive experience in Regulatory Compliance, Quality, Supply Chain, or related roles within a regulated industry.
Strong working knowledge of global regulatory and quality requirements impacting supplier operations.
Experience leading supplier audits, inspections, and compliance assessments.
Ability to manage complex compliance topics across multiple countries and stakeholder groups.
Experience in medical devices, healthcare, or other highly regulated industries (preferred).
Familiarity with global regulatory and supplier compliance frameworks (preferred).
Experience working in a global or matrixed organization (preferred).
Exposure to regulatory inspections involving supplier or contract manufacturing oversight (preferred).
Quality or Regulatory certifications (e.g., RAC, ASQ) (preferred).
Strong analytical, risk‑management, and problem‑solving skills.
Effective written and verbal communication skills.
Language: English required; additional European languages preferred.
Moderate regional travel; limited international travel.