CQ Specialist Supplier Mgmt

Responsible for the management of assigned Quality System processes e.g. Document & Record Management, Quality Agreements, Change Control, Repack Relabel, Purchasing Controls, Audit, CAPA, training etc. Serve as an SME (Subject Matter Expert) for the assigned Quality System processes e.g. Document & Record Management, Quality Agreements, Change Control, Audit & Inspection, Repack Relabel, Purchasing Controls, CAPA, training etc… Provide guidance and support and coaching on assigned processes & systems. Ensure adequate communication of quality compliance needs and status to all affected sites/organizations. Drive simplification, standardization, and continuous improvement of processes across the EMEA region. Ensure timely and consistent reporting of metrics and KPIs (Key Performance Indicators) associated with assigned processes. Provide regional audit/inspection readiness support. Builds strategic partnerships regionally and globally, and support implementation of solutions. Perform other related duties as required. Monitors compliance with company policies and J&J; quality procedures. Evaluate quality processes and recommend improvements to meet regulatory requirements.

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.

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

• 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.

• Experience with ISO certification, Notified body; Health authority inspection experience preferred.

• Detailed understanding of QM Systems and local/regional (EMEA) Medical Device regulations.

• Understanding the linkages in Quality and Regulatory compliance in delivery to customer and health authority.

• Ability to work cross‑functionally and influence internal and external stakeholders.

• Strong analytical, organizational, and problem‑solving skills.

• Fluent in English; German preferred.

• Moderate international travel.

• Quality‑related certifications (e.g., ISO, ASQ) preferred.