Quality & Compliance Leader Supplier Quality Management - EMEA M/F Job

Description de l'offre

Quality & Compliance Leader Supplier Quality Management
- EMEA M/F-1500056424WDescriptionJohnson and Johnson is a globally operating health care company with nearly 130’000 people working in more than 275 companies and 60 countries across the three divisions Pharma (Janssen Pharmaceuticals), Medical Devices & Diagnostics and Consumer.
Your unique talents and perspective can make a vital contribution to innovative products that improve the lives of people everywhere. Career opportunities within Johnson & Johnson companies may provide you with an ideal setting to build your leadership experience, express your passion, and touch the world.
Role summary:The Quality & Compliance Leader Supplier Quality Management :
- is responsible and accountable for the successful development, deployment, and implementation of the Supplier Quality Management (SQM) strategy and associated policies, procedures, programs and initiatives that deliver quality/compliance, cost, and/or operating benefit to the supply chain.
- Actively partners with stakeholders, individuals and teams, and external suppliers to implement innovative solutions and continuous improvements with demonstrated and measurable business results.
Major responsabilities:Supplier selection, supplier auditing, supplier performance monitoring, supplier risk mitigation:
- Have regional quality ownership of a supplier contact and relationship, own the quality responsibility agreement between J&J and the supplier
- Manage the assigned suppliers portfolio against an acceptable GMP status and risk based approach
- Own the audit planning for the supplier and ensure timely execution and follow up
- Manage new supplier qualification and change control (selection, qualification, disengagement)
- Implement the worldwide initiatives and other quality improvements at the supplier sites
- Manage supplier quality issues (i.e. micro failures, rejects, etc.) and follow-up on-site investigations
- Support direct materials changes
- Assure a continuous improvement process of the suppliers through KPI and Management Action Plan and CAPA follow up
- Participate to supplier review meetingsBusiness support and EMEA J&J internal sites support:
- Build close partnership with Procurement, R&D, Raw Material Center, Global Packaging and support of Business continuity, Cost improvement projects, suppliers portfolio optimization and consolidation
- Support Market Engagement initiatives, new supplier selection, to achieve supplier’s qualification target
- Build strong partnership with all J&J Internal manufacturing sites and support of non-conformities, material changes, inspections, quality reviewQuality & Compliance Program:
- Involve into Global Quality & Compliance programs and transverse working group
- Build close partnership with regional and global quality counterpartsSupport to Suppliers Quality Management Review
- Leading on quality issues trending at the assigned suppliers to drive improvement actions
- Support to Supplier Quality Management quality system continuous improvementIn scope:Direct Material suppliers (raw and packaging materials, components, ingredients, chemicals, APIs) which are located in the EMEA region and which are supplying materials to EMEA based J&J internal manufacturing plants and suppliers located in the EMEA region but supply to J&J plants outside our region.
Out of scope:Contracted laboratories, service providers and transport issues or others indirect suppliersSuppliers of auxiliary / promotional materials utilized by marketing companies and sitesSuppliers of materials to EMEA based external manufacturersPermanent position. Location: Val-de-Reuil or European Consumer J&J plants (Italy, Greece, Sweden).Whether you´re launching your career or you have a strong professional background, Johnson and Johnson invite you to attend one of our virtual presentation sessions on the 26th of November. Register today! http://www.careernomics.com/jnj1511/candidates/welcome.phpQualifications
- Scientific master degree (Pharmacy, Chemistry, Engineering or related field)
- A broad and deep working knowledge of the pharmaceutical drug product (preferred) or Cosmectics (or equivalent), operating functions of quality and compliance, material supply, material handling and control, product manufacturing, and product packaging gained through:
- Auditing experience is required
- Responsibility and experience in a GMP product manufacturing plant environment is required
- 8 to10 years of pharmaceutical drug product industry (or related industry) experience
- Fluent English (spoken and written)
- Detailed understanding and application of current Good Manufacturing Practices and Agency compliance expectations
- Personal skills will be decisive: personal organization, autonomy, leadership, relational and communication skills, convictions, critical thinking, adaptability in a changing and complex environment, attention to details and overall view…)
- Quality culture and global mindsetPrimary Location:Europe/Middle East/Africa-France-Haute-Normandie-EureOther Locations:Europe/Middle East/Africa-Sweden-Skåne-Helsingborg, Europe/Middle East/Africa-Greece, Europe/Middle East/Africa-Italy-Lazio-PomeziaOrganization: Johnson & Johnson Santé Beauté France SAS (7101)Travel:Yes, 25 % of the TimeJob Function: Quality (Generalist)