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**Job Function:**
Quality
**Job Sub** **Function:**
Quality Assurance
**Job Category:**
Professional
**All Job Posting Locations:**
Schaffhausen, Switzerland
**Job Description:**
Job Description
Duties & Responsibilities:
NC CAPA Quality System Investigation Process: Supply Chain Implementation
+ Support efficient and effective investigation training/certification. Support NC/CAPA system and process user training
+ Facilitate the initiation of investigations and CAPAs and monitor progress and approvals.
+ Collaborate with key stakeholders to support the end-to-end NC/CAPA process.
+ Support NC/CAPA system and process user training, including investigation certification.
+ Facilitate initiation of investigations and CAPAs and monitor progress to ensure timely completion.
+ Execute quality reviewer/approver duties, review evidence, and approve closure of NC and CAPA records.
+ Conduct investigation record quality reviews for documentation completeness, robust root-cause analysis, and compliance with procedures.
+ Monitor CAPA effectiveness and confirm root cause is eliminated or reduced to an acceptable level.
+ Use data analytics and trending to identify failure modes, measure CAPA effectiveness, and inform continuous improvement priorities.
+ Compile and provide regular CAPA status updates, metric reports, and trending analyses.
+ Collaborate with stakeholders, site owners, governance bodies, and senior management to resolve issues and align on corrective actions; escalate risks or compliance issues to the Senior Manager, Quality Systems CAPA as needed.
+ Coordinate with IMSC sites and responsible functions to drive completion of assigned actions.
+ Partner with site NC/CAPA business process owners and J&J Quality Systems Platform Governance to sustain processes and support platform enhancement requests.
+ Ensure the IMSC NC/CAPA process remains inspection-ready and support audits/inspections.
+ Provide coaching and actionable feedback to issue owners on CAPA best practices, system usage, and investigation execution.
+ Participate in and/or support internal audits and regulatory inspections, as needed.
+ Attend, participate and/or facilitate SC NC CAPA review meetings, as needed.
+ Perform other duties as necessary
Education & Experiences:
+ Bachelor’s Degree in Life Science or related discipline or equivalent is required.
+ Knowledge and experience with regulations and regulatory compliance issues.
+ Minimum of 6 years’ experience in a regulated MedTech or Pharmaceutical Quality Systems Compliance field and/or equivalent experience/training in a related NC CAPA Investigation Quality System area.
+ Demonstrated experience as an investigator of Non-Conformance/CAPA process.
+ Excellent communication and writing skills demonstrated by the ability to develop clear and concise professional correspondence.
+ Requires critical analytical and problem-solving skills, strategic thinker, and collaborator.
+ Excellent organization, prioritization, and time management skills.
+ Demonstrated competencies include adaptability, attention to detail, and ability to build and maintain relationships and partnerships across the organization.
+ Ability to build and maintain cross-functional interactions and coordination.
+ Ability to build consensus, influence, and negotiate.
+ Knowledge of Quality Management, Project Management and/or Process Excellence concepts and practices.
+ Other core skills: strong attention to detail, excellent time management, relationship-building, and experience with CAPA systems, investigative techniques, and data-driven quality improvement.
Decision-making & Problem-solving:
+ Ability to work independently and coordinate across Supply Chain driving compliance to the NC CAPA Global Process.
+ Requires basic management skills for cross-functional interactions and coordination.Facilitates resolution of issues and able to collaborate with stakeholders at varying levels of management across multiple organizations.
+ A fundamental understanding of the risk management process to engage key stakeholders and mentor colleagues to capture insights and make risk-based decisions.
+ Excellent communication and writing skills demonstrated by the ability to write executive summaries and ad hoc reports promptly and clearly as well as compile and present data to other professionals.
+ Requires data analytical skills to examine data and perform analysis.
+ Requires decision-making skills to approve the appropriateness, effectiveness, quality and compliance of documented robust investigations, root cause analysis and corrective/preventative action plans.
Working relationships/interfaces:
+ Must be able to effectively operate in a matrixed environment and interact with cross functional leaders on a regular basis.
+ Senior Manager/Director, NC CAPA – interfaces and informs as needed to discuss issues.
+ CAPA and Issue Management team members – interfaces daily as needed to manage workload, interfaces weekly in team meetings.
+ Supply Chain, Global Quality Systems, R&D Senior Management, R&D Quality, Regulatory Affairs, Medical Affairs, and other business functions involved in owning investigations and delivering CAPA commitments - interfaces as needed to address identified issues and provide guidance on established processes.
+ J&J partners – must be able to effectively interact with third-party organizations, and marketing partners as needed to address cross-company and cross-departmental issues.
**Required Skills:**
**Preferred Skills:**
Business Alignment, Business Savvy, Coaching, Communication, Compliance Management, Continuous Improvement, Fact-Based Decision Making, Human-Centered Design, ISO 9001, Issue Escalation, Problem Solving, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP)