CAPA and NC Manager

Own and maintain the NC-CAPA process and associated procedures Ensure compliance with requirements for control of nonconforming products Lead and facilitate investigations, root cause analysis, and definition of the associated corrective and preventive actions Train and coach a network of NC-CAPA Owners throughout the organization Lead cross-functional teams to resolve complex quality issues Ensure investigations are evidence-based, timely, and adequately documented Drive sustainable corrective actions that address true root causes Verify effectiveness of implemented actions prior to CAPA closure Present the NC-CAPA process and records during external audits Ensure CAPAs are completed within established timelines and meet regulatory and internal requirements Prepare quality metrics and reports for management review Analyze quality events and CAPA Metrics to define the appropriate strategies to eliminate Field Safety Corrective Actions Promote a culture of quality, compliance, and continuous improvement

At Medartis, we combine innovative solutions with skilled professionals to be the provider of choice in orthopaedics. Founded in 1997 and headquartered in Basel, Switzerland, the Medartis Group is one of the world’s leading manufacturers and providers of medical devices for the surgical fixation of bone fractures in the upper and lower extremities, as well as the craniomaxillofacial region. The company employs around 1,400 people across its 13 locations and sells its products in over 50 countries worldwide.

• Master's or Bachelor's degree in Engineering, Life Sciences, Quality Management, or a related technical discipline

• Minimum 5-7 years of experience in Quality Assurance or Quality Systems within the medical device industry

• Minimum 3 years of experience managing CAPA and/or Nonconformance processes

• Experience supporting regulatory inspections and external audits preferred

• Strong knowledge of ISO 13485:2016 requirements

• Understanding of CAPA, Nonconformance Management, Complaint Handling, Supplier Quality, and Risk Management processes

• Experience with root cause analysis and problem-solving methodologies

• Proficiency in electronic quality management systems (eQMS) and quality metrics analysis

• Fluent in German and English, written and spoken

• Results-oriented with strong cross-functional collaboration skills

• Excellent analytical and problem-solving abilities

• Ability to manage multiple priorities in a regulated environment