Careers

Job Brief

Candela is recognized globally for its innovating energy-based technologies that change lives and our new brand embodies our continued commitment to innovating medical aesthetic treatment solutions based on solid science and effective outcomes.

We aspire to provide the highest levels of clinical, technical and customer support, and continue to build on the longstanding partnerships of trust we’ve established with physicians, their practices and the patients they treat.

Every role is important at Candela:

Candela seeks a Training and Quality System Coordinator will participate in building up the training program and processes. The Coordinator will also help drive improvements in other areas of the quality system such as Change Control, CAPA and Non-Conformance

• Planning, organizing and supporting the overall quality system and training program
• Developing and tracking metrics to achieve business goals and KPIs for the Quality System
• Developing and monitoring a means for measuring and improving training and effectiveness
• Act as a resource when developing training plans
• Support the Document Control team
• Distribute training requirements for newly hired employees and for change orders
• Participate in compliance activities, such as CAPAs, non-conformances and support internal/external regulatory audits
• Develop and maintain Quality metrics and dashboards
• Serve as a CAPA facilitator
  • Moving CAPA’s through the process
  • Ensuring all documentation is complete and all activities within the CAPA have been completed
  • Ensure CAPA due dates are met or extensions have been approved

Essential Skills to be a top contributor in this role:

• Minimum 3-5 years working in a regulated environment, preferably in the medical devices or pharmaceutical industries
• Minimum 3 years’ experience in coordinating, developing and documenting training related subjects
• Minimum 2-3 years’ experience in other areas of Quality Management Systems such as CAPA and Non-Conformance
• Experience with Quality Management System (ISO 13485) and Medical Device Regulations (21 CFR 820)
• Self-motivated, able to accomplish multiple assignments simultaneously.
• Strong organizational and problem-solving skills.
• Demonstrated competency in computer skills: MS office applications, query tools, and enterprise database systems.
• Must be able to communicate appropriately and adequately to all management levels, including group presentation experience.
• Demonstrated experience/results in Quality System tools and problem solving.
• Proficient computer skills, including Excel
• Detail-orientated