Not specified; base pyy n/a; range may vary by loc...
Not specified (assumed standard office work)
Supervisory experience in medical device industry
Minimum 5 years of supervisory experience
Knowledge of iso13485 and fda 820 requirements
Abbott is seeking a Technical Services Supervisor in Shinjuku, Japan, responsible for managing a team that handles technical complaints and ensures regulatory compliance in the medical device industry. The ideal candidate should have supervisory experience, strong people skills, and a background in a relevant discipline
Job Summary
The Technical Support Supervisor is responsible for coordinating day-to-day operations of a Complaint Intake/Technical services team supporting assigned markets.
Abbott offers career development with an international company recognized as one of the best places to work for diversity and working mothers.
The role requires partnering with QA/RA functions to ensure adherence to the Quality Management System meeting both ISO13485 and FDA 820 requirements.
Matching Summary
Match Score: 85
Abbott is seeking a Technical Services Supervisor in Shinjuku, Japan, responsible for managing a team that handles technical complaints and ensures regulatory compliance in the medical device industry. The ideal candidate should have supervisory experience, strong people skills, and a background in a relevant discipline.
Salary
Not specified; Base pay N/A; Range may vary by location
Skills & Requirements
Must-have
Supervisory experience in medical device industry
Minimum 5 years of supervisory experience
Knowledge of ISO13485 and FDA 820 requirements
Experience with complaint regulatory compliance
Ability to manage team budgets and resources
Nice-to-have
Strong emotional intelligence and active listening skills
Proven ability to drive continuous improvement initiatives
Experience leading new product launch activities
Talent development and coaching capabilities
Cross-functional collaboration skills
Key Requirements
3rd Level Certificate, Diploma or Degree in Science, Biomedical, Engineering, or Nursing
Minimum 5 years' supervisory/team lead experience in medical device industry
Experience with process reviews and CAPA program ownership