Responsible for design control and risk management of next-generation capital equipment devices.
Uses clinical knowledge/Data to influence how devices they are working on are tested and designed.
Responsible for the implementation and development of product risk management tools (i.e. Hazard Analysis, Fault Tree, FMEAs).
Builds quality into all aspects of work by maintaining compliance to all quality requirements.
Plans, organizes and prioritizes own daily work routine to meet established schedule.
Utilize standard statistical analysis and problem-solving techniques to determine product acceptance and evaluate process capabilities.
Apply technical skills including sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Other duties as required.
Required qualifications:
Bachelor's Degree in Engineering (Electrical, Biomedical preferred)
3+ years related working experience from Medical Device Industry
Knowledge of ISO 13485, ISO 14971, IEC 62366-1, IEC 62304
Demonstrated interpersonal skills with ability to work within a team environment
Strong written/verbal communication skills
Must be able to work independently under limited supervision
Preferred qualifications:
Six Sigma problem solving methodologies
Training experience to FDA regulations or ISO standards