Position at Prismatik Dentalcraft, a subsidiary of Glidewell
Essential Functions:
- Leads the ongoing implementation of Quality Management System (QMS) in conformance with US FDA Quality System Regulations and ISO 13485 Design Controls, through the integration of internal and external/medical device industry best practices.
- Responsible for the administration of the QMS software.
- Conducts investigations and provides corrective and preventive actions based on analysis and review. Provides and implements effective solutions that will drive continuous and measurable improvements.
- Integrates ISO 14971, risk management and IEC 62366 usability engineering activities with Glidewell/Prismatik processes.
- Mentors and provides direction to software development teams in design controls and lead risk management activities.
- Fosters and maintains organizational compliance to the quality system including ongoing training and education on software QMS and Prismatik framework.
- Provides CAPA, complaints, audit and overall QMS support in regards to software.
- Performs other related duties and projects as business needs require at direction of management.
Minimum Qualifications:
- Bachelor’s degree in Engineering, Biomedical, or related technical field or equivalent practical experience.
- Minimum of eight (8) years of related experience in the FDA QSR/ISO 13485 medical device industry.
- Advance knowledge with development and test requirements with recognized standards (ISO 13485).
- Demonstrated knowledge of the application of regulatory requirements for wellness, low-risk and high-risk software applications using a scalable approach to the Prismatik practices and the QMS.
Pay range: $100,000-$130,000/yr
Exact compensation may vary based on skills and experience.
Job Type: Full-time
Pay: $100,000.00 - $130,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Retirement plan
- Vision insurance
Compensation package:
Application Question(s):
- What are your salary expectations?
- Will you now, or in the future, require sponsorship for employment visa status (e.g. H-1B visa status)?
Experience:
- ISO 13485: 1 year (Preferred)
- design control: 1 year (Preferred)
- Quality management: 1 year (Preferred)
Ability to Commute:
Ability to Relocate:
- Irvine, CA: Relocate before starting work (Required)
Work Location: In person