This position will focus on Quality system compliance and Process development in the contract manufacturing of medical products.
Active participant who can manage multiple and dynamically changing projects on time, while influencing change and compliance to Quality System requirements.
Position requires skills in advanced Quality Engineering techniques including; Problem solving using Six Sigma methodology, Process Validations, Process Development and optimization, Gage R&R, reducing dependence on inspection, ISO 13485 and/or 21CFR820 compliance.
- Work with and lead cross functional teams utilizing the Product Development Process to ensure robust systems and controls are in place to produce defect free product while meeting business objectives and customer expectations.
- Influence change and ensure understanding and compliance to 21CFR820, ISO 13485 and the Product Development process
- Drive and participate in Continuous improvement and Process validation activities using DOE’s, FMEA’s, Quality Plans, Gage R&R and other Quality tools
- Work through unique and/or adverse situations, gather and review information from diverse functional areas, and make appropriate quality recommendations based on facts
- Review and approve protocols, validation documents, investigations and procedure
- Provides support by conducting investigations and assisting in data and information collection as required for quality events
- Interfaces as a subject matter expert with the FDA and other government agencies during site inspections.
- Responsible for the development of process and quality procedures.
- Implement Continuous improvement methodology and metrics in cell(s) to improve business metrics
- Customer liaison for all quality related issues.
- Mentor and train other engineers/technicians in quality methodologies and regulatory requirements.
- Proactively develop improvement ideas based on experienced assessment of departmental and company performance
- Represent Quality in project team meetings and on assigned projects
- Minimum 10 years’ experience in a Quality Engineering role for a medical device manufacturer and/or start-up company
- Demonstrated technical writing and communication skills.
- Working knowledge of Statistical software and/or Minitab
- Bachelor’s degree or equivalent experience
- CQE and/or Six Sigma Green or Black belt
- BS degree; Physics, Optics, Mechanical, Chemical, Plastics preferred
- Cardiovascular experience a plus
- Demonstrated expertise in one or more of the following: ISO 13485, 21 CFR 820, Lean Manufacturing, Six Sigma
- Light office work only.
If qualified, apply now. Job title and job location must be included in the application.
To apply for this job, email your details, the job title and job location to firstname.lastname@example.org
Limitations And Disclaimer:
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties and skills required for the position. Requirements are representative of minimum levels of knowledge, skills and/or abilities. To perform this job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.