Immediate Job Opening - Development Quality Engineer (Medical Device) - MN Apply
Hi, Please find the below job description and if you are interested send me your updated resume to saichandra@intellectt.com. Thank You.
Location: St. Paul, MN
Duration: 9+ Months (Possibility of extension)
Its an Onsite role (blended role, but need to available locally)
Job Description:
- Sr Development Quality Engineer(Must Have Medical Device)
- Support New Product Development
- Lead completion of Design Control deliverables
- Primary work is into test method validation
- Write Design verification protocols
- Coordinating traceable, analysing data
- Writing design verification reports
- A lot of Work on Risk Management, updating FMEAs and other risk documents
- Experience to understand the design development process
- Understand development Quality design assurance related deliverables and assign tasks
- Should be a core team member to represent the quality function on the team
- Responsible for all the Development Quality deliverables
- compliance to design control requirements
- Keep the track of the deliverables
- Assign deliverable to Jr Engineers
- Work with cross-functional
- Great Communication Leadership skills
- Problem-solving with CAPA experience
- Protocol designing experience
- Report writing experience
- Bachelor or Engineer (Mechanical or Bio Medical)
- 5 - 8 years of experience in R&D or Quality Role
- Mechanical device understand,
- communication and leadership
- report writing skills, reviewing documents
- Product testing
- design control deliverables
- Develop Test method, perform Test method validation
- Core team members - leadership kills
