5+ years of experience in the medical device industry
Strong analytical and problem-solving skills
Understanding of manufacturing processes
Proficient in PC applications (Microsoft Word, Excel, etc.)
Experience with Validation (IQ, OQ & PQ)
Ability to interpret engineering drawings and schematics
Responsibilities
Communicate effectively with global cross-functional teams
Drive design quality activities for new product development
Complete and approve verification and validation tasks
Validate Time Savor Fluid changes and new silkscreen ink
Create and review risk management reports and DFMEA
Benefits
Collaborative team environment
Opportunity to work on innovative medical device projects
Exposure to global client interactions
On-site role allows for direct engagement with the team
Career advancement in a specialized field
Full Job Description
Role : Design Quality Engineer Location: Warsaw, IN (On-Site)
Must have Medical Devices Exp.
Job Description:-
Strong creative, analytical and problem-solving skills.
Process experience, ability to observe and understand manufacturing processes.
Personal computer skills, Windows: word processing, presentation, e-mail, web browsers & spreadsheet software
Ability to work efficiently, meet timelines, and communicate status (generate trackers, send emails, etc.)
Good experience in Validation (IQ, OQ & PQ).
Ability to read engineering drawings, GD&T, terminology, schematics.
In-depth knowledge of design of medical devices preferred.
Roles & Responsibilities:
The candidate will need to have effective communication skills and be a team player to work with globally located client cross-functional teams to execute and deliver as per projects requirements.
The candidate will be responsible for the following.
Driving and supporting design quality activities for multiple new product development projects
Completing and approving verification and validation activities.
Time Savor Fluid change validation, New Silkscreen ink
