Catheter Process Development Tech – Medical Devices

Midwest Interventional Systems Inc; Maple Grove (MN); In loco; USD 32.000 - 39.000; Tempo pieno

Vantaggi offerti da questo lavoro

Paid time off

Company holidays

Health, Dental, Vision coverage

Disability insurance

HSA with employer contribution

401(k) with employer contribution

Descrizione del lavoro

Midwest Interventional Systems Inc in Maple Grove, MN is seeking a Process Development Technician to join our multidisciplinary engineering team. You will build and test catheters, contribute to R&D projects, and help drive the development of new therapies in a cleanroom environment.

The role requires 1+ year in the medical device field, ISO 13485 and FDA Part 820 knowledge, and strong MS Office/Excel skills.

Competenze

• 1+ years of work experience in the medical device industry.
• Experience with ISO 13485 and FDA 21 CFR Part 820.
• Proficient in MS Office and Excel; strong communication skills.
• Ability to document processes and follow procedures.

Mansioni

• Build and test catheters and sub-assemblies.
• Support R&D and commercial manufacturing lines.
• Assist with designing new catheters.
• Execute process development activities in a cleanroom environment.
• Document process settings in batch records and notebooks.
• Cross-train team members across value streams.
• Perform in-process and final inspections for quality.
• Follow cleanroom protocols and maintain tidiness.
• Collaborate with internal teams to troubleshoot and improve processes.
• Perform weekly Product Processing Area cleaning.

Conoscenze

Medical device industry experience

Verbal and written communication

Detail oriented

Independent worker

Strumenti

MS Office

Excel

Descrizione del lavoro

Midwest Interventional Systems Inc in Maple Grove, MN is seeking a Process Development Technician to join our multidisciplinary engineering team. You will build and test catheters, contribute to R&D projects, and help drive the development of new therapies in a cleanroom environment.

The role requires 1+ year in the medical device field, ISO 13485 and FDA Part 820 knowledge, and strong MS Office/Excel skills.