Seeking an Engineering professional with experience in design control documentation, medical device product development, and hands-on manufacturing support. This is a high-impact role with future growth opportunity, equity potential, and performance bonus potential.
Key Responsibilities
- Support development and design processes aligned with ISO and FDA standards
- Assist in product testing activities and creation of related manufacturing documentation
- Build prototypes, assist in tooling development, and source components as needed
- Create and support FMEA and execute V&V (Verification & Validation) requirements
- Work cross-functionally to identify gaps and implement corrective / improvement actions
- Participate in designing and building manufacturing equipment; drive continuous improvement
- Lead or support engineering projects and product enhancement initiatives
- Present technical findings and recommendations to leadership
Required Skills & Background
Engineering and / or manufacturing process backgroundStrong analytical skills and ability to interpret data to support decision makingAbility to manage projects independently, prioritize workload, and meet deadlinesStrong written & verbal communication skills for cross-functional collaborationPosition Type : Full-Time, On-Site
Compensation Range : $70,000 - $100,000 per year (based on experience)
Benefits Offered
401(k)Medical, Dental, Health InsurancePTO (Paid Time Off)Experience Preferred
1+ year in medical device industry (preferred)