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Director R&D Engineer Medical Device Jobs in California

TEEMA

Lead Swift/iOS Medical Device SWE

San Diego, CA · On-site

$175K - $210K/yr

Lead iOS (Swift) Software Engineer - Medical Device Startup We're partnering with a well-funded, fast-growing startup to hire a Lead iOS/Swift Software Engineer. This is a high-impact, full-time role ...

MaxLinear, Inc

Director of Device Engineering

Irvine, CA · On-site

$187 - $225/hr

Responsibilities MaxLinear is seeking a Director of Device Engineering to join our team. In this ... Lead R & D in semiconductor device engineering, especially in device characterization for both RF ...

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Medical Device Assembler

San Clemente, CA · On-site

$22.10/hr

Work under direction from management or engineering staff with direct oversight * Other duties as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

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Infographic showing various Director R&D Engineer Medical Device job openings in California as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 2% Temporary, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Sustaining / Process Engineer Medical Device

AngioSafe

San Jose, CA • On-site

$120K - $160K/yr

Full-time

Re-posted 17 days ago

Job description

Role: Sustaining / Process Engineer Company: AngioSafe Location: San Jose, CA Position Type: Full-Time on site

Overview:

AngioSafe is a Bay Area start-up focusing on improving healthcare delivery through state-of-the-art catheter development. Our seasoned experts are committed to producing high quality and innovative products to decrease risk and improve outcomes of arterial disease.

We are seeking a Manufacturing/Process Engineer to support the production and improvement of our innovative catheters ensuring high reliability, regulatory adherence, and cost-effective manufacturability. This is a hands-on role requiring direct involvement with manufacturing equipment. Candidates with primarily theoretical or design-only backgrounds will not be a fit.

Roles and Responsibilities:

  • Primary focus: Support the manufacturing line and advance the processes and device in order to support scale up.
  • Create and document new manufacturing processes as necessary for production at significantly higher volumes and validate as appropriate
  • Support ongoing manufacturing activities including dealing with production equipment, non-conformances, facilities and other line related issues. This includes SOLVING issues with laminators, laser welders, hot boxes, etc.
  • Spending significant time on the manufacturing line alongside the assemblers to improve processes and increase quality. You are the primary interface between engineering and production.
  • Assist development of assembly and test fixturing with a focus on quality and volume
  • Write protocols & test reports related to validation activities
  • Collaborate with existing suppliers to improve manufacturability and decrease cost
  • Qualify components from new suppliers in order to improve supply chain flexibility

Skills, Experience, & Behaviors:

  • Solid history of experience in a medical device manufacturing environment (~5+ years preferred)
  • Hands-on mechanical aptitude with direct experience working on production equipment is required
  • Solid experience with either lamination or laser welding is required
  • Proficiency in SolidWorks is helpful but not required
  • Proven experience editing Manufacturing Procedures (MPs), Lot History Records (LHRs), Bills of Materials (BOMs), etc. is required
  • Comfort using inspection and test equipment (vision systems, tensile testing) is a plus
  • Experience working within and maintaining compliance in a highly regulated environment
  • Demonstrated ability to work independently in a fast-paced, small company environment
  • Flexibility and willingness to take on a variety of roles
  • Demonstrated ability to collaborate effectively, especially with a team of diverse assemblers
  • Strong verbal and written communication skills.

    No relocation or immigration support provided for this role.

    Principals only Please

    AngioSafe is committed to a diverse workplace and is committed to equal opportunity employment for all job applicants without regard to race, color, religion, sex, sexual orientation, age, gender, gender identity or expression, size, national origin, disability, or veteran status. AngioSafe complies with all applicable local, state, and national laws governing non-discrimination in employment.

    Employment Type: FULL_TIME

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