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Director R&D Engineer Medical Device Jobs (NOW HIRING)

UL Solutions

Staff Engineer - Medical Device

Brea, CA · On-site

$115K - $160K/yr

Performs other duties as directed. Qualifications * University Degree in Electrical Engineering or related field. * 10+ years of Compliance Engineering experience as Evaluator and Reviewer in the ...

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Director R D Engineer Medical Device information

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$194.7K

$254K

How much do director r&d engineer medical device jobs pay per year?

As of Sep 3, 2026, the average yearly pay for director r&d engineer medical device in the United States is $194,709.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,500.00 and $253,000.00 per year, depending on experience, location, and employer.
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Director R D Engineer Medical Device jobs near you
Infographic showing various Director R&D Engineer Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $194,709 per year, or $93.6 per hour.

Process Validation Engineer/Manufacturing Engineer - Medical Device

Stark Pharma Solutions Inc

Raynham, MA • On-site

Contractor

Re-posted 5 days ago

Job description

Job Title: Senior Process Validation Engineer

Location: Raynham, MA (Onsite – Local candidates preferred)

Type: Contract (1 year + long-term extensions)

Industry: Medical Device Manufacturing | Supply Chain Quality

Job Summary:

We are seeking a Senior Process Validation Engineer to support the startup and qualification of a new Class III medical device manufacturing facility. This role will be part of the Supply Chain Quality team and will lead critical validation and quality activities to ensure compliant and efficient manufacturing operations.

The ideal candidate will bring strong expertise in process validation, equipment qualification, and inspection readiness, working closely with cross-functional teams in a highly regulated environment.

Key Responsibilities

  • Lead process qualification and validation activities to ensure manufacturing processes are robust and compliant
  • Plan and execute IQ, OQ, PQ, and process validation activities
  • Develop validation strategies, protocols, reports, and documentation (including URS)
  • Support inspection readiness by ensuring Critical-to-Quality (CTQ) characteristics are verified using qualified methods
  • Perform test method validation and measurement system analysis (e.g., Gauge R&R)
  • Provide Quality oversight for validation documentation and approvals
  • Support deviation investigations, root cause analysis, and troubleshooting
  • Collaborate with Manufacturing, Engineering, Supply Chain, and R&D teams to meet project timelines

Required Qualifications

  • 5+ years of hands-on experience in process validation within regulated environments (GMP/ISO)
  • 4+ years of experience in Quality, Supply Chain, or R&D within medical devices or similar industries
  • Strong expertise in IQ/OQ/PQ, process verification, and validation documentation
  • Experience with CNC machining processes and Coordinate Measuring Machines (CMM)
  • Experience in risk management (FMEA)
  • Strong communication, collaboration, and project management skills