Technical Project Manager - Medical Devices, Full Lifecycle

Element Science, Inc.; Houston (TX); On-site; USD 140,000 - 160,000; Full time

Benefits offered by this job

Stock options

Medical/dental/vision coverage (90%‑em

Life insurance

401(k)

Paid time off

Paid holidays

FSA/HSA

Employee assistance program

Job summary

Element Science, Inc. is seeking a Technical Project Manager to lead cross‑functional medical device initiatives across the full product lifecycle—from early R&D through design transfer, manufacturing, and commercialization.

You will work with Engineering, Quality, Regulatory, Clinical, Manufacturing, and Operations to ensure high standards of safety, reliability, and patient impact. The ideal candidate has hands‑on experience guiding devices from concept to market, a strong regulatory

Qualifications

• Bachelor's degree in Electrical, Mechanical, Biomedical, or Systems Engineering.
• 5+ years in medical device PM across full lifecycle (R&D through post‑market).
• Proven ability to translate requirements into executable project plans.
• Strong knowledge of design controls, design transfer, and regulatory expectations.

Responsibilities

• Lead cross‑functional projects from R&D through commercialization.
• Coordinate with engineering, quality, regulatory, clinical, manufacturing, and operations teams to maintain alignment.
• Drive readiness for design reviews, verification/validation, manufacturing readiness, and launches.
• Manage risks and drive on‑time delivery with high quality and patient safety.

Skills

Technical PM

Cross-functional leadership

Regulatory awareness

Education

Engineering degree

Job description

Element Science, Inc. is seeking a Technical Project Manager to lead cross‑functional medical device initiatives across the full product lifecycle—from early R&D through design transfer, manufacturing, and commercialization.

You will work with Engineering, Quality, Regulatory, Clinical, Manufacturing, and Operations to ensure high standards of safety, reliability, and patient impact. The ideal candidate has hands‑on experience guiding devices from concept to market, a strong regulatory