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PSG Global Solutions Hardware Engineer in South San Francisco, California

Hardware Engineer

Location:South San Francisco, CA, United States

Job Type:Contract

Job Category:Engineering

Job Industry:Pharmaceuticals and Medical Products

Salary:The pay we're offering is $34 - $44 per hour


We're looking for aHardware Engineer, working inPharmaceuticals and Medical Productsindustry in269 E Grand Ave, South San Francisco, California, 94080, United States.

  • Develop and run novel tests and procedures.

  • Implement and appropriately modify various ASTM standard test systems.

  • Execute rigorous system characterization and requirements verification protocols.

  • Report and communicate findings in accordance with international medical device regulatory requirements.

Our Client

Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.

Experience Required for Your Success

Basic Qualifications:

  • BS degree in Materials Science, Electrical Engineering, Mechanical Engineering, Chemistry, Chemical Engineering or equivalent practical experience

  • Experience with fixture prototyping using 3D printing, CAD, machine shop tools, etc.

  • Experience with failure analysis and associated mechanical, electrical, and chemical test equipment

  • Experience programming test systems and testing/analysis scripts (Python)

  • Experience validating novel test systems and designing novel experimental protocols

Preferred qualifications:

  • Experience with electrochemical characterization techniques, including cyclic voltammetry and electrochemical impedance spectroscopy

  • Experience with the implantable medical device regulatory approval process

  • Experience translating in vivo use conditions into meaningful bench tests

  • Working knowledge of statistics as applied to test data

  • Highly organized with excellent written and verbal communication skills, and the ability to generate clear, well-organized reports

What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?