Senior Process Engineer

Primary Talent Partners; Irvine (CA); On-site; USD 100,000 - 125,000; Full time

Job summary

A leading company in medical device manufacturing is seeking a Senior Process Engineer for a 10-month contract in Irvine, CA. The role involves developing manufacturing processes and ensuring compliance with regulatory standards. Ideal candidates will have a Bachelor's degree in Engineering and extensive experience in the medical device industry, particularly in manufacturing and process validation.

Qualifications

• 4+ years of experience in medical device industry.
• Knowledge of processing materials associated with medical devices.
• Experience with manufacturing line layout and capacity analysis.

Responsibilities

• Develop new manufacturing processes and procedures.
• Manage required builds for new product development.
• Comply with FDA and international regulatory standards.

Skills

Medical device experience

Manufacturing experience

Process validation

Good verbal and written communication skills

Computer literacy

Education

Bachelor's degree in Engineering

Tools

SolidWorks

Job description

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Primary Talent Partners provided pay range

This range is provided by Primary Talent Partners. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$55.00/hr - $65.00/hr

Primary Talent Partners has a 10-month contract opening for a Senior Process Engineer to join a large medical device company for a position operating out of Irvine, CA.

Pay: $55 - $65/hr, based on experience
Contract: 10 months, extensions likely, conversion possible
Type:W-2, cannot support C2C or provide visa sponsorship

TOP SKILLS:

Previous medical device experience

Hands-on experience in manufacturing (preferably medical device)

Process validation experience

PRIMARY RESPONSIBILITIES:

• Develop new manufacturing processes, procedures, inspection methods, and production layout for assemblies for New Product Introductions through frequent interaction with R&D, Quality Engineering, and Operations using project management, design for manufacturability, and lean methodologies.
• Develop fixtures, tooling, and equipment.
• Develop process specifications which ensure user needs are met.
• Perform equipment and process characterizations and qualifications (IQ/OQ/PQ).
• Manage required builds for new product development in a pilot or production setting, including training of operators, coordination with production planning, preparing manufacturing procedures and work orders, ordering materials, installing fixtures and equipment, supervising builds, and troubleshooting assembly issues.
• Comply with applicable FDA and international regulatory laws/standards.
• Perform other duties as assigned or required.

MINIMUM QUALIFICATIONS:

• Bachelor's degree in Engineering (preferably Mechanical, Electrical, or Biomedical)
• 4+ years of experience developing products and/or manufacturing processes in medical device industry
• Knowledge of SolidWorks and engineering statistics
• Good verbal and written communication skills
• Computer literate; word processing, spreadsheets

PREFERRED QUALIFICATIONS:

• Knowledge of processing materials associated with medical devices such as Polymers (nylons, polyethylene, polypropylene, PEEK, PTFE, FEP, etc.), and Metals (nitinol, platinum, stainless steel, etc.)
• Hands-on experience with processes associated with medical manufacturing such as shrinking (reflow), laser bonding, laser welding, thermal bonding, adhesive bonding, braiding, coil winding, hydrophilic coating, plasma treatment, cleaning processes, crimping, heat setting, electropolishing, swagging, etc.
• Experience with manufacturing line layout, capacity analysis, and line balancing.
• Process background (development, capability, optimization, validation) within a regulated industry.
• Proficient with development and qualification of fixtures/tooling/equipment (IQ/OQ/PQ, support, design).
• Experience working with outside OEM Suppliers in component development, and selection of equipment and processes.
• Experience with design and process FMECA, process validation, and process control.
• Experience being on project teams tasked with new product development and successful transfer into manufacturing.
• Knowledge of design for manufacturability and lean methodologies.

Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.

If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us [e-mail]

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Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Management and Manufacturing

• Industries

  Medical Equipment Manufacturing

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