OVERVIEW

We are seeking a highly motivated and experienced Process Engineer III to lead multi-product project execution, manufacturing support, and technology transfer efforts at our Rancho Dominguez facility. This role provides technical leadership at the site level while collaborating closely with our global engineering network to deliver strategic initiatives.
The ideal candidate has a strong background in manufacturing, with expertise in process engineering, equipment qualification, and preferably within GMP or ISO 9001 environments. Success in this role requires technical proficiency, a collaborative mindset, and the ability to drive projects with minimal oversight.

QUALIFICATIONS

Education and/or Work Experience:

• Bachelor’s degree in Engineering required.
• 5-7 years of experience in medical devices, aerospace, pharmaceuticals, or biologics manufacturing.
• Hands-on experience with:
• Process validation and equipment qualification
• SolidWorks/CAD, MS Office, and electronic file management systems.
• Tech transfer between sites
• Data analysis and automation
• Filtration systems (Tangential Flow Filtration (TFF), Hollow Fiber, Flat Sheet Membranes)
• Strong knowledge of ISO 9001 and GMP manufacturing standards.
• Familiarity with single-use systems, sterilization techniques, and lean manufacturing principles preferred.
• Demonstrated ability to lead cross-functional teams and manage projects in a matrixed organization.
• High level of personal integrity, adaptability, and leadership by example.

Other requirements:

• Capable of independently defining and executing projects.
• Provides technical direction and feedback to teams across disciplines.
• Balances day-to-day plant support (40%) with project execution (60%).
• Communicates clearly with senior leadership on project scope, risks, and progress.
• Delegates tasks effectively and contributes to team development.

Physical Requirements:

• Regular work in cleanroom and laboratory environments.
• Exposure to chemicals, mechanical systems, and occasional electrical hazards.
• May be required to lift up to 50 lbs and operate in areas with noise and vibration.

• Act as a Subject Matter Expert for Tangential Flow Filtration (TFF) and other bioprocessing manufacturing systems.
• Lead projects in equipment design, tech transfer, process validation, and facility upgrades.
• Conceives, plans, and executes projects or aspects of projects related to the strategic needs of the company.
• Partner with global engineering teams to support corporate initiatives and site expansion.
• Identify and implement process improvements, ensuring compliance with industry standards and regulations.
• Develop and maintain engineering documentation including test protocols, change controls, and technical reports.
• Guide the integration of new products and manufacturing processes, supporting early-phase development through commercialization.
• Mentor junior team members and support standardization and training of best practices.
• Apply statistical tools to support validation and process optimization efforts.
• Drive innovation in filtration systems and related support infrastructure to enhance performance and scalability.