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Process Engineer II - Global MSAT Downstream​/Technology Team

Job in Union Hill-Novelty Hill, King County, Washington, USA
Listing for: Evote
Full Time position
Listed on 2026-02-28
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: Union Hill-Novelty Hill

Job Title: Process Engineer II - Global MSAT Downstream

Location: Redmond, WA

Reports to: Director, Technical Operations

About Us:

At Just‑Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward‑thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged, it’s celebrated.

Are you someone who asks questions, seeks answers, and isn't afraid to go deeper?#BeCureious with us and see where your curiosity can take you!

The Role:

We’re looking for a passionate and curious Process Engineer II to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.

As a Process Engineer II at Just‑Evotec, you will support the design and development of new equipment and technologies for the Just‑Evotec manufacturing network. The role will develop the support documentation for implementation of the technology and provide technical support to Just‑Evotec’s Site MSAT and Manufacturing Operations groups.

What You’ll Do:
  • Work with key stakeholders to evaluate new and existing technologies to increase efficiency and facility throughput.
  • Develop design documents (user requirement specifications, software functional specifications) based on platform process requirements and validation commissioning and qualification protocols.
  • Assist project leads and automation team with integrating equipment and technologies into the Distribute Control System (DCS) with the manufacturing suite.
  • Facilitate procurement and implementation of approved new technologies.
  • Lead the development equipment maintenance & life cycle plans.
  • Partner with Site MSAT Manufacturing Technology & Science team on global and site objectives.
  • Participate in Non‑Conformance investigation and provide process impact evaluations of equipment issues.
  • Participate in exchange of technical problems and solutions throughout the manufacturing network.
  • Participate in internal and external audits/inspections.
Who You Are:
  • BS in engineering, sciences, or related life science engineering 2-5 years of relevant experience in Pharmaceutical, Biotech, or Life Sciences industries, or an MS degree.
  • Working knowledge of cGMP manufacturing and regulatory regulations and requirements for biologics/pharmaceuticals.
  • Solid understanding of monoclonal antibody processing either at manufacturing scale or in process development.
  • Experience working with single‑use disposable manufacturing systems.
  • Working knowledge of manufacturing process equipment and automation systems.
  • Candidate must possess strong focus on quality and attention to detail as well as effective task/ time management organizational skills.
  • Ability to organize, analyze/interpret, and effectively communicate process data.
  • Good interpersonal, team, and collaborative skills are a must.
  • Excellent oral and written communication skills.
Additional

Preferred Qualifications:
  • Practical experience or knowledge downstream and disposable manufacturing technologies either at manufacturing scale or at bench‑scale.
  • Applies knowledge to solve complex technical problems.
  • Technical resource for Downstream Manufacturing process and platform.
  • Can work independently and in project teams.
  • Ability to navigate global regulatory CMC documents.
  • Proficiency developing and executing commissioning/qualification (CQV) plans and protocols.
  • Experience with Delta

    V for process control.
Why Join Us:
  • Growth Opportunities
    :
    We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
  • Inclusive Culture
    :
    We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
  • Innovative Projects
    :
    You’ll have the chance to work on groundbreaking initiatives and cutting‑edge technology in an atmosphere where your curiosity is the key to success.
  • A…
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