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Manufacturing Associate III Site , Redmond, WA.

Job in Redmond, King County, Washington, 98052, USA
Listing for: Evotec WD
Full Time position
Listed on 2026-06-04
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Pharmaceutical Manufacturing, Operations Engineer, Manufacturing Production
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Associate III - Days, Site Based, Redmond, WA.
Job Title:

Manufacturing Associate III - Redmond, WADayshift:
Wed-Sat

About Us:

this is who we areAt Just Evotec Biologics, 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:

/ your challenge, …in our journey

We’re looking for a passionate and curious Manufacturing Associate III 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 Manufacturing Associate III at Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.

Manufacturing Associates III are expected to execute process recipes, monitor equipment and processes, perform basic tasks, including sampling, and routine maintenance of lab equipment in support of downstream manufacturing operations. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. Manufacturing Associates III may also assist in media and buffer compounding.

What You’ll Do:

Perform and monitor critical processes (i.e., column packing, capture and polishing chromatography steps, viral inactivation, viral filtration, and UF/DF operations)
Support the introduction of new products and technologies into the facility

Initiate quality records, including but not limited to non-conformances (NC), Corrective/Preventative Actions (CAPA) and assisting in investigations.

Draft and revise Manufacturing Procedures and Standard Operating Procedures, as necessary

With minimal supervision set up, operate, and maintain a majority of MFG equipment; collects data, and writes/ updates GMP documentation.

With direction from Floor Lead/ Supervisor, propose and test solutions to MFG Operational problems. Be able to identify when a deviation has occurred.

Actively participate in departmental teams, NPI. May present run data as applicable.

Train Junior level staff

Respond to equipment alarms with help of Floor Lead.

Effectively communicate with Floor Lead/ Supervisor the status of MFG Operations.

Document operational requirements in batch records in accordance with cGMP and company guidelines

Develop an understanding of equipment and operations used to manufacture biotherapeutics in cGMP manner.

Demonstrate situational leadership within MFG and company responsibilities

Perform other duties as assigned

Who You Are:

Master’s degree; or Bachelor’s degree and 3 years of Manufacturing & Operations experience; or Associate’s degree and 5 years of Manufacturing & Operations experience; or High school diploma / GED and 7 years of Manufacturing & Operations experience

Preferred Requirements:

Single use technology experience

Capacity to develop solutions to technical issues of moderate scope

Train other personnel on equipment operation

Draft and revise SOPsProven knowledge of cGMP requirements to ensure compliance

Experience in operations required for the manufacture of biotherapeutics

Focus on quality and attention to detail

Ability to organize, analyze/interpret, and effectively communicate data and results

Motivated, self-starter with strong mechanical aptitude

Good interpersonal, team, and communication skills

Troubleshooting skills on Manufacturing equipment including single use equipment

Experience with Delta V/MES Experience with lab equipment/testing

Be open to change and manage emotions during periods of organizational change.

Why Join Us:

Growth Opportunities:
We’re a company that believes in…
Position Requirements
10+ Years work experience
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