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Manufacturing Associate III - Redmond, Swing Shift

Job in Union Hill-Novelty Hill, King County, Washington, USA
Listing for: Evote
Full Time position
Listed on 2026-01-16
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Pharmaceutical Manufacturing, Operations Engineer, Manufacturing Production
Salary/Wage Range or Industry Benchmark: 32.56 - 41.46 USD Hourly USD 32.56 41.46 HOUR
Job Description & How to Apply Below
Position: Manufacturing Associate III - Redmond, Days or Swing Shift
Location: Union Hill-Novelty Hill

Job Title:

Manufacturing Associate III - Redmond, WA Dayshift:
Sun-Wed  or Swing shift:
Sun - Wed 12noon - 23:00

Note:

Swing shift receives a 10% premium above base pay.

About Us:

this is who we are

At 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? #Be Cureious 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 II I 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 indepartmental 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 SOPs
  • Proven 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…
Position Requirements
10+ Years work experience
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