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QC Associate Scientist, Raw Material Inspection and Sampling - Site Based, Redmond, WA

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Job Id JOB ID-13834 Standort Redmond, Washington Veröffentlichungsdatum 03/25/2026 Job Kategorie Research & Development

Job Title: QC Associate Scientist - Raw Materials

Shifts: Days, Monday to Friday, 8:00am - 4:30pm. some flexibility required.

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?   #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 QC Associate Scientist 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 QC Associate Scientist at Just Evotec Biologic, 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.

This role will be responsible for supporting the QC Raw Materials program by inspecting and sampling incoming GMP raw materials and manufacturing supplies, performing related equipment cleaning and maintenance, and providing documentation support. In addition, the Associate Scientist will partner with Manufacturing, Materials Management, Quality Assurance, Procurement, QC staff, and outsourced testing laboratories to meet business goals and compliance requirements. As a key member of the QC group, the successful candidate will have experience with good documentation practices (GDP), be detail oriented, internally motivated, and skilled at working independently. Experience with fume hoods, laminar flow hoods, balances, aseptic technique, and cleanroom gowning is highly desired. The ideal candidate has strong written and verbal communication skills, multitasks effectively, and works well both independently and in teams.

This position reports directly to the Senior Manager of Quality Control Raw Materials.

What You’ll Do:

  • Execute the daily activities (in warehouse, laboratory, and cleanroom environments) of the QC Raw Material group in support of inspection, sampling, and testing as per written specifications and compendial methods
  • Inspect material containers, labels, and associated documentation for integrity and compliance with written specifications

  • Initiate investigations for any container integrity or compliance issues found during the inspection/sampling process

  • Manage inventory of raw material samples

  • Coordinate attribute testing (internal or external) for batch release

  • Maintain lab spaces and supply stocks

  • Provide subject matter expertise during internal project team meetings

  • Support investigation and closure of deviations, CAPAs, etc.

  • Collaborate with Quality Assurance, Manufacturing, Materials Management, and other functions to ensure internal timelines, testing TAT, and team milestones are achieved

  • Use various software tools to support tracking of material release status (Excel, SAP, LIMS, etc.)

  • Safely use laboratory equipment and instruments (e.g., FTIR, pH meter, osmometer, etc.)

  • Maintain a clean and organized work area to ensure material segregation and prevent cross contamination

  • Assist senior colleagues with reagent preparation and equipment maintenance, as necessary

Who You Are:

  • BS Chemistry or related science with related experience, or

  • AS Chemistry with 1 + years related experience

Required Qualifications:

  • Strong adherence to data integrity requirements

  • Knowledge of current instrumentation and procedures used in an analytical laboratory

  • Knowledge of Material Safety Data Sheets and appropriate safety precautions

  • Ability to follow detailed written procedures

  • Legible penmanship

  • Ability to perform multiple tasks simultaneously, manage time effectively, and adapt to changing priorities

  • Ability to succeed with minimal supervision

  • Must demonstrate initiative, resourcefulness, and flexibility to work independently and as part of a team

  • Ability to interact constructively with co-workers

  • Demonstrated meticulous attention to detail and sense of craftsmanship

  • Ability to lift up to 60 pounds; kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, and reaching without accommodation

  • Ability to routinely wear applicable personal protective equipment (PPE)

  • Ability to work with various laboratory cleaning agents and chemicals

  • Ability to train on and wear a respirator, as applicable

  • Tolerance of exposure to cold-room (2-8°C) conditions

  • Tolerance of medium noise levels

Preferred Qualifications:

  • Experience in a quality control or production environment in a cGMP facility

  • Experience in a raw materials testing or chemistry laboratory

  • Experience with aseptic technique

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.

  • Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. This role is site based.

  • 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 Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.

Are You Still Curious?

If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of Just Evotec Biologic.

Let your curiosity guide your career—#BeCurious and explore the endless possibilities at Just Evotec Biologic!

The base pay range for this position at commencement of employment is expected to be $78,000 to $83,000; this is a salary non-exempt role. Base salary offered may vary depending on the individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, generous paid time off and paid holiday, wellness and transportation benefits.

Evotec (US) Inc. is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

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