Just Evotec Biologics

Biopharmaceutical

QAAssociate

$78–78k Redmond, Washington, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“QA Associate at Just Evotec Biologics. Review executed Manufacturing Batch Records. Participate in compliance walkthrough”

What You'll Achieve.

ensure compliance with cGMPs; ensure compliance in Manufacturing operations; assure compliance with regulatory requirements; assure compliance with G-QMS requirements; Monitor effectiveness for QMS; identify opportunities for continuous improvement

Industry & Context.

Biopharmaceutical
Problems you'll solve

solving complex problems

Eligibility Requirements

Ad-hoc days for business requirements

What They're Looking For.

Must Have

Bachelor’s degree in biological sciences, chemistry, biochemistry, engineering, or related life science field., Minimum of 2 years relevant experience in a biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment., attention to detail, Ability to collaborate and communicate cross-functionally

What You'll Do.

Review executed Manufacturing Batch Records

Participate in compliance walkthrough

Review and approve Master Batch Records

Execute process performance monitoring

Execute product quality monitoring

Initiate quality events

Review quality events

Support QA QMS in audits

Support QA QMS in inspections

Act as QA representative

How You'll Work.

Team & Collaboration

collaborate with Manufacturing, Quality and Facilities staff; Partner with Manufacturing; Act as the QA representative on cross-functional product teams

Communication Scope

communicate cross-functionally

Full Job Description

**Job Title:** QA Associate **Location:** Redmond, WA (onsite) **Shifts:** Days, Mon to Fri, 8 hour shifts, ending 16:00, with Ad-hoc days for business requirements. **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 QA Associate 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. The QA Associate role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing. This role works collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. **What You 'll Do:** * Review executed Manufacturing Batch Records. * Participate in compliance walkthrough of the Manufacturing floor and other assigned areas. * Partner with Manufacturing to ensure compliance in Manufacturing operations. * Review and approve Master Batch Records and other supporting documents. * Execute process performance and product quality monitoring programs. * Alert senior management of potential deviations or compliance risks. * Initiate and review all quality events of eQMS (Deviations, Change Control, CAPA, Risk Assessment, Management Review, Complaint Investigation, Product Quality Review etc.) to assure compliance with regulator

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