Biopharma QA Specialist — Compliance & Quality

Evotec; Redmond (WA); On-site; USD 78,000 - 82,000; Full time

Benefits offered by this job

Growth opportunities

Flexible work environment

Inclusive culture

Innovative projects

Big ideas encouragement

Job summary

Just Evotec Biologics in Redmond, WA is seeking a QA Associate to join the Quality team. The role will review batch records, support manufacturing compliance, and participate in audits and regulatory activities.

You’ll collaborate across functions to ensure product quality and regulatory readiness, driving continuous improvement in a site-based environment. The role requires a life sciences degree and 2+ years in biopharma cGMP manufacturing, with attention to detail and strong teamwork.

Qualifications

• Bachelor's degree in a life science field required.
• Minimum 2 years of biopharmaceutical/cGMP manufacturing experience.
• Strong attention to detail and cross-functional collaboration.

Responsibilities

• Review executed Manufacturing Batch Records.
• Participate in compliance walkthrough of the Manufacturing floor.
• Partner with Manufacturing to ensure compliance in operations.
• Review and approve Master Batch Records and supporting docs.
• Execute process performance and product quality monitoring programs.
• Alert senior management of deviations or compliance risks.
• Manage QA QMS processes (Deviations, Change Control, CAPA, etc.).
• Support QA QMS audits and regulatory inspections.
• Monitor QMS effectiveness via trending and KPIs.
• Act as QA representative on cross-functional product teams.

Skills

Attention to detail

Cross-functional communication

Education

Bachelor's degree in biological sciences, chemistry, biochemistry, engineering, or related life science field

Job description

Just Evotec Biologics in Redmond, WA is seeking a QA Associate to join the Quality team. The role will review batch records, support manufacturing compliance, and participate in audits and regulatory activities.

You’ll collaborate across functions to ensure product quality and regulatory readiness, driving continuous improvement in a site-based environment. The role requires a life sciences degree and 2+ years in biopharma cGMP manufacturing, with attention to detail and strong teamwork.