Senior QA Associate — GMP Biopharma (Onsite) | Equity

Scorpion Therapeutics; Bothell (WA); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Equity Incentive Plan

Annual bonus opportunity

Job summary

Scorpion Therapeutics is seeking a Quality Assurance Senior Associate to support manufacturing in Bothell, WA. The role requires hands-on QA tasks, review and approval of batch records, COAs, deviations, CAPAs, and change controls, with strong cross-functional collaboration.

Candidate should have 4–6+ years in GMP biopharmaceutical operations (2+ in GMP quality), proficiency with digital GMP platforms, and a BS degree in a related field.

Qualifications

• BS degree in biochemistry, chemical engineering, bioengineering, or related.
• 4–6+ years in GMP biopharmaceutical operations, including 2+ years in GMP quality.
• Experience with electronic quality management systems (deviations, CAPAs, change management).
• Experience with clinical manufacturing and cGMP.

Responsibilities

• Execute day-to-day QA tasks to support manufacturing.
• Review/approve electronic batch record comments and COAs; resolve discrepancies.
• Review/approve test results; perform LIMS review tasks.
• Provide QA support in cleanroom manufacturing operations.
• Serve as QA point of contact for process escalations and resolution.
• Perform hands-on QA activities: intake of patient apheresis and drug product pack-out.
• Compile/review/approve lot disposition records.
• Review/approve deviations, CAPAs, changes, excursions and nonconformances.

Skills

Quality Assurance

GMP experience

Cross-functional collaboration

Regulatory documentation

Analytical skills

Education

BS degree in biochemistry / relevant field

Tools

LIMS

Digital GMP platforms

Job description

Scorpion Therapeutics is seeking a Quality Assurance Senior Associate to support manufacturing in Bothell, WA. The role requires hands-on QA tasks, review and approval of batch records, COAs, deviations, CAPAs, and change controls, with strong cross-functional collaboration.

Candidate should have 4–6+ years in GMP biopharmaceutical operations (2+ in GMP quality), proficiency with digital GMP platforms, and a BS degree in a related field.