GLP QA Specialist II: Document Control & Compliance

Scorpion Therapeutics; Fall River (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

Scorpion Therapeutics is seeking a QA specialist focused on GLP quality systems within a biotech/pharma setting in Fall River, MA. You will maintain and improve GLP compliance, manage document control, and support QA reporting.

The role requires a BS in Life Sciences and 1–3 years of QA experience in biotech/pharma, with strong EDMS and MS Office knowledge, and excellent communication. You will collaborate across teams to uphold cGMP/GLP standards.

Qualifications

• BS/BA in Life Sciences required.
• 1–3 years QA experience in biotech/pharma.
• Strong knowledge of EDMS, cGMP/GLP, MS Office.
• Excellent communication skills.
• Ability to work independently and collaboratively.

Responsibilities

• Manage GLP document systems, laboratory notebooks, and QA reports.
• Support GLP testing and audits.
• Create trend reports on QA metrics.
• Partner with cross-functional teams to ensure quality standards.

Skills

Communication

Independent worker

Education

BS/BA Life Sciences

Tools

MS Office

EDMS

Job description

Scorpion Therapeutics is seeking a QA specialist focused on GLP quality systems within a biotech/pharma setting in Fall River, MA. You will maintain and improve GLP compliance, manage document control, and support QA reporting.

The role requires a BS in Life Sciences and 1–3 years of QA experience in biotech/pharma, with strong EDMS and MS Office knowledge, and excellent communication. You will collaborate across teams to uphold cGMP/GLP standards.