Senior QC Analyst - Biopharma Raw Materials & GMP

Scorpion Therapeutics; Framingham (MA); On-site; USD 80,000 - 105,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior QC Analyst to establish and manage QC laboratory operations for raw materials in biopharma manufacturing, ensuring material quality and GMP compliance. You will lead routine and non-routine testing, develop identity methods, review data, and support audits in a fast-paced facility.

The role emphasizes setting up labs, sample management, SOP writing, and validation activities to uphold rigorous quality standards in biologics production.

Qualifications

• BA/BS in Chemistry/Biochemistry or related science;
• 3-5 years GMP laboratory experience with strong analytical skills; familiarity with industry testing requirements for raw materials.

Responsibilities

• Set up and stock QC labs.
• Perform routine and non-routine testing (e.g., pH, ELISA, spectroscopy).
• Manage sample shipments to external labs.
• Establish identity testing methods.
• Review data.
• Write SOPs and protocols.
• Participate in equipment validation.
• Support audits.

Skills

Analytical skills

Attention to detail

Documentation

Education

Bachelor's degree in Chemistry or Biochemistry

Tools

ELISA

pH testing

Spectroscopy

Job description

Scorpion Therapeutics seeks a Senior QC Analyst to establish and manage QC laboratory operations for raw materials in biopharma manufacturing, ensuring material quality and GMP compliance. You will lead routine and non-routine testing, develop identity methods, review data, and support audits in a fast-paced facility.

The role emphasizes setting up labs, sample management, SOP writing, and validation activities to uphold rigorous quality standards in biologics production.