Senior Quality Control Analyst

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

Role

Senior QC Analyst responsible for establishing and managing QC laboratory operations and testing programs for raw materials in biopharma manufacturing. Primary objectives include ensuring raw material quality and compliance to GMP standards.

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

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.

Preferred

experience with biological raw materials, GMP environment, and water testing.

High-value details

role supports biopharma manufacturing, likely related to immunotherapy or oncolytic platforms, with a focus on raw material testing and GMP compliance.

Location

Framingham MA, onsite 5 days/week.