Scientist II, Quality Control

Scorpion Therapeutics; Framingham (MA); On-site; USD 85,000 - 120,000; Full time

Job summary

Scorpion Therapeutics is seeking a Scientist II, QC Analytical for our on-site Framingham, MA facility. This role ensures GMP-compliant testing of raw materials, in-process samples, water, and finished drug products within a cGMP environment.

The candidate will establish QC procedures, review data, manage lab systems, and generate method qualification reports. Travel is not specified; a 5-day workweek is implied by site practices.

Qualifications

• BA or BS in analytical chemistry or related science.
• 5+ years GMP/GLP laboratory experience.
• Proficiency with MS Office; strong organization and communication.
• Ability to work independently and collaboratively.

Responsibilities

• Perform GMP-compliant QC testing of raw materials, in-process, water, and drug product samples in a cGMP environment (Framingham).
• Establish and maintain QC procedures, review data, manage lab systems and equipment, generate method qualification reports, and oversee sample handling and storage.
• Support audits and regulatory inspections; troubleshoot analytical methods and equipment.
• Oversee junior staff, provide training, and assist with lab investigations such as OOS and OOT deviations ensuring GMP compliance.

Skills

GMP/GLP labs

Analytical chemistry

Data analysis

MS Office

Education

Bachelor's degree in analytical chemistry

Tools

LIMS

HPLC/GC

Job description

Scientist II, QC Analytical

Role: Scientist II, QC Analytical, responsible for performing GMP-compliant QC testing of raw materials, in-process, water, and drug product samples in a cGMP environment, primarily at the Framingham site.

Responsibilities include establishing and maintaining QC procedures, reviewing data, managing laboratory systems and equipment, generating method qualification reports, and overseeing sample handling and storage. The role involves supporting audits, regulatory inspections, and troubleshooting analytical methods and equipment. The scientist may oversee junior staff, provide training, and assist with lab investigations such as OOS and OOT deviations, ensuring GMP compliance.

Qualifications: BA or BS in analytical chemistry or related science; 5+ years experience in GMP/GLP labs with knowledge of analytical techniques; proficiency in MS Office, good organizational and communication skills; ability to work independently and collaboratively.

Preferred skills include experience with USP/EP testing, lab validation, and technical studies with external vendors.

High-Value: Focused on biologics or oncolytic immunotherapies, emphasizing GMP, quality control, and regulatory compliance within a biopharma manufacturing setting.

Location: On-site in Framingham, MA, with a 5-day workweek; travel expectations not specified.