Quality Control Laboratory Analyst (Raw Materials)

Scorpion Therapeutics; Pittsburgh (Allegheny County); On-site; USD 65,000 - 90,000; Full time

Job summary

Scorpion Therapeutics is seeking a Quality Control Analyst to oversee raw materials and product testing in the manufacture of gene therapies at our Pittsburgh facility. The role focuses on cGMP-compliant testing, data review, and documentation to ensure product quality.

The position requires a life sciences degree and hands-on experience with QC procedures, SOPs, and laboratory instrumentation. On-site work in Pittsburgh is expected, with opportunities to contribute to investigations and

Qualifications

• Bachelor’s degree in life sciences or related field.
• Experience with pH, osmolality, endotoxin testing; cell culture and FBS testing preferred.
• Proficient in SOP adherence, scientific writing, and MS Office.

Responsibilities

• Perform cGMP material inspections and testing.
• Review analytical data for compliance.
• Participate in investigations and protocol/report development.
• Update QC documentation.
• Support document control and USP standards.
• Maintain laboratory equipment.

Skills

SOP adherence

Scientific writing

pH testing

Endotoxin testing

Cell culture

FBS testing

Osmolality testing

Education

Bachelor's degree in life sciences or related field

Tools

MS Office

Job description

Role:

Quality Control Analyst responsible for raw materials and product testing in the manufacture of clinical and commercial gene therapies.

Responsibilities:

• perform cGMP material inspections and testing
• review analytical data for compliance
• participate in investigations and protocol/report development
• update QC documentation
• support document control and USP standards
• maintain laboratory equipment

Requirements:

• Bachelor's in life sciences or related field; experience with pH, Osmo, Endotoxin, cell culture, FBS testing preferred; proficiency in SOP adherence, scientific writing, and MS Office.

HighValue:

focus on gene therapy manufacturing, cGMP compliance, in-house raw material and finished product testing, laboratory investigations, and quality documentation.

WorkSetup:

If not specified; likely on-site at Pittsburgh facilities.