QA Specialist I

Scorpion Therapeutics; Baudette (MN); On-site; USD 54,000 - 78,000; Full time

Job summary

Scorpion Therapeutics in Baudette, MN seeks a Quality Assurance Specialist to ensure documentation and data integrity for raw materials, finished products, and stability activities within a cGMP-regulated environment. You will review records, support validation, and help maintain compliance.

The role requires a Bachelor's degree with 2+ years in QA/QC, proficiency in HPLC data, and strong communication and problem-solving skills. On-site position with occasional travel and competitive benefits.

Qualifications

• Bachelor's degree with 2+ years in QA/QC; strong understanding of laboratory testing (HPLC), data review, and cGMP standards.
• Proficient in computer skills; experience in regulated environments; problem-solving, organizational, and communication skills.

Responsibilities

• Review notebooks, data sheets, reports, and batch records for compliance.
• Support stability, validation, and annual reporting.
• Perform product disposition, packaging audits, sample inspections, and monitor GMP areas for adherence.

Skills

QA/QC

HPLC

Data review

cGMP

Problem-solving

Organizational

Communication

Computer skills

Education

Bachelor's degree in QA/QC or related field

Job description

Role

Quality Assurance Specialist ensuring documentation and data integrity for raw materials, finished products, and stability activities within cGMP-regulated pharmaceutical manufacturing.

Responsibilities

review notebooks, data sheets, reports, and batch records for compliance; support stability, validation, and annual reporting; perform product disposition, packaging audits, sample inspections, and monitor GMP areas for adherence.

Qualifications

Bachelor's degree with 2+ years in QA/QC; strong understanding of laboratory testing (HPLC), data review, and cGMP standards; proficient in computer skills; experience in regulated environments; problem-solving, organizational, and communication skills.

HighValue

pharmaceutical manufacturing, cGMP compliance, batch record review, stability, and validation support.

WorkSetup

on-site with occasional travel; salary range $54,000-$78,000, with benefits.