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Qa Product Release Associate Analyst

5+ years
$27.00 – $42.00 per hour
10 Sept. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

QA Product Release Associate Analyst

Job Id: 290321
Location: St. Louis, Missouri, United States
Job Type: Full-time

Company Overview

At MilliporeSigma, we innovate with science and technology to improve lives across Healthcare, Life Science, and Electronics. Our global team is driven by curiosity, diversity, and excellence—building a culture of inclusion, opportunity, and human progress.

Position Summary

The QA Product Release Associate Analyst is responsible for reviewing and releasing purchased and manufactured goods to ensure compliance with internal quality systems, industry standards, and global regulatory requirements. The role involves risk assessments, vendor document review, and product release activities to ensure safe and compliant downstream use and delivery to customers.

Key Responsibilities

Evaluate raw materials and finished products (repack/manufactured) for compliance with import/export requirements, including animal by-product (ABP) regulations.

Perform routine product assignment and release in line with analytical, packaging, and labeling specifications.

Act as a technical consultant for risk assessments and mitigation strategies related to:

Pathogenic agents

Sourcing origin

Genetically modified organisms (GMOs)

Residual solvents and heavy metals

Review vendor documentation (e.g., Certificates of Origin, regulatory questionnaires) for release and project support.

Support customer-related documentation, including supply chain declarations, affidavits, and Certificate of Origin creation.

Conduct batch review and provide usage decisions.

Physical & Work Environment

70–90% office-based (documentation, review, reporting).

10–30% engagement on production, QC, and packaging floors.

Environmental conditions vary with responsibilities.

Qualifications
Minimum:

High School Diploma or GED.

5+ years of experience in the life sciences industry.

Preferred:

Bachelor’s Degree in Life Science (Chemistry, Biology, etc.) or Engineering (Chemical, Process, etc.).

Experience with SAP (ERP) systems, particularly for COA generation and product release.

Knowledge of ISO 9001:2008 / ISO 13485.

Understanding of USDA, FDA, EC, DEFRA, ICH, EDQM regulatory frameworks.

Knowledge of animal/human pathogens.

Experience in the fine chemicals industry.

Compensation & Benefits

Pay Range: $27.00 – $42.00 per hour (based on education, skills, and experience).

Eligible for performance-based bonuses.

Benefits include: health insurance, paid time off (PTO), retirement contributions, and additional perks.

Why Join Us?

Be part of a global leader in science and technology.

Work in a diverse and inclusive environment that drives innovation.

Access growth and career development opportunities at your own pace.

Contribute to projects that impact millions and champion human progress.

👉 Apply now and join a team committed to sparking discovery and elevating humanity.