Quality Assurance Product Release Analyst
Job in
Saint Louis, St. Louis city, Missouri, 63103, USA
Listed on 2026-07-03
Listing for:
Merck Group
Full Time
position Listed on 2026-07-03
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet.
That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role
The Quality Assurance Product Release Analyst plays a critical role in ensuring the timely and compliant release of purchased and produced goods s position is responsible for performing a variety of quality review functions according to established criteria and guaranteeing that products meet all necessary specifications and regulatory requirements. The Quality Product Release Analyst will collaborate with various internal stakeholders and will be a subject matter expert in QA product release processes.
Key Responsibilities:
- Provide on-the-floor quality review of finished products and labels
- Ensure that raw materials and finished goods meet analytical, performance, packaging, and labeling specifications in accordance with established acceptance criteria and regulatory requirements
- Review vendor documentation, including certificates of origin, certificates of analysis and customer and regulatory questionnaires
- Evaluate raw materials and final products to determine acceptability and compliance with import/export requirements derived from animal by-product (ABP) regulations
- Perform thorough review of production and packaging batches and determine usage decisions regarding the acceptability of materials and products
Minimum Qualifications:
- High School Diploma or GED AND 1+ year of experience in quality management systems
- Bachelor's Degree in Chemistry, Biology or other life science discipline
- Strong computer proficiency, including hands-on experience with SAP systems
- Familiarity with specialized enterprise quality management systems (eQMS) or electronic document management platforms
- Robust problem-solving and analytical skills
- Excellent written and verbal communication skills, with the ability to collaborate effectively across multiple departments
- Demonstrated ability to work autonomously, manage time efficiently, and meet deadlines
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.
For more information click here.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
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