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Quality Assurance Specialist

Job

BUCKTAIL MEDICAL CENTER

Bellefonte, PA (In Person)

Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 7/5/2026

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Job Description

Quality Assurance Specialist Bellefonte, PA 1 DAYS AGO 22618123 Summary Bellefonte, PA In-Person Competitive Salary 1 Years Experience Bachelor's degree No Commission 40.00 hours per week / Day Shift / Full-Time Description Work Your Magic with us! Start your next chapter and join MilliporeSigma. 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 Specialist in Bellefonte, PA ensures that all aspects of product and service meet quality standards.
Job duties include:
Support the site's quality management system, ISO accreditations, and regulatory compliance by executing internal/external audits, changing controls, validations, document control, and customer complaint investigations. Review completed batch records for compliance and execute the Management of Change (MOC) process for quality-related modifications to documents, equipment, specifications, and methods. Participate in internal and supplier audit programs by issuing post-audit reports, maintaining the customer audit database, and tracking corrective actions through to final effectiveness checks. Monitor and trend critical quality metrics-including pass rates and customer complaints-while directly responding to client inquiries and managing quality-related customer ratings. Write and/or review documentation to ensure compliance to all standards or regulations Coordinate site validation activities and provide strategic oversight to the calibration department to ensure continuous equipment compliance. Engage regularly with production and laboratory personnel to ensure seamless communication of quality services, while leading root cause analyses and risk assessments for process and product investigations. Lead process improvement projects within the document control system to drive operational efficiencies, while continuously updating and optimizing departmental quality metrics. Coordinate the design and execution of quality training programs to support continuous employee development and maintain site-wide regulatory compliance. Maintain the quality actions and look for trends 5% travel anticipated Who You Are Minimum Qualificat To view the full job description please use the link below.
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