Senior Quality Assurance Specialist

4 weeks ago


Akron, Ohio, United States Bristol-Myers Squibb Full time
Job Summary

At Bristol Myers Squibb, we are seeking a highly skilled Senior Quality Assurance Specialist to join our team. As a key member of our Quality Assurance department, you will be responsible for ensuring the quality of our manufacturing processes and products. This is a unique opportunity to work in a dynamic and fast-paced environment, where you will have the chance to make a real impact on the lives of patients.

Key Responsibilities

Author and revise GMP documents as needed
Assist in executing change controls where needed
Create tutorials to help end-users train on a variety of activities
Create and maintain documentation projects and timelines
Perform Quality Assurance oversight of manufacturing and site activities
Ensure manufacturing compliance with cGMPs, applicable procedures, and batch records
Perform real-time review of manufacturing batch records, logbooks, and ancillary documents
Perform product label reconciliation for Manufacturing Operations
Perform GMP Walk-throughs of manufacturing and site areas
Write and approve deviations

Requirements

Bachelor's Degree preferred
Minimum of 3 years in Quality Assurance within a manufacturing GMP facility
1 year of direct experience with writing deviations and reviewing investigations

What We Offer

At Bristol Myers Squibb, we offer a competitive salary and benefits package, as well as opportunities for professional growth and development. We are committed to creating a diverse and inclusive work environment, where everyone has the opportunity to succeed. If you are a motivated and detail-oriented individual who is passionate about quality and patient safety, we encourage you to apply for this exciting opportunity.

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