Senior Specialist, Field Quality QA Operations Devens - MA - US R1603371

## Senior Specialist, Field Quality QA Operations Devens - MA - USFind out how well you match with this job
** Working with Us
** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:  position is critical to maintaining quality oversight and ensuring GMP compliance in day-to-day manufacturing operations.

The Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs, and supporting timely return-to-service (RTS) walkthroughs to confirm that manufacturing areas and equipment are properly cleaned, calibrated, and ready for production use.

The role also working closely with Manufacturing Operations to investigate and resolve manufacturing issues as they arise. Additionally, this position contributes to authoring and revising quality SOPs, supporting the review and closure of no-impact manufacturing deviations, and conducting proactive area inspections and readiness reviews to uphold both internal quality standards and external regulatory requirements.

This is a high-visibility, floor-based role that is integral to real-time quality assurance, batch release readiness, and audit preparedness. The absence of this resource creates increased risk for delayed batch review, reduced on-floor QA presence, gaps in RTS activities, and decreased support in deviation resolution.

Shift Available:  Monday - Friday, Onsite Afternoon Shift (2 p.m.

- 10:30 p.m.) Responsibilities:
* Quality floor support of complex manufacturing activities
* Performs manufacturing batch production record review in support of product release in accordance with specifications and SOPs.
* Perform walkthroughs of GMP areas documenting observations and areas of concern.
* Perform training on routine facility Quality tasks for new team members.
* Supports return to service walkthroughs and Manufacturing inspection readiness walkthroughs per procedures as needed.
* Assures all electronic and paper documentation, which requires QA review is in compliance with corporate and site procedures, cGMP regulations, and other industry guidelines.

Knowledge & Skill:  
* Knowledge of biotech bulk and finished product manufacturing, analytical testing is highly desirable.
* Knowledge of US and EU cGMP regulations and guidance.
* Knowledge of electronic or paper batch record systems, DeltaV, and other electronic systems applicable to laboratory test result generation, inventory management, investigations and equipment tracking and maintenance is desirable.
* Field Quality may have business needs to interact with any employee at any level of the Devens Facility with daily interactions with other Quality staff, Supply Chain, Digital Plant, Site Engineering and Manufacturing staff, as they conduct record reviews and respond to events occurring during day to day operations.
* Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.  Coordinates with higher level leads and/or supervisor on decisions and applies appropriate notification to management as appropriate.
* Receives assignments which require the application of a defined process to complete the assignment.  As such specific assignments are allocated based upon the recipient’s demonstrated capabilities with the…