Manager Quality Systems, Investigations and CAPA - Devens, MA bei Bristol Myers Squibb BMS

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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. 
Position Summary

The Manager, Quality Systems is responsible for supporting the ownership and oversight of Devens Cell Therapy quality systems, such as CAPA, Investigations per established local and global standards. This position supports the overall compliance and performance of Devens Cell Therapy Quality Systems Management as it applies to the site level, including periodic assessments of process performance and continuous improvement opportunities

Duties/Responsibilities 

Review and approve complex site quality system deliverables and risk assessments associated with all aspects of manufacturing process including incoming, manufacturing, laboratory, facility, and utility systems.
Ensure quality system deliverables are robust and adequately address requirements and risks, by providing oversight and rubric reviews, as applicable.
Support the administration and maintenance of quality systems such as CAPA, Investigations, including metrics reporting and analysis, stakeholder communication, and governance meeting facilitation, as needed.
Share data/ knowledge within and across site and network. Build & maintain strong relationships with partner functions.
Lead meetings and represent function at cross functional and network meetings.
Identify improvement opportunities and drive team continuous improvement goals and projects.
Support internal and external inspections.
May act as subject matter expert and present quality system program overviews and related topics during audits.
Maintain compliance with assigned learning plan. 
Support integration of newer team members and provide guidance and coaching to users of the electronic QMS, CAPA, and Investigations quality systems, as required.
Lead meetings and represent function at cross functional meetings. Share data/ knowledge within and across teams. Build & maintain strong relationships with partner functions.
Reporting Relationship

This position is within the Devens Cell Therapy Compliance and Quality Systems Organization, reporting to the Director of Compliance and Quality Systems Management