Specialist,QualitySystems

**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: [careers.bms.com/working-with-us](https://careers.bms.com/working-with-us). **The Role** BMS Cruiserath Biologics is seeking to recruit a**Specialist, Quality Systems** on a fixed -term contract. **Specialist, Quality Systems** will join the QA Systems team and, along with other team members, will act as a key point of contact and provide cross-departmental support for a variety of document management systems and processes at the BMS Cruiserath site. Note: this role is based **on-site** due to the nature of the responsibilities. **Key Duties and Responsibilities:** * Preparation and issuance of controlled documentation to support manufacturing and testing activities * User support and maintenance of the electronic Document Management System (Veeva Vault) * Management of the Document Archive and Record Retention Systems * Maintenance of other document systems and processes e.g. SharePoint, Periodic Review tracking. * Delivery of GMP/GDP training * Participation in the internal and external audit program * Collection of quality metric data * Support completion of investigation/CAPA activities as appl