Manager, QA Systems job opportunity at Bristol Myers Squibb.

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Bristol Myers Squibb Manager, QA Systems
Experience: 4-years
Pattern: full-time
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QA Systems

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degreeAssociate
loacation Cruiserath - IE, Ireland
loacation Cruiserath - I..........Ireland

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 . The Role BMS Cruiserath Biologics is seeking to recruit a permanent Manager, QA Systems . Reporting to the Senior Manager, QA Systems, the successful candidate will be responsible for the execution and performance of one or more quality systems at the Cruiserath site. Key Duties and Responsibilities: Develop and maintain quality systems at the Cruiserath site. Act as a Local Process Owner (LPO) for 1 or more quality systems (which may include, but is not limited to, any of: documentation, change control, annual product quality reviews, Corrective Action/Preventive Action, deviation monitoring, etc.) As LPO, be the local point of contact for the system(s) of responsibility. Oversee quality system performance and lead continuous improvement projects relating to the system(s) of responsibility. Provide cross-departmental support to ensure compliance with company policies, GMP and regulatory requirements. Participate in LPO and Community of Practice (COP) groups for relevant systems to ensure best practices are implemented at Cruiserath. Participate as an SME in self-inspection, Health Authority, Corporate or Customer inspections. Support audit readiness activities and act as a key member of the audit support team during inspections. Represent QA as a team member or project lead in operational excellence and cross-functional process improvement teams. Support the authoring, review and approval of site procedures. Support the completion of investigation/CAPA activities as required. Support the implementation of applicable global systems. Support the implementation or management of additional QA Systems as required.   Qualifications, Knowledge and Skills Required: The successful candidate will hold a BSc in science, engineering or a related discipline, along with 4+ years’ Quality experience in a biopharmaceutical environment. Thorough understanding of cGMP requirements for Quality Systems and Compliance. Excellent interpersonal skills are required, as is the ability to communicate well, both verbally and written. Ability to contribute to a team-based, collaborative environment promoting clarity of purpose and high commitment to business goals. Ability to prioritise objectives for multiple projects, adhere to schedule timelines while maintaining flexibility and attention to detail. Ability to participate in large and complex projects, develop schedules and provide effective communications to customer and stakeholders. Ability to network globally with the BMS network and stay current with the latest initiatives. Good troubleshooting skills and a flexible approach to objective management. Experience in regulatory inspections. Why you should apply You will help patients in their fight against serious diseases You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees. You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym #LI-Hybrid If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:  https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1597993 : Manager, QA Systems

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