Manager, Quality Operations Drug Product, QP Team job opportunity at Bristol Myers Squibb.

Home Jobs In Ireland Tag: Quality Operations Drug Product, QP Team Manager, Quality Operations Drug Product, QP Team position at Bristol Myers Squibb


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Bristol Myers Squibb Manager, Quality Operations Drug Product, QP Team
Experience: 3-years
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Quality Operations Drug Product, QP Team

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degreeAssociate
loacation Dublin - IE, Ireland
loacation Dublin - IE....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 . Bristol Myers Squibb Ireland Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units. Ireland is home to External manufacturing’s global headquarters, the business unit responsible for the management of manufacturing contract operations (CMO’s) and ensuring reliable supply of product to patients across the Bristol Myers Squibb global network. This includes management of, and working in conjunction with, third party contract manufacturers and internal manufacturing sites. In Ireland, External Manufacturing has two sites; Global Headquarters based in Dublin 15 and a distribution centre in Shannon, Co Clare. For more information about Bristol Myers Squibb, visit us at BMS.com/ie The Role BMS External Manufacturing is looking to recruit on a fixed term, 12 months contract, a Manager, Quality Operations Drug Product, QP Team, reporting to Senior Manager, QA Lead – Pharma QP Operations. This role is open for ExM Dublin Plaza office and Utrecht BMS office. Based on your function, department or individual position, you will have the opportunity to discuss with your Manager the option to work remotely up to 50% of the time, over a two-week period, with the flexibility to choose the days that align with your collaboration needs Key Duties and Responsibilities: Support the Qualified Person with the Batch Certification function Prepare and review of batch documentation packages for QP release as per SOP requirements Communicate and collaborate with BMS Supply Chain to support QP release schedule, as required Completeactivities associated with new product introductions Authoring, review and approval of QA-related procedures and relevant controlled documents. Provide training to new team members, as required Support the site inspection readiness program for corporate and regulatory inspections and act as SME, when required Preparation of quality documents supporting batch certification e.g., QP declarations, Product Quality Reviews and Risk Assessments Act as functional lead for QMS activities e.g., Change Control assessments, Investigations and Quality Agreement updates. Perform additional team tasks as agreed to support effective running of the function Support Opex programs and champion continuous quality improvement initiatives Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements. In addition to the BMS Core behaviours, the job holder should exhibit; Good interpersonal, oral, and written communications skills. The Manager must demonstrate an ability to prioritise objectives from multiple projects. Excellent communication and ability to contribute to team based in collaborative environment is essential. Proactive in resolving issues and escalating to management when necessary. Must lead by example in terms of displaying the BMS behaviours Qualifications, Knowledge and Skills Required: BSc in Science or related discipline with 2-3 years QA experience in a pharmaceutical environment, preferably Operations based. A clear understanding of cGMP requirements for manufacturing and/or systems and compliance Demonstrated proficiency communicating and collaborating at a variety of levels and across divisions Demonstrated ability to recognise issues, highlight risks and prioritise workload based on schedule requirements Proven success working well in a team environment with flexibility to react to changing business needs QP Eligible (Desirable) 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, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. BMSBL #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. R1595575 : Manager, Quality Operations Drug Product, QP Team

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