Manager, Senior Manufacturing Support Scientist/Engineer

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. 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 Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company’s first European biologics manufacturing facility. This state-of-the-art facility will produce multiple therapies for the company’s growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug products for the network, is also based on the Cruiserath Biologics Campus. BMS Cruiserath has been awarded “Biopharma Company of the Year 2019” in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020 and 2021. For more information about Bristol Myers Squibb, visit us at BMS.com/ie The Role BMS Cruiserath Biologics is seeking to recruit a permanent Manager, Senior Manufacturing Support Scientist/Engineer reporting to the Associate Director the Projects team of the Manufacturing group. The Manager, Senior Manufacturing Support Scientist/Engineer role is a key contributor to a successful implementation of new products into manufacturing in the BMS network in Cruiserath, Dublin Key Duties and Responsibilities Manufacturing Support & Co-ordination with the introduction of new products and technical transfers into BMS Cruiserath. Identifying and developing manufacturing processes and associated documentation with the technical transfer of an NPI into BMS Cruiserath. Leading projects to completion. Lead, own and coordinate associated change controls to implement new products into Cruiserath. Providing SME input into cross-functional teams investigating & optimizing manufacturing processes, procedures and documentation to support NPI introduction. Supporting external and internal audits. Working with cross-functional teams on the introduction of new consumables and raw materials for the creation of the SAP master Bill of Materials. Working to implement a “Right-First Time Culture” and provide leadership in the use of Operational Excellence principles. Supporting the disposition process. Carrying out organizational activities such as purchasing & co-coordinating communication information when introducing a new NPI. Working closely with the shift teams to ensure that operations are run efficiently and effectively at all times during the implantation of a new product. This element of the job may require ad hoc shift support to support a business need. At times, there will be requirements to support manufacturing on shift or out of hours during the introduction of NPIs. Own & drive change controls, CAPA’s, investigations, improvement projects and operational safety. Minimizing human error and working with operations to remove sources of error. Departmental Approver of Operations procedures, electronic batch records and other GMP documentation and provide technical training and knowledge transfer to the Operations team during the technical transfer process Multiproduct and product changeover: implementing new product introductions from an Operations perspective. Developing strong working relationships with Quality, Engineering, Technical Services, Supply Chain, Regulatory Affairs, Human Resources and Finance. Leading and implementing new technology solutions such as Single-Use technology. Qualifications, Knowledge and Skills Required: Minimum a BSc degree in Science/Engineering or related subject and extensive biologics manufacturing or technical support experience (Mammalian Cell Culture processes experience). Ability to manage and coordinate technical projects and in-depth working knowledge of GMP biologics manufacturing equipment and process automation in a large- scale production facility. Demonstrated proficiency in communicating and collaborating at a variety of levels, coupled with excellent organization and planning skills. Proven success working in a team environment, as well as strong leadership & influencing skills, with the flexibility to react to changing business needs. Problem- solving and project management ability, as well as lean manufacturing experience. Proven ability to support the close-out of complex technical investigations. Strong working knowledge of systems such as Delta V, MES Syncade and SAP. Excellent presentation and communication skills. What’s important to us: Employees are expected to display the BMS Values, which move us toward our mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases: · Passion: Our dedication to learning and excellence helps us to deliver exceptional results. · Innovation: We pursue disruptive and bold solutions for patients. · Urgency: We move together with speed and quality because patients are waiting. · Accountability: We all own BMS’ success and strive to be transparent and deliver on our commitments. · Integrity: We demonstrate ethics, integrity and quality in everything we do for patients, customers and colleagues. · Inclusion: We embrace diversity and foster an environment where we can all work together at our full potential. We have a passion for tackling the toughest diseases, which inspires innovation and speed in our daily work and a sense of accountability to the patients we serve. 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, 23.5 days annual leave plus 3 Company days, life assurance, on-site gym and gain-sharing bonus. BMSBL Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 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.