Manager, QC Technical Lead Raw Materials

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 product 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 Manager, QC Technical Lead Raw Materials for an 18-month contract, reporting to the Senior Manager, QC Materials in the QC Site Operations team, the Technical Lead will provide technical expertise and oversight to the QC Raw Materials Testing group. Key Duties and Responsibilities: Develop and maintain the Raw Materials Testing Programs, support testing activities, ensuring compliance with regulatory and corporate directives for the QC Raw Materials laboratory that support the Multi Product Cell Culture (MPCC) DS facility and play a key role in the technical transfer and validations of new materials and methods at Cruiserath. Provide technical leadership and guidance to the QC Site Operations team on the establishment of the laboratory procedures and practices, quality system elements, equipment qualifications, and cross-functional Raw Material Testing support for the MPCC/Warehouse facility. Participate in regulatory audits as the Raw Material Testing SME Participate in laboratory investigations to ensure timely close-out Directly involved in managing the technical transfer and validation of new materials Establish communication channels between all stakeholders to ensure visibility on end-to-end process. Participate in cross-functional teams to support Raw Material and Batch release. Participate in definition and establishment of the laboratory Quality Systems and Operational processes Participate in troubleshooting complex laboratory testing issues Qualifications, Knowledge and Skills Required: The ideal candidate should hold a minimum of a BSc. in Chemistry or related discipline and must have at least 5 years hands on experience in a Biopharmaceutical setting. Technical expertise: HPLC, GC, FTIR, UV, TOC, RAMAN and general Raw Material laboratory techniques. Experience with laboratory data systems, Empower, Tiamo, LIMS and CIMS would be an advantage. The successful candidate must demonstrate a problem solving ability, as well as the ability to prioritise objectives from multiple projects. Excellent communication and the ability to contribute to and lead in a team based collaborative environment is essential. Experience in technical transfer and validation of chemical methods as well as cleaning method validation. Proven track record of delivery 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
LI-Hybrid 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.