Senior Specialist, QC Quality Systems
Bristol Myers SquibbIreland
Posted April 2, 2026
Contract / Temporary
About the Company
At Bristol Myers Squibb, we work every day to transform patients’ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers you’ll experience. Join us and pursue innovative ideas alongside some of the brightest minds in biopharma, collaborating with a team rich in diversity of experiences, and perspectives. We have built a sustainable pipeline of potential therapies and are leveraging translational medicine and data analytics to understand how we can deliver the right medicine to the right patient, at the right time, to achieve the best outcome. Whether in a scientific, business or supporting function, a career at BMS means you’ll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, you’ll be on the cutting edge of powerful innovation in oncology, hematology, immunology, cardiovascular disease, and fibrosis, with colleagues united in the mission to help patients. Through the Bristol Myers Squibb Foundation, we also promote health equity and seek to improve health outcomes of populations disproportionately affected by serious diseases and conditions. Our mission is to give new hope to help patients prevail over serious disease – it drives everything we do. Review our Social Media Community Guidelines at: https://www.bms.com/social-media-community-guidelines.html
Job Description
Bristol Myers Squibb is seeking a Senior Specialist, QC Quality Systems to lead and manage QC Investigations and Change Controls in a FIXED TERM contract. The role requires proficiency in communication and collaboration, problem solving, and project management.
Requirements
- Proficiency in communication and collaboration at a variety of levels
- Proven success working well in a team environment with flexibility to react to changing business needs
- Demonstrated problem solving, project management ability
- Excellent time management and organizational skills
- Excellent technical writing skills
- Previous investigations experience is an asset
- Ability to research and have an excellent understanding of new areas/tasks/assays under investigation promptly
- Education minimum of a B.Sc. Biochemistry or related discipline
- At least 3 years’ experience, in a GMP laboratory setting ideally within a biologics laboratory
- A minimum of 1 years’ experience with demonstrated effectiveness using quality systems (investigations/change controls – Trackwise/Infinity) in a FDA and EMA regulated environment
- Knowledge of biologics QC testing (Separations, Bioanalytical, Microbiology, Raw Materials and Stability testing) is desirable
Benefits
- annual bonus
- pension contribution
- family medical assurance
- 27 day annual leave
- life assurance
- on-site gym