Overview
Working with Us
Bristol Myers Squibb offers a unique environment where challenging, meaningful work transforms patients' lives and career trajectories. From optimizing production lines to pioneering cell therapy breakthroughs, we provide opportunities uncommon in scope and scale, alongside high‑achieving teams.
We value balance and flexibility, providing competitive benefits and programs that support both professional and personal goals. Read more at careers.bms.com/working-with-us.
Bristol Myers Squibb Ireland
Operating in Ireland since 1964, BMS employs over 650 people across diverse units. Our state‑of‑the‑art biopharmaceutical manufacturing facility at the Cúirtach Biologics Campus in Dublin produces multiple therapies within the global supply network. The site has received industry awards and is recognized as a Great Place to Work.
The Role
Fixed‑term contract Manager, QC Sample Management reporting to the Senior Manager, Material Management.
Key Duties And Responsibilities
* Responsible for the sample management process for all QC activities for Global Biologics Laboratory and MPCC
* Management of the Retains Programs
* Ensure adherence to sample chain of custody in the Biologics Laboratory
* Lead and engage a materials management team, recruiting where necessary
* Coordinate sample shipments with internal and external stakeholders to support testing schedules, drug substance release, raw material release, and stability programs
* Manage investigations related to sample handling, receipt, long‑term storage, retains, and raw materials
* Oversee sample temperature tracking devices, shipping documentation, electronic and paper logbooks, and LIMs/CIMs data
* Ensure all sample management procedures comply with corporate and regulatory requirements
* Maintain safety standards during all laboratory activities
* Support raw material testing for batch approval, investigations, and recruitment
Qualifications, Knowledge and Skills Required
* B.Sc. in Biochemistry or related discipline with at least 5 years in a GMP laboratory setting and sample management experience
* Knowledge of routine biopharmaceutical drug product and drug substance laboratory best practices (desirable)
* Leadership ability, flexibility, strong communication, and teamwork skills—global communication required
* Experience with electronic systems such as LIMs/CIMs, Trackwise/Infinity, and SAP
* Experience in corporate and regulatory audits
Benefits
* Competitive salary and bonus structure
* Retirement plan contributions
* Family health insurance
* 27 days annual leave
* On‑site gym and life assurance
On‑Site Protocol
Occupancy type (site‑essential, site‑by‑design, field‑based, or remote‑by‑design) depends on role responsibilities. Site‑essential roles require 100 % on‑site shifts. Site‑by‑design roles may offer a hybrid model with at least 50 % on‑site presence. Field‑based and remote‑by‑design roles may require travel.
BMS supports reasonable accommodations for disabilities throughout the hiring process. For adjustments, contact adastaffingsupport@bms.com. Visit careers.bms.com/eeo‑accessibility for the full Equal Employment Opportunity statement.
Applicants may be considered with arrest and conviction records, per applicable laws. Vaccination requirements for COVID‑19 may apply. If you live or expect to work from Los Angeles County, review the required information at https://careers.bms.com/california‑residents/.
All personal data processed during the application will be handled per privacy laws and regulations.
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