Specialist, QC Sample Management

Bristol Myers Squibb; Fingal; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Annual bonus

Pension contribution

Family health insurance

27 days annual leave

On-site gym

Life assurance

Job summary

Bristol Myers Squibb is seeking a Specialist, QC Sample Management to support sample processing across Drug Substance, Drug Product, and stability workflows at Cruiserath. You will manage sample logging, storage, release for QC testing, and ensure GMP-compliant operations in a fast-paced biotech environment.

The role offers growth, comprehensive benefits, and a collaborative culture that prioritizes patient outcomes, inclusion, and continuous improvement.

Responsibilities

• Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.
• Ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe.
• Liaise with Warehouse Cryogenics Logistics (WCL) to ensure all Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.
• Support the implementation and execution of Drug Product Stability at Cruiserath
• Manage TempTales and shipping documents when receiving samples from external sites.
• Logging of samples to LIMS/CIMS or logbooks, and label accordingly.
• Release samples for QC testing.
• Storage of backups and reserve samples.
• Perform monthly reconciliation and report deviations to Sample Management Manager, if any.
• Reconstitute and Aliquot samples for the QC activities for Global Biologics Laboratory, Global Stability and Multi Product Cell Culture (MPCC) Facility.
• Support buffer preparation for the QC Separations lab
• Support enrolment of bulk Drug Product Stability Study Samples
• Support timepoint pulls of Drug Product Stability Study Samples
• Generate and update SOPs and other relevant documents as required.
• Maintain a high standard of GMP compliance including the completion and provision of training as required.
• Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
• Support continuous improvement initiatives across the department and within the team
• Performing any other activities as indicated by the Lab Manager.

Job description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Key Responsibilities

• Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.

• Ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe.

• Liaise with Warehouse Cryogenics Logistics (WCL) to ensure all Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.

• Support the implementation and execution of Drug Product Stability at Cruiserath

• Manage TempTales and shipping documents when receiving samples from external sites.

• Logging of samples to LIMS/CIMS or logbooks, and label accordingly.

• Release samples for QC testing.

• Storage of backups and reserve samples.

• Perform monthly reconciliation and report deviations to Sample Management Manager, if any.

• Reconstitute and Aliquot samples for the QC activities for Global Biologics Laboratory, Global Stability and Multi Product Cell Culture (MPCC) Facility.

• Support buffer preparation for the QC Separations lab

• Support enrolment of bulk Drug Product Stability Study Samples

• Support timepoint pulls of Drug Product Stability Study Samples

• Generate and update SOPs and other relevant documents as required.

• Maintain a high standard of GMP compliance including the completion and provision of training as required.

• Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.

• Support continuous improvement initiatives across the department and within the team

• Performing any other activities as indicated by the Lab Manager.

Why you should apply

• You will help patients in their fight against serious diseases
• You willbe part ofa 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.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: 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/

For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

Data Protection

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Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1607986 : Specialist, QC Sample Management