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Specialist, qc material management

Bristol Myers Squibb UK & Ireland
Manager
€60,000 - €80,000 a year
Posted: 10h ago
Offer description

Role Overview

Bristol-Myers Squibb is seeking to recruit a permanent contract Specialist, QC Material Management Analyst to join the QC Site Operations team at its Multi-Product Cell Culture Drug Substance Facility in Cruiserath, Dublin. Reporting to the QC Material Management Supervisor, the incumbent will support site activities related to performing testing of raw materials, in-process samples and laboratory duties in accordance with cGMP regulations.


Key Duties and Responsibilities

* Perform QC testing (TOC, nitrates, conductivity) of water samples, and analyse raw materials using HPLC, GC, KF, UV, IR and wet chemistry techniques.
* Complete laboratory documentation promptly and accurately as directed by the QC Material Management Supervisor.
* Receive test and reserve samples, critical reagents and standards; support sample shipments as required.
* Conduct routine data and trending analysis, investigate out‑of‑specification (OOS) or out‑of‑trend (OOT) results, and draft investigation reports and event reviews.
* Maintain a high standard of GMP compliance with Standard Operating Procedures and Registered Specifications, including providing required training.
* Assist in authoring and reviewing documentation, including SOPs.
* Review batch paperwork and reconcile analytical results; investigate any out‑of‑specification results per site procedures.
* Participate in internal and external inspections.
* Assist in technical transfers and material qualification work.
* Perform any other activities as indicated by the Lab Supervisor.


Qualifications, Knowledge and Skills Required

The successful candidate must demonstrate excellent written and verbal communication skills and the ability to work in a team‑based collaborative environment. The ideal candidate should hold a minimum of a third level qualification (degree) in Chemistry, Biology or a related discipline, along with at least one year of experience in a pharmaceutical or healthcare laboratory or related technical function.


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 receive a competitive salary and a comprehensive 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.

We encourage you to apply even if your resume doesn’t perfectly align with the role. You could be one step away from work that will transform your life and career.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. 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/. BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities, and recommends that all employees be fully vaccinated for Covid‑19 and keep up to date with Covid‑19 boosters.

Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

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