Specialist QC Material Management Analyst page is loaded
Specialist QC Material Management Analyst
Apply locations Cruiserath - IE time type Full time posted on Posted Yesterday job requisition id R1588654
Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
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.
Bristol Myers Squibb Ireland
Bristol Myers Squibb is a leading global biopharma company focused on discovering, developing and delivering innovative medicines for patients with serious diseases in areas including oncology, haematology, immunology, cardiovascular and neuroscience.
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.
Bristol-Myers Squibb is seeking to recruit a Specialist QC Material Management Analyst to join the QC Site Operations team at its Multi-Product Cell Culture Drug Substance Facility in Cruiserath, Dublin.
The Role
Reporting to the QC Material Management Supervisor, they will be responsible for supporting site activities related to performing testing of Raw Materials, in-process samples and laboratory duties in accordance with cGMP regulations.
Key Duties and Responsibilities:
* 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.
* Compliance with Standard Operating Procedures and Registered Specifications.
* Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
* Ensure all Drug Substance, Drug Product and Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.
* Manage TempTales and shipping documents when receiving samples from external sites.
* Log in 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 Lead, if any.
* Aliquot samples for the QC activities for Global Biologics Laboratory and Multi Product Cell Culture (MPCC) Facility.
* Performing QC testing (TOC, Nitrates, Conductivity) of water samples. Performing analysis of Raw Materials including HPLC, GC, KF, UV, IR and wet chemistry techniques.
* Batch paperwork review, and reconciliation of analysis performed in laboratory. Ensuring that any out of specification results are investigated according to site procedures.
* Assisting with out of specification investigations and deviations using the Infinity system.
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 related discipline along with at least 1 year of experience in a pharmaceutical / healthcare laboratory or related technical function.
What’s important to us
* 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.
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.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science”, every BMS employee plays an integral role in work that goes far beyond ordinary.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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