Senior Specialist, Qc Materials Management, Incoming Components

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Bristol Myers Squibb Ireland 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 companys first European biologics manufacturing facility.
This state-of-the-art facility will produce multiple therapies for the companys growing biologics portfolio.
Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus.
BMS Cruiserath has been awarded Biopharma Company of the Year 2019 in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020 and 2021.
For more information about Bristol Myers Squibb, visit /ie The Role Cruiserath Biologics are seeking to recruit on a permanent contract, Senior Specialist, QC Materials Management with responsibilities for QC testing and support activities in the QC laboratory.
Reporting to the QC materials Manager, Incoming Components, the QC Senior Specialist provide support directly and indirectly to the QC laboratory.
NOTE: Shift work may be required as part of this role.
Key Duties and Responsibilities: Manage Operations Assisting with qualification of laboratory instruments.
Participate in regulatory audits as required.
Performing routine data analysis, assist in the investigation of OOS results, perform trending analysis and writing investigation reports and event reviews.
Execute and assist in technical transfer and co-validation activities.
Perform instrument performance checks and calibration.
Participate in troubleshooting complex testing and instrumentation issues.
Testing of materials/components to meet attainment and release metrics.
Manage Information Assisting in updating and issuing documentation, including SOPs, as required.
Accurately documenting laboratory work and instruct any less experienced analysts on the best documentation practices.
Complete peer review of documented lab results, logbooks, and associated documents to ensure testing has been completed in compliance with procedures.
Safety Prioritise safety in every aspect of the role.
Lead by example in exemplifying safety behaviours Teamwork Participate in cross functional teams.
Provide support to other departments to ensure qualification and production schedules are adhered to.
Development Coach analysts within the group.
Training of laboratory personnel and scheduling of training where required.
Housekeeping Maintain lab to highest standards to ensure all assigned areas are maintained by designees.
Perform all other activities as indicated by Supervisor.
Designee Responsibilities Can act as a designee for the Manager, QC Materials Management, for the following task: May sign documentation on behalf of other Material Management Analyst.
May have other Material Management Analyst, Technical Leads, Managers and Supervisors sign documentation on behalf of the Raw Material Analyst.
May be assigned by Supervisors, Managers, and other Senior Analysts to sign documents on their behalf.
Complete work scheduling as a designee for the Supervisor Support all required laboratory and laboratory support activities as directed by QC Materials Management.
Qualifications, Knowledge and Skills Required: In addition to the BMS Core behaviors, the job holder should exhibit.
Good interpersonal, oral, and written communications skills.
Technical expertise should include among the following: Incoming Component testing, FTIR, UV, Appearance.
The Senior Analyst must demonstrate an ability to coach and mentor others, as well as be able to prioritize objectives from multiple projects.
Excellent communication and ability to contribute to and lead team based in collaborative environment is essential.
Proactive in resolving issues and escalating to management when necessary.
Must lead by example in terms of displaying the BMS behaviors, passion, accountability, innovation, and speed.
BS degree in scientific area with a minimum of 5 years experience in the (bio) pharmaceutical industry.
The QC Senior Analyst Materials Management, Incoming Component Senior Specialist should hold a minimum of a BSc.
in science or related discipline.
5 years pharmaceutical testing experience is preferable but not a requirement.
Experience in working as part of a team, project management and activity scheduling.
Experience in personnel management is preferable but not required.
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.
Youll 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.
BMSBL #LI-Onsite If you come across a role that intrigues you but doesnt perfectly line up with your resume, we encourage you to apply anyway.
You could be one step away from work that will transform your life and career.
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.
Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol BMS has a diverse occupancy structure that determines where an employee is required to conduct their work.
This structure includes site-essential, site-by-design, field-based and remote-by-design jobs.
The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility.
Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility.
For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture.
For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.
Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.
If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to.
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BMS cares about your well-being and the well-being of our staff, customers, patients, and communities.
As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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Skills: equipment qualification QC laboratory experience component testing experience