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. 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. Read more .
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 company's first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the company's 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 us at
The Role
BMS Cruiserath Biologics is seeking to recruit a
Permanent
Senior Specialist, QC Quality Systems (Lead Investigator)
, reporting to the QC Quality Systems Team Lead. The QC Quality Systems Specialist will be part of a team who are responsible for supporting the Quality Control team with Investigations and Change Controls
Key Duties And Responsibilities
* Lead and manage QC Investigations assigned
* Facilitate root cause analysis and problem solving sessions
* Complete the generation of associated investigation reports
* Determine and create CAPA's, Effectiveness Reviews, and Supplemental Tasks as required
* Present investigations at IRB to senior management
* Leading and coordinating the initiation, implementation, and closure of QC Change Controls
* Ensuring the timely completion of all activities related to these quality systems
* Collation of metrics/KPI's and generation of associated dashboard read-out
* Communication with BMS local and global stakeholders
* Lead huddles, meetings, conference calls and provide read-outs
* Participate in the OpEx strategy and support process improvements
* Participate in internal and external audits
* Support additional QC analytical services activities, as required
Qualifications, Knowledge and Skills Required
* Proficiency in communication and collaboration at a variety of levels
* Proven success working well in a team environment with flexibility to react to changing business needs
* Demonstrated problem solving, project management ability
* Excellent time management and organizational skills
* Excellent technical writing skils
* Previous investigations experience is an asset
* Ability to research and have an excellent understanding of new areas/tasks/assays under investigation promptly
* Education minimum of a B.Sc. Biochemistry or related discipline
* At least 3 years' experience, in a GMP laboratory setting ideally within a biologics laboratory
* A minimum of 1 years' experience with demonstrated effectiveness using quality systems (investigations/change controls - Trackwise/Infinity) in a FDA and EMA regulated environment
* Knowledge of biologics QC testing (Separations, Bioanalytical, Microbiology or Raw Materials) is desirable
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 including an annual bonus, pension contribution, family medical assurance, 27 day annual leave, life assurance and on-site gym
If you come across a role that intrigues you but doesn't 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 a supportive culture, promoting global participation 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 an 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. Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.
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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