Job Description
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 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.
Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus.
This position is responsible for providing statistical analysis, direction, and training to service clients in Global Product Development & Supply (GPS).
Major Duties and Responsibilities:
- Builds and fosters relationships with customers, stakeholders, and support groups globally to understand their statistical needs and determines sound statistical techniques for use.
- Collaborates with process analytical teams and subject matter experts in Manufacturing and Manufacturing Sciences & Technology to design studies and analyze complex datasets for process robustness and improvement.
- Supports analytical teams in QC and Analytical Sciences & Technology for method performance monitoring and reference standard qualification.
- Develops and selects appropriate statistical methods for the design and analysis of studies and programs to assure batch compliance and prevent rejections, reworks, complaints, and product recalls on a worldwide basis.
- Conducts thorough and careful analysis of data, gathers critical information, and provides appropriate recommendations and solutions based on corresponding statistical analyses and business needs.
- Demonstrates strong statistical skills while thinking in a clear, decisive manner. Reaches independent, logical solutions.
- Represents Global Statistics at product development, product protocol, and management meetings.
- Contributes to the globalization, improvement and standardization of processes, procedures, and systems in relation to Statistics while maintaining flexibility where required.
- Furthers the statistical awareness and statistical process control competency of other BMS personnel; participates in their training and development, as required.
- Acts as departmental interface with Information Technology on system-related projects. Performs programming (e.g., SAS) as needed.
- Creates, communicates, and supports the highest commitment to quality and compliance.
Education:
Ph.
D. in Statistics, Data Analytics, or Engineering with significant academic training in Statistics.
Proficiency in major statistical software packages (e.g., SAS, R, MINITAB, and JMP).
Experience / Knowledge Desired:
- Ability to work with a wide range of technically and culturally diverse individuals.
- Ability to analyze and interpret scenarios, and through effective study design and statistical analysis provide answers and appropriate courses of action.
- Knowledge of FDA/EMEA cGMPs and knowledge of other global regulatory compliance guidelines (e.g. ICH) for drug manufacturing, packaging and distribution.
- Able to work independently under limited supervision or as a team member to meet goals, objectives, and commitments.
- Proficient in writing formal reports, articles for publication and/or technical presentations.
- Demonstrates ability to effectively communicate technical information in an understandable, rational, and concise manner.
- Ability to integrate statistical and quality control concepts.
- Strong background in the chemical or biological sciences to facilitate a subjective understanding of the problems at hand.
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 days 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.
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 ProtocolBMS 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.
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.