Bristol Myers Squibbother related Employment listings - Sayreville, NJ at Geebo

Bristol Myers Squibb

Working with UsChallenging.
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.
Read more:
careers.
bms.
com/working-with-us.
Scientist/Principal Scientist, Drug Product Development StatisticianBristol-Myers Squibb is seeking a Statistician to join the Integrated Technologies and Engineering group within the Drug Product Development function.
Are you looking for a patient-centric company that will inspire you and support your career? Then join our diverse and innovative team, where we provide rigorous statistical and data science solutions to a wide array of assignments, ranging from development to commercial manufacturing support.
Location:
New Brunswick, NJ, Summit, NJPOSITION ACCOUNTABILITIES:
Uses knowledge and expertise of statistics to collaborate with scientists in application of statistics to Drug Product Development:
Quality by Design, formulation development and optimization, process design and optimization, experimental manufacturing campaigns, determining manufacturing design spaces, validation and development of analytical assays, experimental and registrational stability studies, probabilistic assessment of risk for critical quality attributes.
The successful candidate contributes to the Chemistry, Manufacturing and Controls (CMC) aspects of biological and oral solid drug products.
Analyzes experimental data to support the development of product specifications and regulatory filings.
Engages in scientific and technical discussions with multi-disciplinary team members to move forward with speed and accountability.
Clearly communicates and documents results to stakeholders with diverse backgrounds, including non-technical audiences.
Develops visualization techniques to facilitate interpretation of experimental data and models by non-statisticians.
Trains scientists in data analysis, statistics, and visualization.
Applies regulatory guidelines to work and keeps abreast of technical and regulatory advancements.
Authors source documents used in CMC registrational filings.
Assists in developing responses to health agencies.
Participates in functional and cross-functional initiatives, including process and quality improvements.
Skills/knowledge required for ScientistPhD in Statistics, Biostatistics, or a related field with 0-2 years of experience or MS with 2 - 6 years of relevant industry experience.
Candidates with documented equivalent experience in an applied statistical setting will be considered.
Intermediate/advanced knowledge of Design of Experiments (DoE) for nonclinical applications, multivariate statistics, Bayesian statistics, and mixed models is essential.
Experience with R or Python, SAS, JMP is desired.
Understanding of regulatory guidelines (e.
g.
cGMP and ICH guidance) that impact the use of statistical analysis is desired.
A successful candidate will have excellent computational, written and verbal communication skills, strong organizational abilities and an ability to work with a diverse group of scientists and engineers.
Embrace BMS shared values of passion, innovation, urgency, accountability, inclusion and integrity.
Skills/knowledge required for a Sr.
Scientist/Principal ScientistPhD in Statistics, Biostatistics, or a related field with 2-6 years of experience or MS with 4 - 9 years of relevant industry experience.
Candidates with documented equivalent experience in an applied statistical setting will be considered.
Advanced knowledge of Design of Experiments (DoE) for nonclinical applications, multivariate statistics, Bayesian statistics, and mixed models is essential.
Experience with R or Python, SAS, JMP is essential.
Understanding of regulatory guidelines (e.
g.
cGMP and ICH guidance) that impact the use of statistical analysis is preferred.
A successful candidate will have excellent computational, written and verbal communication skills, strong organizational abilities and an ability to work with a diverse group of scientists and engineers.
Pharmaceutical development experience and knowledge of nonclinical/ CMC statistics is desired.
Expertise in other scientific/engineering/computing areas is a plus.
Embrace BMS shared values of passion, innovation, urgency, accountability, inclusion and integrity.
#LI-HybridIf 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 CareersWith a single vision as inspiring as Transforming patients' lives through science(TM) , 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 adastaffingsupport@bms.
com.
Visit careers.
bms.
com/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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
About the Company:
Bristol Myers Squibb.
Estimated Salary: $20 to $28 per hour based on qualifications.

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