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Scientist/Senior Scientist/Principal Scientist, Exploratory Biopharmaceutics


Bristol Myers Squibb


Location

Jersey | United Kingdom


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. Read more: careers.bms.com/working-with-us .

Position Summary

Within Exploratory Biopharmaceutics at BMS, you will have the unique opportunity to profoundly affect patients' lives. Join our multidisciplinary research teams in developing innovative, effective, and safe therapeutic molecules. We're seeking a Scientist, Senior Scientist or Principal Scientist eager to shape the future in our dynamic early development team. The role involves creating biopharmaceutics and formulation strategies that align with therapeutic exposure goals for active clinical and preclinical studies.
  • Engage in a cooperative Pharmaceutical Development setting, liaising across departments and therapeutic domains.
  • Implement biopharmaceutics, ADME, DMPK, modeling, and chemistry principles and technologies to establish effective and robust products.
  • Pinpoint key biopharmaceutics performance attributes and potential risks vital for formulation design, ensuring smooth clinical progression.
  • Independently manage development projects, interfacing with diverse functional groups such as Clinical Pharmacology, Discovery, Toxicology, and Regulatory teams.
  • Compile comprehensive biopharmaceutics packages for regulatory submissions.

Job Requirements/Qualifications for each level
  • Principal Scientist
  • Ph.D. in Pharmaceutics, Pharmacokinetics, or a related scientific discipline, coupled with 4-8 years of pertinent experience.
  • Robust comprehension of ADME, PK, and PK-PD principles. Demonstrated analytical and problem-solving acumen is indispensable.
  • Familiarity with cutting-edge academic and industrial applications in biopharmaceutics, pharmacokinetics, and ADME principles.
  • An established track record of expertise, evidenced by publications and presentations.
  • A fervent drive for innovation and a propensity to operate with an entrepreneurial spirit in a matrix structure.
  • Effective collaboration and stellar interpersonal abilities are essential. This includes engaging with and influencing a vast spectrum of both internal and external stakeholders across organizational tiers.
  • Hands-on modeling proficiency, encompassing PBPK, PD, popPK, QSP, etc., will be considered a distinct advantage.
  • This role demands innovation. The ideal candidate will be highly organized, possess outstanding communication and critical thinking abilities, and thrive in a collaborative and idea-centric environment.

  • Senior Scientist
  • Ph.D. in Pharmaceutics, Pharmacokinetics, or a related scientific discipline, coupled with 2-4 years of pertinent experience.
  • Hands on experience with in vitro testing, PBPK modeling, or DMPK/ADME principles, is expected in this lab-based role.
  • Experience applying in vivo, in vitro, and in silico solutions to biopharmaceutics studies and interpret data to inform preclinical risk assessment of assets in the pipeline
  • Write and review study reports/research articles/patent applications and other documents as needed.
  • Familiarity with cutting-edge academic and industrial applications in biopharmaceutics, pharmacokinetics, and ADME principles.
  • A fervent drive for innovation and a propensity to operate with an entrepreneurial spirit in a matrix structure.
  • Effective collaboration and stellar interpersonal abilities are essential. This includes engaging with and influencing a vast spectrum of both internal and external stakeholders across organizational tiers.
  • This role demands innovation. The ideal candidate will be highly organized, possess outstanding communication and critical thinking abilities, and thrive in a collaborative and idea-centric environment.

  • Scientist
  • Ph.D. in Pharmaceutics, Pharmacokinetics, or a related scientific discipline, coupled with 0-2 years of pertinent experience.
  • Hands on experience with in vitro testing, PBPK modeling, or DMPK/ADME principles, is desirable in this lab-based role.
  • Creatively apply in vivo, in vitro, and in silico solutions to biopharmaceutics studies and interpret data to inform preclinical risk assessment of assets in the pipeline
  • Write and review study reports/research articles/patent applications and other documents as needed.
  • A fervent drive for innovation and a propensity to operate with an entrepreneurial spirit in a matrix structure.
  • Effective collaboration and stellar interpersonal abilities are essential. This includes engaging with and influencing a vast spectrum of both internal and external stakeholders across organizational tiers.
  • This role demands innovation. The ideal candidate will be highly organized, possess outstanding communication and critical thinking abilities, and thrive in a collaborative and idea-centric environment.

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 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
Physical 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 [email protected] . 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.


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