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Principal Scientist - Princeton, NJ, United States - Bristol-Myers Squibb
Description
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:
Bristol-Myers Squibb CompanyPosition:
Principal Scientist (ref.# 7801)
Location: 3551 Lawrenceville Road, Princeton, NJ 08540Duties: Use knowledge of or experience with: Bioanalytical Method Validation and Study Sample Analysis guidelines for biotherapeutic and small molecules, with regulatory expectations for bioanalytical method validations and study conduct to work on the method validation and implementation of ligand binding assays and LC-MS/MS (liquid chromatography–mass spectrometry/mass spectrometry) assays for the analysis of nonclinical and clinical pharmacokinetic, immunogenicity, and biomarker samples in discovery and regulated environments.
Analyze samples applying qualified and validated methods to support drug discovery and development programs using novel technologies to enhance assay quality and throughput.
Represent the department on inter-departmental teams and/or external partner meetings as the bioanalytical expert.Contribute to the preparation and author method reports, assay validation reports, bioanalytical study reports, bioanalytical sections to clinical study reports, and Standard Operating Procedures utilizing department templates.
Participate in the preparation of bioanalytical sections to regulatory filings and bioanalytical responses to regulatory filings. Process bioanalytical study samples using validated methods within Watson LIMS. Report study sample results to stakeholders. Troubleshoot ligand-binding assays and Tecan automation software when problems arise. Ensure that electronic laboratory notebook documentation is up-to-date as per departmental and Good Laboratory Practice guidelines. Ensure timely communication of abnormal laboratory observations to key stakeholders and management.Serve as instrument owner for the Gyrolab platform, laboratory owner of regulated laboratories, and subject matter expert for the department instruments and associated software.
Comply with applicable company and departmental Standard Operating Procedures, health authority guidance documents (i.e., ICH M10), Good Laboratory Practices, and company safety procedures.
Contribute to and lead Computer System Validations for regulated laboratory instrumentation. Serve as a subject matter expert for department Data Integrity and Compliance initiatives.Respond to internal and external audit reports and findings for sample analysis and method validations supported within the ligand-binding assay internal laboratory.
Prepare and present scientific material at internal and external meetings and contribute to scientific publications. The position supervises work of two (2) employees in the positions of Associate Research Scientist, Senior Scientist.Requirements:
Bachelor's degree (or foreign equivalent) in Pharmacology/Toxicology, Biochemistry, Chemistry, Biology or a related field plus 5 years of post-baccalaureate experience reflecting demonstrable ability in the skill set described above.
This position is eligible for our employee referral program.
Contact:
Althea Wilson Bristol-Myers Squibb Company 4931 George Road Tampa, FL starting compensation for this job is a range from $129,058 to $174,608, plus incentive cash and stock opportunities (based on eligibility).
The starting pay takes into account characteristics of the job, such as required skills and where the job is performed.
Final, individual compensation is decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Career Site.Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following:
Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K).
Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support.
Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility.
Parental, caregiver, bereavement, and military leave.Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources.
Other perks like tuition reimbursement and a recognition program.If BMS Careers Site link is not copy and pasting correctly, please add manually using the following address:
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 CareersWith 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 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 Visit 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.
