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Senior Scientist, Method Development (Regulated Bioanalytical Laboratory)

Company: Disability Solutions
Location: Princeton
Posted on: March 30, 2024

Job 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: Summary--The position will be responsible for evaluating and de-risking methods from discovery to development stage. The individual will provide leadership on the method development and non-regulated study support of development compounds from various modalities (small molecule, large molecule therapeutics, etc.) via tandem/high resolution mass spectrometry. In addition, the candidate will play a critical role as an expert in the evaluation advanced laboratory equipment. There are also development opportunities to act as a BA lead on cross-functional study teams, and work with them to address bioanalytical-related issues.------Key Responsibilities--

  • Evaluate and apply novel techniques or approaches to address challenging bioanalytical issues.--
  • Conduct in-house bioanalytical support for exploratory/development programs with tandem/high resolution mass spectrometry-based method development, method troubleshooting, sample analysis, data interpretation, to report preparation.--
  • Be the technical expert on extraction, chromatography, mass spectrometric instrumentation, stability, and other method related issues.----
  • Interact with bioanalytical CROs to address method related issues and provide leadership for the knowledge transfer of novel technologies.--
  • Keep management apprised of project status and current scientific trends using written and oral summaries, as well as presentations.--Basic Qualifications:
    • Bachelor's Degree
      • 7+ years of academic and / or industry experienceOr
        • Master's Degree
          • 5+ years of academic and / or industry experienceOr
            • Ph.D. or equivalent advanced degree in the Life Sciences
              • 2+ of academic and / or industry experiencePreferred Qualifications
                • Ph.D. or equivalent advanced degree in the Life Sciences and 2+ of academic and / or industry experience
                • Preferred candidate will have a degree in chemistry, biochemistry, biology or related fields, plus relevant drug development experience at either a pharmaceutical company or a bioanalytical CRO.
                • A good understanding of bioanalysis and its role in drug development, including method development, validation, study support, and impact of quality bioanalytical data to PK/PD correlation.
                • Strong LC-MS/MS and LC-HRMS skills with separation and quantitation (or identification) of small (e.g. chiral assay) or large molecule therapeutics (e.g. hybrid assays for ADC and PTM) and biomarkers (e.g. small molecule/protein assays) in biological matrices. A strong foundation and experience in using, maintaining, and trouble-shooting mass spectrometers is preferred.
                • A proven track record of method development accomplishments in the field (thru presentations or publications).
                • Good communication skills and experience in authoring and reviewing bioanalytical assay, troubleshooting assay issues and direct junior scientist.
                • Experiences in performing LC-MS/MS and LBA method development, qualification (or validation) and study sample analysis in a regulated environment.
                • Ability to multi-task and work in a collaborative team environment.
                • Ability to communicate effectively in a team-based environment.#LI - OnsiteIf 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 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. 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 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.

Keywords: Disability Solutions, Trenton , Senior Scientist, Method Development (Regulated Bioanalytical Laboratory), Healthcare , Princeton, New Jersey

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