Scientist RSCR

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Support of pharmaceutical operational activities for the Reference Standard and Critical Reagent (RSCR) Group. Primary role will be to support project / product interaction and operational needs within the RSCR Operations group including ownership and facilitation of key aspects for biologics and small molecules focusing on external manufacturing and external vendors.

• BS or MS in biological sciences, chemistry, or related scientific disciplines
• Experience/Knowledge: 5 to 8 years of experience in the biotech or pharmaceutical industry
• General experience in Analytical techniques, Separation science, Chemical Analysis,
• Instrumentation and Method Validation and or bioanalytical techniques and biologics development.
• Industry experience in biotech/biologics, specifically working with reference standards and/or critical reagents is also desirable

• Manage RSCR portfolio inventory and scheduling to meet project deliverables and timelines.
• Maintain sustained communication with stakeholders and key partners regarding material supplies and deliverables.
• Assures that the physical inventory and inventory operations (i.e. receiving bulk material, subdividing material, labeling, storage, and disposition) are maintained and up-to-date.
• Address potential risks and operational issues by identifying, documenting, resolving, communicating or escalating to senior leadership when appropriate. Collaborate with key stakeholders to manage expectations.
• Interacts with the respective reference standard re-qualification process including developing test protocols, reviewing data, scheduling testing, calculating purity, and assigning expiration dates.
• Monitors key aspects of the business such as Statement of work (SOW), Purchase Orders (PO), inventory and burn rate analysis, and actively participate in investigations and providing documentation/filing support.
• Assists in training staff in proper handling, storage, subdivision and vialing of reference standard bulk materials, labeling, packaging and shipment as well as cGMP, and site Quality practices.
• Work well within diverse/inclusive high performance teams and maintain a strong relationship with operational and functional leadership.

Up to 5%

New Brunswick – NJ – US: $91,070 – $110,354 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience.

Final, individual compensation will be 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

• Health Coverage:
  Medical, pharmacy, dental, and vision care.
• Wellbeing Support:
  Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financia…