Scientist RSCR

Bristol Myers Squibb • New Brunswick, NJ

17d • Onsite

About The Position

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.

Requirements

• BS or MS in biological sciences, chemistry, or related scientific disciplines
• 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

Responsibilities

• 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.

Benefits

• Medical, pharmacy, dental, and vision care.
• BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
• Flexible time off (unlimited, with manager approval, 11 paid national holidays)
• 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
• Unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree