Scientist, OSD Clinical Manufacturing

Bristol-Myers Squibb • New Brunswick, NJ

225d • $96,940 - $117,500 • Hybrid

About The Position

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. 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. Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time while operationalizing the innovative technologies that will deliver the transformative medicines of tomorrow. As a member of our team, you will get the chance to play a pivotal role to positively impact patients' lives while developing professionally to achieve your own career goals.

Requirements

• B.E./B.S. in Engineering or in a related science field.
• Experience in pharmaceutical manufacturing and/or formulation (3 years) required.
• Experience with solid dosage dose manufacturing, cGMPs, and product or process development is preferred.
• The ability to work in a GMP environment and the capability to plan and execute projects is required.

Responsibilities

• Effectively oversee batch execution and supervise technicians to ensure product is made in accordance with pertinent specifications and cGMP requirements.
• Adherence to group master manufacturing schedule and escalation to management when timelines are at risk.
• Generation and review of GMP documentation as necessary, including batch records, SOPs, Work Instructions, planned deviations, operation alerts, and CAPAs.
• Coordinate activities with other departments to ensure timely release of products.
• Interface with Pharmaceutics R D to ensure proper technical transfer and scale-up of formulae and processes into Clinical Manufacturing and out to commercial manufacturing.
• Complete batch feedback reports and provide recommendation for process, procedure, and batch record improvements to management.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree