Senior MS&T Scientist - Parenteral Process Transfer Lead

Bristol Myers Squibb; Manatí (PR); Presencial; USD 107.000 - 129.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible Time Off (FTO)

11 paid holidays

160 hours vacation

Global Shutdown

Descripción de la vacante

Bristol Myers Squibb in Manati, Puerto Rico, is seeking a Principal Scientist, MS&T to own transfer, project management, optimization, and daily support of liquids and lyophilized parenteral manufacturing processes. You will ensure processes meet cGMPs and regulatory filings while coordinating with R&D, operations, and partners to hit timelines and quality targets.

As SME for end-to-end manufacturing, you will lead cross-functional teams, mentor junior scientists, and drive technology transfers

Formación

• Bachelor’s degree in Pharmacy, Engineering, Chemistry, or Science.
• 9–12 years of related Technical Services experience in pharma; Master’s 6–9 years; PhD 4–6 years.
• Three years experience in parenteral manufacturing of protein therapeutics.
• Excellent organizational and project management skills.
• Excellent communication in English and Spanish.

Responsabilidades

• Lead technology transfer activities for parenteral products.
• Manage cross-functional site teams to execute technical transfers.
• Develop and execute technology transfer plans aligning with schedules.
• Act as SME for liquid, lyophilized and syringe parenteral processes.
• Support site and R&D collaborations and regulatory submissions (CMC).
• Mentor junior scientists and drive site capabilities.

Conocimientos

Project management

Cross-functional leadership

Parenteral manufacturing

Biologics knowledge

English & Spanish

Educación

Bachelor’s degree in Pharmacy, Engineering, Chemistry, or Science

Descripción del empleo

Bristol Myers Squibb in Manati, Puerto Rico, is seeking a Principal Scientist, MS&T to own transfer, project management, optimization, and daily support of liquids and lyophilized parenteral manufacturing processes. You will ensure processes meet cGMPs and regulatory filings while coordinating with R&D, operations, and partners to hit timelines and quality targets.

As SME for end-to-end manufacturing, you will lead cross-functional teams, mentor junior scientists, and drive technology transfers