Process Engineer III Cell Therapy

Profile

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

PURPOSE AND SCOPE OF POSITION:

Key contributor to the development of Chimeric Antigen Receptor (CARs) phase-appropriate manufacturing process. This role will mentor junior members in the team and will support the planning, design and execution of development experiments to enable robust manufacturing process design. This role is responsible for phase-appropriate process development strategy formulation with support from manager/senior member of the team and drafting of appropriate regulatory filings.

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:

Education:

BS/ MS in Biological/Chemical Engineering, Biology or relevant scientific discipline

Experience


9 years for BS/ >7 years for MS of relevant experience


DUTIES AND RESPONSIBILITIES:


Lead the strategy and development of phase-appropriate manufacturing process with support from manager/ senior member of the teams. The goal is to develop robust manufacturing process that meets desired drug product quality.
Design and execute complex experiments using sound scientific principles and statistical approaches like Design of Experiments (DOE) to support efficient cell therapy process development and characterization effort.
Collaborate with analytical scientists and statisticians to analyze and interpret complex data in order to make sound scientific conclusion.
Troubleshoot and solve technical problems with minimal guidance from manager.
Support relevant process development laboratory activities.
Represent Process Development team in a cross-functional setting like technical team or CMC team to communicate process development activities progress, findings and to ensure all project deliverables are met.
Collaborate with Technology Transfer team for the transfer and implementation of new manufacturing process, new technology and other process changes to improve process robustness.
Maintain proficiency in data analysis and effective data presentation within a cross functional team setting.
Author and review appropriate sections of regulatory filings.
Author and review technical reports detailing experimental work and summarizing results
Maintain a safe work environment in accordance with policies/procedures/regulations
Mentorship or management of junior member(s) of the team.


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Company: Bristol-Myers Squibb

Req Number: R1526959_EN

Updated: 2020-07-08 00:00:00.000 UTC

Location: Seattle,Washington

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

Company info

Sign Up Now - WashingtondcCrossing.com