Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But 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 rich in diversity. 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. Read more: careers.bms.com/working-with-us.

PMS&T Senior Scientist provides technical support for tech transfer, process validation, and commercial oversight for the manufacture of oral solid dosage forms at both internal BMS sites and at Contract Manufacturing Organizations (CMOs). The individual coordinates project activities and manages and coordinates change requests and process deviations.

This position reports to the leader of the PMS&T Drug Product Development to Launch group. This position is located in New Brunswick, NJ.

Responsibilities

• Support CMO/vendor selection process – preparation of technical information packages, participation in due diligence and site assessments, technical evaluation of Requests for Information (RFIs) and Request for Proposal (RFPs).
• Accountable for technology transfer to contract manufacturing organizations.
• Support regulatory activities associated with changes to assigned products .
• Support operational management of CMO as per Virtual Plant Team (VPT) governance structure
• Provide ongoing technical support to ExM / CMO to ensure compliance and security of supply – metrics review, investigation close-out, change control review, Annual Product Quality Review (APQR) review, process improvement. Implement / OPEX initiatives as necessary.

Required Competencies

• Drug Product - expert in Oral Solid Dosage (OSD) product manufacturing.
• Excellent verbal, written communications and presentations skills, including excellence at writing complex study plans and scientific reports;
• In depth understanding of regulations concerning cGMP, manufacturing, validation, quality systems, equipment innovations, upgrades, and instrumentation.

Required Qualification(s) and Desired Experience

• A degree in science or a related field with a minimum of 4 years relevant experience.
• Skilled in pharmaceutical technology, technology transfer, process development and manufacturing support/activities.
• Experience of statistical software.
• Ability to interact at all levels of the organization with proven influencing ability e.g. Regulatory, Supply Chain, CMO, etc. to achieve goals.
• Ability to understand business implications of technical decisions.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.