Scientist, MS&T Process Characterization Lab Full-time

Scientist, Ms&T Process Characterization Lab

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. 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.

Position Summary

The Process Characterization Lab Scientist is a highly impactful and hands-on position within our global Parenteral Manufacturing Science & Technology organization, located in New Brunswick, NJ. The incumbent conducts product and process characterization studies; collaborates with research and development in drug product process development of sterile parenteral/biologics drug product and works with manufacturing sites to characterize, troubleshoot or optimize processes for late-stage to commercial and lifecycle products. The role touches many aspects of parenteral manufacturing including sterile filtration, formulation development/characterization, lyophilization, product compatibility and more. This gives the scientist the opportunity to contribute true scientific outcomes; enabling data driven decisions and scientifically sound manufacturing processes. This position is accountable for the design and execution of process characterization experiments to ensure design and transfer of robust manufacturing processes for new products and key life cycle management products, development of new technology for optimization and continuous improvement in manufacturing operations and providing specialized expertise, as necessary, to complement site capabilities for critical investigations or process improvements.

Key Responsibilities

• Design and execution of robust experiments to support lifecycle management activities of commercial parenteral products including: process improvements, deviation investigation and technology transfer
• Responsible for characterizing, optimizing and troubleshooting product and manufacturing processes of parenteral dosage forms
• Partner with Drug Product Development, Parenteral Launch and Sterile Capabilities, Process Engineering, manufacturing sites and Analytical colleagues in design and execution of experiments
• Apply scientific and/or technical skills and functional knowledge to complete laboratory work and data analysis/interpretation
• Drive scientific innovation and new approaches in the lab, through research in literature, internal/external forums and/or trainings
• Maintain complete and accurate laboratory notebook and protocol/report documentation by following applicable SOP and Policy requirements
• Effectively represent the Process Characterization Lab in various internal and external teams to present experimental plans, review results and provide technical recommendations
• Lead laboratory maintenance through tracking instrument calibration, maintaining stock of supplies, general lab cleanliness and organization
• Lead lab safety initiatives, inspections and training
• Support mentorship of others within group/team; train others on procedures

Qualifications & Experience

Education/Experience/ Licenses/Certifications:

• Bachelor's degree with 5-7 years of relevant experience. Master and Ph.D. is preferred but not required. Time spent in advanced degree program may consider as equivalent experience.

Required:

• Thorough hands-on experience in the laboratory and a broad understanding of sterile product (particularly biologics) formulation development, analytical methods commercial manufacturing unit operations
• Proficient in critical thinking, clear & concise technical writing (specifically in scientific study plans and reports) and verbal communication
• Ability to design and execute scientifically sound, hypothesis driven experiments

Demonstrated ability to:

• Troubleshoot, interpret and discuss data with strong scientific arguments, draw appropriate conclusions and identify logical next steps
• Work independently under minimal supervision for most tasks
• Participate in troubleshooting of routine problems and initiatives related to continuous improvement and development of new approaches/technologies
• Lead activities with other team members to achieve results
• Communicate effectively with manager and cross-functional teams/stakeholders
• Make presentations in multidisciplinary meetings, logically present information to convey clear messages

Desired:

• Working competency of Statistical Process Control and related tools (JMP/MiniTab/SAS)
• Familiar knowledge of quality systems, Quality by Design, validation principles for product and engineering design and process control fundamentals

This position requires up to 10% of travel (occasional, as required).

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.

New Brunswick – NJ – US: $91,900 – $111,364

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit careers.bms.com/life-at-bms/.

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

• Health Coverage: Medical, pharmacy, dental, and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financial Well-being and Protection: 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.

Work-life benefits include:

• Paid Time Off
• US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
• Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include 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.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

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 a supportive culture, promoting global participation 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

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company