Senior Principal Scientist – Packaging Engineering Full-time

Senior Principal Scientist – Packaging Engineering

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. 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 Senior Principal Scientist for Solid Oral Dose Packaging is a senior role within our pharmaceutical operations team. This position is responsible for overseeing and managing all aspects of solid oral dose packaging operations, ensuring the safe, efficient, and compliant production of pharmaceutical products by working closely with cross-functional teams to drive continuous improvement and innovation in the packaging processes for assigned projects.

Key Responsibilities

• Conducts tests with several packaging materials and final package for stability studies.
• Coordinate the packaging of stability supplies for new products.
• Provide technical expertise to the manufacturing teams, assisting with the resolution of problems associated with packaging/component equipment conflicts.
• Source, test, qualify and document new packaging components across a wide variety of types of materials and formats.
• Coordinates both internal and external resources to complete projects.
• Recommend improvements to packaging component design.
• Has in-depth knowledge of plastic injection molding and IBM and EBM molding manufacturing processes to provide guidance to suppliers to gain the correct desired outcome.
• Has in depth knowledge of thermoforming and cold form processes to provide guidance to suppliers.
• Works with packaging material suppliers to incorporate new areas of innovation into future development opportunities.
• Provide packaging technical assistance for quality and regulatory activities including developing test methods and preparation of technical documents for regulatory filings.
• Develop Instruction for Use and drive human factor studies for pediatric products.
• Responsible for driving the development of new technology to resolve packaging related issues.
• Responsible for successful project execution according to established objectives, timelines, and costs.
• This candidate must have the ability to manage multiple package development activities from concept through launch and be able to translate pharmaceutical and packaging industry trends to business opportunities.

Qualifications & Experience Required:

• Bachelor's degree in Packaging Science, Packaging Engineering, or Mechanical Engineering
• Minimum of 11 years of professional experience in the pharmaceutical or consumer products industry
• Primary Packaging Expertise: Demonstrated expertise in product primary packaging development, including plastic bottles and blister systems
• Technical Proficiency:
• Proven experience designing and developing primary packaging systems
• Hands-on experience authoring and executing packaging test protocols
• Familiarity with global packaging regulations and compliance requirements
• Track record of successfully managing complex, cross-functional packaging projects
• Strong verbal and written communication skills with the ability to thrive in multi-disciplinary team environments
• Self-directed, resourceful, and capable of managing multiple priorities with minimal supervision; proactively challenges existing practices to drive continuous improvement

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.

Compensation Overview:

New Brunswick – NJ – US: $140,200 – $169,888

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 https://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.
• *Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

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.