Senior Packaging Manager

Bristol Myers SquibbNew Brunswick, NJ
$123,580 - $149,752Onsite

About The Position

Position plays a key role in pharmaceutical packaging as a member of cross-functional development programs supporting projects from concept through commercialization. Bristol Myers Squibb's purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Requirements

  • Bachelors (or Masters) degree in science, engineering, packaging or a related field with a minimum of 6 years relevant experience.
  • Proven record in pharmaceutical packaging technology, technology transfer, process development and packaging support/activities.
  • Ability to interact at all levels of the organization with proven influencing ability e.g. Regulatory, CMO etc to achieve goals.
  • Strong negotiation capability and ability to manage complex stakeholder networks.
  • Ability to understand business implications of technical decisions.
  • Must have in-depth knowledge of primary packaging processes, and process equipment for OSD blister packaging (PVC/Alu, Alu/Alu, Aclar/Alu) and HDPE/LDPE bottles and associated sealing; sterile and nonsterile liquids and semisolids (bottle filling, vial filling, tubes).
  • Knowledge of Characterization/Analytical Techniques for measuring critical quality attributes of packaging materials.
  • Experience of methods for optimum primary and secondary packaging assessment.
  • In-depth knowledge of the regulatory standards and compliance expectations for such processes.
  • Knowledge of serialization requirements and serialization technology.
  • Experienced with use of statistical software to analyze process related data to determine process capability or for troubleshooting purposes.
  • Proficient in the technical transfer of packaging processes to CMOs within budget and according to project timeline. Demonstrated ability to manage one or more tech transfer projects with minimal supervision.
  • Excellent verbal, written communications and presentations skills, including excellence at concise writing of complex study plans and scientific reports; informing stakeholder groups about the critical issues related to packaging processes when required.
  • Ability to work on own and as part of a team and to drive issues to resolution.

Responsibilities

  • Provide Packaging technical support to the External Manufacturing Organization (ExM) and CMOs
  • Ensure the transfer of robust Primary and Secondary Drug Product Packaging processes to Contract Manufacturing Organizations (CMO)
  • Assess and maintain robust packaging process performance at CMO for the primary and secondary packaging of BMS products
  • Actively works to continuously reduce supply risks associated with packaging operations and processes
  • Maintains current knowledge of primary and secondary packaging types/technology, packaging processes, packaging equipment and serialization, to support successful operation of the ExM business unit
  • Support CMO selection process – compilation of technical packages, due diligence and completing scoring.
  • Leads packaging robustness assessment and improvement initiatives
  • Accountable for/Leading technology transfer packaging projects, ensuring robust technical transfer within budget constraints, and completing associated regulatory filings.
  • Support operational management of packaging CMOs as per Supplier Relationship Management governance model
  • Provide on-going technical support to ExM / CMO to ensure compliance and security of supply – metrics review, deviation closure, CAPA effectiveness, change control review, APQR review, process improvement. Identify and Implement OPEX initiatives as necessary.
  • Leads process investigations when required, using structured root cause analysis tools.
  • Represents Manufacturing Technology on project teams and works closely with Supply Relationship Manager and project team members. Product robustness - technical lead for creation of process robustness monitoring plan, process control strategy, and provides technical oversight of TPM sites to ensure continuous process monitoring for all products in scope.
  • Supervise work of MS&T specialist(s), when required.

Benefits

  • wellbeing support
  • retirement and financial protection benefits
  • insurance offerings (medical, dental, vision, life and disability)
  • Flexible Time Off (FTO)
  • 11 paid company holidays
  • 160 hours of paid vacation annually
  • 3 optional holidays
  • paid sick leave
  • up to two paid volunteer days per year
  • summer hours flexibility
  • leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs
  • annual Global Shutdown between Christmas Day and New Year's Day
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