Senior Engineer I, MSEO Automation and Data Analytics
Bristol Myers Squibb
August 24, 2026
Remote friendly (Summit, NJ)
United States
IT
Shift Available:
- Monday–Friday 9:00am–5:00pm
Responsibilities:
- Act as a subject matter expert in data analytics with Manufacturing and Technical teams.
- Define, prioritize, and document business needs and solution requirements; partner with BI&T to develop data analytics/data science solutions.
- Create dashboards/visualizations; perform ad-hoc analysis to support operational and business decisions.
- Provide technical direction to Site teams to improve capacity, quality, and cost; support root-cause investigations.
- Establish and maintain service level expectations across site functions and systems.
- Support automation/data intake assessment and backlog management; align work to site objectives and network policies.
- Deliver network improvements (recipe updates, data analysis reports) and provide MES product impact assessments.
- Develop/configure digital solutions (e.g., electronic batch records, process automation) across the solution lifecycle.
- Support lifecycle management and site project implementation.
- Translate business requirements into compliant functional/design specifications.
- Lead change management and support process improvement and automated system modifications.
- Support manufacturing systems incidents, quality investigations, impact assessments, and process monitoring.
- Lead QMS deliverables (SOPs, work practices, training, Change Controls/Actions, CAPAs, technical reports).
- Support CPV, process monitoring, technical transfer, and automated system lifecycle activities.
- Interface cross-functionally; act as Manufacturing Automation System Business Owner as applicable and participate in plant meetings.
- Ensure compliance with global regulatory and cGMP requirements; support inspections.
- Coach/mentor team members and promote compliance.
Knowledge & Skills (selected):
- Leadership/coaching, strategic planning, strong communication, organizational/time management.
- MS Office; proficiency in Tableau/Power BI.
- cGMPs and biopharmaceutical regulations; cell therapy experience preferred.
- Knowledge of manufacturing processes and ERP/PCS/MES relationships.
- Working knowledge of EBR, RBE, MES recipe lifecycle; HP ALM/EDMS/Change Mgmt systems preferred.
- SQL and Python (or R) preferred; CAR-T/biopharma manufacturing and QC preferred.
- Ability to travel 10%–15%.
Minimum Requirements:
- Bachelor’s degree in Engineering, Biological/Life Sciences, Chemistry, Biochemistry, or related field (or equivalent).
- 6+ years in manufacturing support/engineering in biotech/pharma.
- 2+ years leadership/supervisory experience preferred.
Compensation: $106,810–$129,430 (Summit West – NJ – US).
Application Instructions: Apply via the role posting on BMS careers; include any required local information requested in the posting.
- Monday–Friday 9:00am–5:00pm
Responsibilities:
- Act as a subject matter expert in data analytics with Manufacturing and Technical teams.
- Define, prioritize, and document business needs and solution requirements; partner with BI&T to develop data analytics/data science solutions.
- Create dashboards/visualizations; perform ad-hoc analysis to support operational and business decisions.
- Provide technical direction to Site teams to improve capacity, quality, and cost; support root-cause investigations.
- Establish and maintain service level expectations across site functions and systems.
- Support automation/data intake assessment and backlog management; align work to site objectives and network policies.
- Deliver network improvements (recipe updates, data analysis reports) and provide MES product impact assessments.
- Develop/configure digital solutions (e.g., electronic batch records, process automation) across the solution lifecycle.
- Support lifecycle management and site project implementation.
- Translate business requirements into compliant functional/design specifications.
- Lead change management and support process improvement and automated system modifications.
- Support manufacturing systems incidents, quality investigations, impact assessments, and process monitoring.
- Lead QMS deliverables (SOPs, work practices, training, Change Controls/Actions, CAPAs, technical reports).
- Support CPV, process monitoring, technical transfer, and automated system lifecycle activities.
- Interface cross-functionally; act as Manufacturing Automation System Business Owner as applicable and participate in plant meetings.
- Ensure compliance with global regulatory and cGMP requirements; support inspections.
- Coach/mentor team members and promote compliance.
Knowledge & Skills (selected):
- Leadership/coaching, strategic planning, strong communication, organizational/time management.
- MS Office; proficiency in Tableau/Power BI.
- cGMPs and biopharmaceutical regulations; cell therapy experience preferred.
- Knowledge of manufacturing processes and ERP/PCS/MES relationships.
- Working knowledge of EBR, RBE, MES recipe lifecycle; HP ALM/EDMS/Change Mgmt systems preferred.
- SQL and Python (or R) preferred; CAR-T/biopharma manufacturing and QC preferred.
- Ability to travel 10%–15%.
Minimum Requirements:
- Bachelor’s degree in Engineering, Biological/Life Sciences, Chemistry, Biochemistry, or related field (or equivalent).
- 6+ years in manufacturing support/engineering in biotech/pharma.
- 2+ years leadership/supervisory experience preferred.
Compensation: $106,810–$129,430 (Summit West – NJ – US).
Application Instructions: Apply via the role posting on BMS careers; include any required local information requested in the posting.