Novartis

Novartis

Sr. Manager, Manufacturing Execution Systems (MES)

Durham · Senior

No sponsorshipDetected 77 days ago
Data AnalysisGMPFDA RegulatoryResearchCommunicationCollaborationMentoring

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Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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Files H-1B transfers

1 transfer filing in the last year, covering 1 worker. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

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About the role

  • This position will be located in Durham, NC and will be an onsite role.
  • Unlock the future of pharmaceutical manufacturing as a leader at the forefront of digital operations and manufacturing excellence.
  • As Senior Manager, Manufacturing Execution Systems (MES), you will play a critical role in enabling safe, compliant, and efficient production that helps bring innovative therapies to patients around the world.

Responsibilities

  • Lead strategy, governance, and operational oversight for MES across the site.
  • Oversee MES lifecycle management, including support, enhancements, upgrades, and system compliance.
  • Partner across Manufacturing, Quality, Engineering, and IT to resolve complex system challenges.
  • Drive continuous improvement using performance metrics, operational trends, and KPIs.
  • Support 24/7 manufacturing operations through effective MES troubleshooting and issue resolution.
  • Lead cross-functional projects, balancing resources and priorities to deliver business-critical initiatives.
  • Maintain audit-ready systems, documentation, procedures, and compliance practices.
  • Develop high-performing teams through coaching, talent development, and a culture of accountability.
  • We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Requirements

  • Bachelor's degree in Biological Sciences, Engineering, Information Systems, Automation, or a related technical field.
  • Minimum eight years of experience in manufacturing systems, MES, automation, or regulated manufacturing environments.
  • Experience within the pharmaceutical or biopharmaceutical industry.
  • Strong knowledge of GMP, FDA regulations, electronic manufacturing systems, and data integrity principles.
  • Excellent verbal and written communication skills with the ability to influence diverse stakeholders.
  • Experience with MES roadmaps, manufacturing data analytics, KPIs, and digital manufacturing transformation initiatives.
  • Experience supporting validation, change control, CAPAs, audit readiness, and regulatory inspections for GMP computerized systems.

Compensation

  • The salary for this position is expected to range between $108,500 and 201,500 annually
  • The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically.
  • Novartis may change the published salary range based on company and market factors.
  • Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.
  • $108,500.00 - $201,500.00

Benefits

  • US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.
  • In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

Equal opportunity

  • The Novartis Group of Companies are Equal Opportunity Employers.
  • The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities.
  • EEO Statement:
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This listing is sourced directly from Novartis's careers page and normalized into a canonical job model.