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Senior Manager, CDMO Operations

Viatris

San Antonio, TXOnsitePosted 15 days ago
Full TimeSenior LevelOperations & Supply ChainPharmaceutical
Original posting ↗

Summary

Every day, we rise to the challenge to make a difference and here's how the Senior Manager, CDMO Operations role will make an impact:

Job description

Key responsibilities for this role include:

  • Represent the Site Head in selected internal and external forums, ensuring consistent communication of priorities, expectations, and decisions.
  • Facilitate leadership meetings and strategic reviews focused on decisions, actions, and outcomes; ensure decisions are translated into clear organizational actions and communicated effectively.
  • Help resolve cross-functional conflicts and competing priorities and support organizational initiatives that improve engagement, accountability, talent development, and overall site performance.
  • Establish and maintain a disciplined operating rhythm for strategic initiatives and site priorities; track deliverables, dependencies, risks, and decisions across functions to ensure commitments are met.
  • Represent site priorities with global stakeholders and secure the resources, decisions, and support needed to achieve site objectives.
  • Serve as a trusted advisor and thought partner to the Site Head, providing objective perspectives, business insight, and recommendations.
  • Take ownership of delegated workstreams and issues, driving them to resolution with appropriate urgency and independence; anticipate issues and develop options and recommendations before escalation is required.
  • Build strong relationships with global and regional leaders across Operations, Quality, Technical Operations, Supply Chain, Finance, HR, Commercial, IT, Procurement, and other relevant functions.
  • Act as an extension of the Site Head of Operations in selected internal and external forums, ensuring consistent communication of priorities, expectations, and decision.
  • Establish and maintain a disciplined operating rhythm for critical strategic initiatives and site priorities.
  • Act as a catalyst for continuous improvement and organizational effectiveness.
  • Perform other duties as assigned by Head of Site Operations.

The minimum qualifications for this role are:

  • Bachelor's degree in engineering, science, business, operations, or a related discipline is required; advanced degree preferred.
  • Minimum 10 years of progressive leadership experience within biopharmaceutical manufacturing, CDMO, pharmaceutical, biotechnology, or a closely related regulated environment.
  • Proven track record leading strategic initiatives, transformation programs, operational improvement, or complex cross-functional business priorities.
  • Strong understanding of the operational and business dynamics of a regulated biopharmaceutical environment.
  • Experience in a CDMO or contract manufacturing environment; partnership with a Site Head, General Manager, Business Unit Leader, or equivalent executive; and experience across multiple functions such as manufacturing, operations, quality, technical services, supply chain, finance, or commercial operations is preferred.
  • Experience leading organizational transformation or modernization initiatives; working with global executive teams and international stakeholders; and Lean/Six Sigma, project management, or change management training is preferred.
  • Knowledge and experience in lean manufacturing/operational excellence, standardization, is preferred.

Requirements

  • Bachelor's degree in engineering, science, business, operations, or a related discipline
  • Minimum 10 years of progressive leadership experience within biopharmaceutical manufacturing, CDMO, pharmaceutical, biotechnology, or a closely related regulated environment
  • Proven track record leading strategic initiatives, transformation programs, operational improvement, or complex cross-functional business priorities
  • Strong understanding of the operational and business dynamics of a regulated biopharmaceutical environment
  • Experience in a CDMO or contract manufacturing environment
  • Experience across multiple functions such as manufacturing, operations, quality, technical services, supply chain, finance, or commercial operations
  • Experience leading organizational transformation or modernization initiatives
  • Lean/Six Sigma, project management, or change management training
  • Knowledge and experience in lean manufacturing/operational excellence, standardization

Benefits

  • Competitive Salaries
  • Inclusive Environment

Company overview

Viatris Inc. is a global pharmaceutical company formed in November 2020 through the merger of Mylan and Pfizer's Upjohn division. Headquartered in Canonsburg, Pennsylvania, the company operates with a mission to empower people worldwide to live healthier at every stage of life. Viatris uniquely bridges the traditional divide between generics and branded medicines, combining the best of both approaches to address healthcare needs globally. With approximately 32,000 employees worldwide, the company maintains a diverse portfolio of over 1,400 approved therapeutic molecules across key areas including cardiovascular, infectious diseases, oncology, immunology, CNS and anesthesia, women's healthcare, diabetes and metabolism, gastroenterology, respiratory and allergy, and dermatology. Viatris operates approximately 40 manufacturing sites across five continents, producing oral solid doses, injectables, complex dosage forms, and active pharmaceutical ingredients. The company's global supply chain is designed to reach patients in more than 165 countries and territories, supplying approximately 1 billion patients annually. Viatris focuses on expanding access to high-quality medicines while developing more complex and novel products to address unmet medical needs.

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