Global Operational Quality Specialist

Posted 2 Days Ago
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Greenwood, SC, USA
In-Office
Expert/Leader
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role
Coordinates global operational QA/QC governance, harmonizes quality standards and processes, oversees CAPA and quality-risk escalation, and drives inspection readiness across sites. Leads global quality plans, training frameworks, change management, quality culture initiatives, and continuous improvement. Requires extensive GMP-regulated experience, expertise in QMS, LIMS, validation, product release, data integrity, and regulatory expectations, plus strong stakeholder-management and analytical capabilities. Travel is required up to 10%.
Summary Generated by Built In

 

The Global Operational Quality Specialist coordinates and drives the consistent execution of Operational Quality Assurance/Quality Control (QA/QC) processes across the global network. The role ensures effective implementation of quality governance, standards, performance monitoring, training, and quality systems through cross-functional collaboration with global and site quality teams.

The function supports harmonization of QA/QC practices, coordinates global quality initiatives, monitors execution, and drives timely follow-up of quality actions, risks, and improvement opportunities. The position also facilitates knowledge sharing, strengthens inspection readiness, and promotes sustainable operational quality performance across sites.

What you will do

  • Define and maintain the global Quality governance model, including governance structures, KPI/KQI frameworks, reporting processes, and inspection-ready performance management.

  • Coordinate global escalation processes, oversee CAPA governance and effectiveness, and drive follow-up of cross-site quality risks, critical quality events, and operational QA/QC issues.

  • Define, monitor, and coordinate execution of the Global Quality Plan, Annual Product Reviews, Management Reviews, and strategic quality initiatives aligned with business priorities.

  • Develop and drive global Quality Culture and Quality Excellence programs, including communication, best practice sharing, and execution governance across all sites.

  • Develop, implement, and continuously improve global QA/QC standards, corporate SOPs, product release frameworks, control strategies, and quality oversight models.

  • Drive global harmonization of quality practices through structured gap assessments, implementation follow-up, and inspection-ready quality standards across sites.

  • Define, implement, and maintain the global GxP training framework, including governance, curricula, training effectiveness, and Learning Management System processes.

  • Support the global coordination of critical quality events by establishing investigation principles, promoting robust root cause analysis, and defining technical expectations for CAPA effectiveness.

  • Lead quality change management for global operational quality processes by initiating global changes, performing quality impact assessments, and ensuring cross-site implementation.

  • Support business growth by providing QA/QC expertise for strategic initiatives, driving process optimization and digitalization, and embedding continuous improvement into operational quality practices.

What we are looking for

  • MSc in Pharmacy, Biotechnology, (Bio-)Engineering, Life Sciences, or a related scientific or technical discipline.

  • Minimum of 10 years of experience in a GMP-regulated environment, including global quality systems, operational QA/QC, quality governance, and cross-site quality initiatives.

  • Strong technical expertise in GMP, QMS, LIMS, product testing and release, validation, data integrity, inspection readiness, CAPA, change management, and regulatory expectations.

  • Proven ability to develop, harmonize, and implement global quality standards, governance frameworks, and operational quality processes, driving continuous improvement and operational excellence.

  • Strong analytical and digital capabilities, including KPI/KQI development, trend analysis, SharePoint, and digital reporting dashboards and automation tools to support data-driven decision-making.

  • Excellent coordination, stakeholder management, and communication skills, with the ability to influence across global QA, QC, Operations, Validation, and senior leadership while delivering practical, scalable, and sustainable quality solutions

  • Willingness to travel (up to 10%)

Skills Required

  • MSc in Pharmacy, Biotechnology, Bioengineering, Life Sciences, or a related scientific or technical discipline
  • Minimum 10 years of experience in a GMP-regulated environment
  • Experience with global quality systems, operational QA/QC, quality governance, and cross-site quality initiatives
  • Technical expertise in GMP, QMS, LIMS, product testing and release, validation, data integrity, inspection readiness, CAPA, change management, and regulatory expectations
  • Experience developing, harmonizing, and implementing global quality standards, governance frameworks, and operational quality processes
  • Strong analytical and digital capabilities, including KPI/KQI development, trend analysis, SharePoint, digital reporting dashboards, and automation tools
  • Excellent coordination, stakeholder management, and communication skills across global QA, QC, Operations, Validation, and senior leadership
  • Willingness to travel up to 10%
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The Company
HQ: Basel
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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