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Lonza

Global life sciences contract manufacturer

Global Operational Quality Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeGreenwood, SC, USANo salary listed

About the Job

Requirements

  • A Master of Science degree in Pharmacy, Biotechnology, Bio-Engineering, Life Sciences, or a related scientific or technical discipline.
  • A minimum of 10 years of experience in a Good Manufacturing Practice-regulated environment, including global quality systems, operational Quality Assurance and Quality Control, quality governance, and cross-site quality initiatives.
  • Strong technical expertise in Good Manufacturing Practice, Quality Management Systems, Laboratory Information Management Systems, product testing and release, validation, data integrity, inspection readiness, Corrective and Preventive Action, change management, and regulatory expectations.
  • Proven ability to develop, harmonize, and implement global quality standards, governance frameworks, and operational quality processes while driving continuous improvement and operational excellence.
  • Strong analytical and digital capabilities, including Key Performance Indicator and Key Quality Indicator development, trend analysis, SharePoint, and digital reporting dashboards and automation tools.
  • Excellent coordination, stakeholder management, and communication skills, with the ability to influence across global Quality Assurance, Quality Control, Operations, Validation, and senior leadership.
  • Willingness to travel up to 10%.

Responsibilities

  • Define and maintain the global Quality governance model, including governance structures, Key Performance Indicator and Key Quality Indicator frameworks, reporting processes, and inspection-ready performance management.
  • Coordinate global escalation processes, oversee Corrective and Preventive Action governance and effectiveness, and drive follow-up of cross-site quality risks, critical quality events, and operational Quality Assurance and Quality Control 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 Quality Assurance and Quality Control standards, corporate Standard Operating Procedures, 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 Good Practice 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 Corrective and Preventive Action 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 Quality Assurance and Quality Control expertise for strategic initiatives, driving process optimization and digitalization, and embedding continuous improvement into operational quality practices.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1897

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