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Lonza

Global life sciences contract manufacturer

Quality Control Program Coordinator

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timePortsmouth, NH, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in a scientific discipline is required.
  • Experience working in a pharmaceutical, biotechnology, or other regulated environment is required.
  • Project management experience coordinating multiple priorities and stakeholders is required.
  • Strong communication skills and the ability to build relationships across teams and with customers are required.
  • The ability to organize, prioritize, and drive projects to completion in a fast-paced environment is required.
  • Problem-solving skills and the ability to make informed decisions using available data are required.
  • A collaborative mindset and commitment to quality, customer service, and continuous improvement are required.

Responsibilities

  • Serve as the primary Quality Control representative for assigned customer programs and quality-related initiatives.
  • Lead project meetings, track deliverables, and drive action items to successful completion.
  • Partner with customers and internal stakeholders to ensure quality commitments are met.
  • Coordinate quality activities involving investigations, deviations, corrective and preventive actions, and change controls.
  • Communicate project status, risks, and timelines to customers and leadership teams.
  • Collaborate with Manufacturing, Quality Assurance, Manufacturing Science and Technology, and Program Management to support project objectives.
  • Support continuous improvement efforts that enhance quality, compliance, and customer satisfaction.

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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