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Lonza

Global life sciences contract manufacturer

Quality Control Project Lead

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

About the Job

Requirements

  • A master’s degree or PhD in biology, biochemistry, pharmaceutical sciences, or a related natural science discipline.
  • Experience in a GMP-regulated environment and Quality Control is advantageous.
  • Strong planning and organizational skills, including the ability to manage competing priorities and remain focused under pressure.
  • Clear communication skills in German and English.
  • A collaborative, customer-oriented approach and the ability to work effectively across functions.
  • The ability to work independently, make sound decisions, and take ownership of project-related QC activities.
  • Confidence using MS Office; knowledge of systems such as Documentum, LIMS, or TrackWise is advantageous.
  • An adaptable and thorough approach to solving problems and delivering results.

Responsibilities

  • Represent QC in cross-functional project teams, independently coordinating QC activities and aligning priorities with QA, Operations, MSAT, and Engineering.
  • Establish and maintain strong customer relationships, acting as the primary contact for project-related QC matters.
  • Plan and oversee QC activities supporting production campaigns, ensuring readiness and timely delivery.
  • Coordinate, prioritize, and schedule tasks across analytical laboratories in line with project requirements and available resources.
  • Process change requests and deviations in accordance with GMP requirements.
  • Coordinate QC contributions to customer audits and regulatory inspections.
  • Calculate and monitor project-related QC costs, supporting cost-efficient delivery.
  • Collaborate closely with Program Management, Process Development, Manufacturing, and QA to resolve issues and adapt plans to changing priorities.

Desired Qualifications

  • Experience in a GMP-regulated environment and Quality Control is advantageous.
  • Knowledge of systems such as Documentum, LIMS, or TrackWise is advantageous.

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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