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Lonza

Global life sciences contract manufacturer

Quality Control Technical Expert – Microbiology

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeGeleen, Netherlands€46.5k - €65.1k /yrIn-person

About the Job

Requirements

  • A bachelor's or master's degree in microbiology or a closely related scientific discipline.
  • Substantial experience in pharmaceutical microbiology within a GMP-regulated Quality Control environment.
  • Strong practical experience with pharmaceutical microbiology test methods across different sample types, including working with bacteria, yeasts and moulds, as well as environmental monitoring, bioburden and water testing.
  • Experience writing and reviewing GMP documentation, with a sound understanding of applicable microbiological guidelines and quality requirements.
  • Strong analytical and problem-solving skills to assess microbiological risks and resolve technical issues.
  • Clear communication and strong collaboration skills, with the confidence to advise colleagues, share expertise and explain technical topics during audits.
  • Strong organizational and planning skills, with the initiative to improve quality and efficiency.
  • Business-fluent English is required.

Responsibilities

  • Act as a technical expert for pharmaceutical microbiology, advising QC colleagues, Manufacturing and other stakeholders on complex issues and microbiological risk assessments.
  • Perform and support microbiological testing and environmental monitoring activities, including bioburden analysis, water sampling and testing.
  • Coordinate the planning and execution of microbiology activities with colleagues, providing technical guidance to ensure work is completed and reported on time.
  • Write, review and approve GMP documentation, including procedures, protocols and reports, in collaboration with other departments.
  • Represent QC as a microbiology expert during internal and external audits, inspections and client discussions.
  • Support the implementation and validation of microbiological methods and associated systems, ensuring compliance with applicable GMP requirements.
  • Stay up to date with developments in pharmaceutical microbiology and work with QC colleagues and contract laboratories to improve testing, processes, planning and training, sharing knowledge across the department.

Desired Qualifications

  • Experience with method and system validation is an advantage.

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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