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Lonza

Global life sciences contract manufacturer

Aseptic Cleanroom Training & Excellence Specialist

Corporate & Technical TrainingConfirmed live in the last 24 hours
Full-timeGeleen, Netherlands€48.8k - €68.3k /yr

About the Job

Requirements

  • A Bachelor of Science degree or equivalent educational background in science or a related discipline.
  • Experience delivering Good Manufacturing Practice training.
  • Experience in a pharmaceutical, Good Manufacturing Practice, or similarly regulated manufacturing environment.
  • Knowledge of aseptic behaviour, sterile manufacturing practices, and relevant pharmaceutical regulatory requirements.
  • Experience with electronic GxP training platforms and the ability to develop and deliver effective training materials.
  • Strong communication and coordination skills to work effectively with employees, contractors, Manufacturing, and Quality Assurance stakeholders.
  • A self-starting, adaptable approach with strong attention to detail and the ability to manage changing priorities.
  • The ability to analyse trends, identify improvement opportunities, and translate findings into practical actions.
  • Willingness to work in a five-shift rotation model.

Responsibilities

  • Deliver and coordinate onboarding and Good Manufacturing Practice training focused on aseptic behaviour and maintaining an aseptic manufacturing environment.
  • Provide hands-on coaching to employees and contractors entering aseptic and classified manufacturing areas, including supporting the aseptic behaviour certification program.
  • Monitor aseptic practices, gowning techniques, and manufacturing activities to identify training needs and provide appropriate coaching or retraining.
  • Analyse trends and develop training materials and improvement actions to strengthen aseptic behaviour and training standards.
  • Support smoke studies, cleanroom management, and training and monitoring of personnel involved in cleaning activities.
  • Generate reports and trend analyses and support Manufacturing and Quality Assurance teams with aseptic training and compliance activities.
  • Support deviation investigations, corrective and preventive actions, risk assessments, and audits related to microbial contamination, aseptic procedures, and continuous improvement.
  • Evaluate equipment modifications, process changes, and new equipment or tools from an aseptic perspective, and support appropriate procedural revisions and assessments.

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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