Laboratory Support Technician - #56661

The Opportunity

Executes SOP-driven scientific protocols and workflows at customer facilities (e.g. media/buffer prep, solvent/reagent mixtures, filtrations, material weighing, physical testing), ensuring consistency, data integrity, and adherence to regulatory standards. Tasks may also include preparing routine laboratory solutions, performing environmental monitoring and testing activities, and/or end-to-end handling of customer-designed chemical samples. May ensure operational readiness through routine checks, setup, breakdown and support of critical laboratory equipment. Addresses challenges that are often undefined or frequently changing, applying past experiences and selecting solutions from available alternatives. Collects, documents, and organizes data and observations, ensuring clarity and accessibility for review and analysis by research teams. Communicates with internal teams and customer contacts, providing or obtaining information that often requires detailed explanation and context.

Laboratory Technician

Location: Nijmegen, Netherlands

Contract: Full-time | Initial 1-year contract with the possibility of conversion to a permanent position

About The Role

We are looking for a motivated and detail-oriented Laboratory Technician to support production operations at our client's site in Nijmegen. In this role, you will be responsible for performing essential laboratory and cleanroom support activities that enable production teams to focus on critical manufacturing processes.

The successful candidate will play a key role in maintaining controlled environments, preparing materials and solutions, and ensuring operational readiness within a GMP-regulated setting. This position is ideal for someone with a scientific background who enjoys working in a hands-on laboratory environment and contributing to high standards of quality and compliance.

Key Responsibilities

• Perform cleanroom cleaning and disinfection activities in accordance with established procedures.
• Prepare cleaning and disinfection solutions for controlled and GMP-regulated areas.
• Provide support for GMP compounding and production activities.
• Ensure laboratory and production support tasks are completed accurately and on schedule.
• Maintain high standards of housekeeping, compliance, and documentation within controlled environments.
• Support operational readiness and contribute to the smooth running of production activities.
• Provide cross-functional support to other departments as required.
• Follow all safety, quality, and GMP requirements while performing daily activities.
• Contribute to continuous improvement initiatives that enhance efficiency and service delivery.
  
  

Qualifications

• Degree in a scientific discipline or equivalent relevant experience.
• Previous experience working in a laboratory, production support, or GMP-regulated environment is preferred.
• Experience performing similar laboratory or production support activities is highly desirable.
  
  

Skills & Competencies

• Proactive and effective communicator.
• Strong organisational and planning skills.
• Ability to work accurately and efficiently in a regulated environment.
• Comfortable following procedures and maintaining compliance standards.
• Strong attention to detail and commitment to quality.
• Ability to manage workload effectively and prioritise tasks.
  
  

Personal Attributes

• Enthusiastic, positive, and eager to learn.
• Flexible and adaptable to changing priorities and operational needs.
• Reliable and self-motivated with a strong work ethic.
• Team-oriented with the ability to collaborate effectively across functions.
• Demonstrates a high level of accountability and ownership.
• Committed to delivering high-quality work and supporting team success.
  
  

Working Environment

This role is primarily based within laboratory and GMP-controlled production environments. The position requires adherence to strict quality, safety, and cleanroom procedures, including the use of appropriate personal protective equipment (PPE) and gowning requirements.

What We Offer

• Opportunity to work within a dynamic and highly regulated scientific environment.
• Hands-on experience supporting critical production operations.
• Collaborative and supportive team culture.
• Opportunities for training and professional development.
• A full-time position with an initial 1-year contract and the potential for permanent employment based on performance and business needs.
  
  

If you are passionate about science, enjoy working in a laboratory environment, and want to contribute to high-quality production operations, we would love to hear from you.

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.

The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.

We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!

EEO Statement

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at [email protected] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

Privacy Policy

We will use the personal information that you have submitted to us in order to consider your application for the relevant role.

Your privacy is important to us. Please click here for our Privacy Policy which explains the purposes for which we will use your personal information and the ways in which we will handle and retain your information. It also explains the rights you have in relation to your information, and how to contact us with any queries or requests.

3rd Party Non-Solicitation Policy

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.