About us

As a leading contract research, development, and manufacturing organization (CRDMO), Ardena partners with pharmaceutical companies of all sizes—from emerging biotech to global industry leaders—united by the mission to help biopharma innovators navigate drug development with precision, quality, and speed, bringing their molecules from discovery to the clinic and market. Our fully integrated services span drug substance and drug product development, manufacturing, nanomedicine, bioanalytical services, clinical logistics, state research, fill & finish, and CMC regulatory support.

With a rapidly growing international footprint, Ardena is home to over 750 professionals across six strategic locations - Belgium (Ghent), the Netherlands (Oss and Assen), Sweden (Södertälje), Spain (Pamplona), and the US (Somerset, New Jersey). Our open and transparent culture is built on collaboration, ownership, and innovation, guided by our We CARE values. We foster a communicative environment where mutual respect, accountability, and excellence empower our team.

We are looking for skilled and motivated professionals eager to grow their careers in an exciting and fast-paced environment. Whether you’re an experienced expert or just starting out, Ardena provides a dynamic workplace where you can contribute to meaningful drug development projects, expand your knowledge, and be part of a global team committed to making a difference. As an international organization, we help you navigate a career path that expands your possibilities beyond borders, opening doors to personal and professional growth without limits. Your potential to grow is limitless with us.

For the Ardena Bioanalysis business unit based in Assen, The Netherlands, we are looking for a:

Project Technician (Project Coordinator) LC-MS/MS

Our bioanalytical laboratory is a highly specialized, GLP-compliant facility offering a wide range of bioanalytical services to global pharmaceutical partners, from early drug discovery to Phase IV clinical studies. Our mission is to provide precise quantitative and qualitative analyses of drugs and biomarkers in biological matrices using cutting-edge techniques, including LC-MS/MS, ligand-binding assays (ELISA), qPCR, and flow cytometry.

Our growing team of bioanalytical scientists brings expertise across diverse fields, covering small molecules, peptides, cells, and proteins—such as antibodies, antibody-drug conjugates, oligonucleotides, and nanoparticles.

Your Role

As a Project Technician LC-MS/MS, you are responsible for coordinating bioanalytical studies. You work closely with the project manager and the laboratory technicians to ensure that projects are carried out efficiently and according to (GLP) quality standards. In addition to coordinating the practical aspects of a study, you are also responsible for material management, planning, documentation, and the release of studies.

Your Responsibilities

• Responsibility for the planning, preparation (including material management), execution, documentation, and quality control of assigned projects/studies.
• Keeping the project manager informed of the progress of the study.
• Instructing, training, and supporting technicians assigned to your studies.
• Coordinating daily activities with Team Managers Laboratory, Project Management, and Business Support (Planning).
• Ensuring the accuracy, integrity, quality, and confidentiality of study data.
• Responsibility for the evaluation and release of results.
• Ensuring compliance with SOPs, regulations, and the Study/Phase/Work Plan, and carefully document deviations.
• Collaborating with other departments and stakeholders to ensure efficient study execution.
• Assisting in writing and reviewing reports.
• Identifying and solving problems that arise during the execution of the study.
• Managing and efficiently allocating laboratory capacity to meet study requirements.
• Collaborating with other departments and fellow project technicians to implement continuous improvements and optimize study and lab processes.
• Contributing to a safe and healthy work environment by adhering to safety guidelines.
• Occasionally supporting practical laboratory work.

Your Profile

• Bachelor’s or Master’s degree (BSc or MSc) in a relevant field, or comparable practical experience that substantiates your knowledge and skills.
• Preferably at least 5 years of laboratory experience.
• Preferably available 32-40 hours per week.
• Demonstrable experience with regulated bioanalysis, including coordinating, documenting, and evaluating bioanalytical studies (but if you have less experience, we certainly encourage you to apply if you have a strong motivation to learn and grow).
• Experience in training and guiding new team members.
• Demonstrable proficiency in relevant laboratory techniques, equipment (LC-MS/MS), software (Analyst, Sciex OS), and data interpretation.
• Strong analytical and problem-solving skills.
• Preferably experience with and knowledge of a LIMS system.
• Thorough understanding of regulations (e.g., FDA, EMA, and ICH M10) related to bioanalytical studies.
• Strong knowledge of GxP guidelines (GLP and GCP).
• Experience with quality control steps and ensuring compliance with SOPs and regulations.
• Fluent in Dutch and English.

Your Skills

• Strong project management skills, including planning, organization, and time management.
• Strong ability to accurately and comprehensively document procedures, deviations, and results.
• Effective oral and written communication skills.
• Attention to detail to ensure the accuracy and integrity of study data and documentation.
• Flexibility to adapt to changing project requirements, timelines, and priorities.
• Strong collaboration and interpersonal skills.
• Ability to work autonomously.
• Values maintaining a safe and healthy work environment.
• Proactive, team player, problem-solving, decisive, sense of urgency.

What We Offer

• Salary range: € 3500,- to € 5000,- gross per month (based on a 40-hour workweek).
• A true learning environment where you will have the ability to grow your skills.
• A dynamic working environment with friendly and enthusiastic colleagues.
• A company culture with open communication, where employee well-being is highly valued.
• An attractive remuneration package
• Flexible working hours to support work-life balance.

Ready to apply? Please click on the application button.

Only candidates eligible to work in the EU will be considered for the position. Unfortunately, given the high volume of applications we receive for our vacancies, these professionals (not entitled to work in the European Union)  will not be given a status update. Agency calls will not be appreciated.