
(Senior) Technician QC - Leiden (NL)
- On-site
- Leiden, Zuid-Holland, Netherlands
- Quality and Compliance
Job description
Pleased to meet you, we are Galapagos, a dynamic growing Biotech company with offices across Europe and in US, headquartered in Mechelen, Belgium.
We are in the business of changing lives. Focusing on high unmet medical needs, we synergize compelling science, technology, and collaborative approaches to create a deep pipeline of best-in-class medicines. With capabilities from lab to patient, including a decentralized cell therapy manufacturing platform, we are committed to challenging the status quo and delivering results for our patients, employees and shareholders. Our goal is not just to meet current medical needs but to anticipate and shape the future of healthcare, ensuring that our innovations reach those who need them most.
We pioneer for patients. We need thought leaders and rapid thinkers, entrepreneurs in spirit and status quo-fighters. Collaborative innovators and perseverant idealists. We need the best-in-class. In other words, we need you: The ‘make-it-happener’.
We are looking for a (Senior) Technician Quality Control to join our team. As our QC team is primarily based in Leiden, the Netherlands, you are ideally based near Leiden.
Scope of the job
As Technician, you are responsible for routine testing of our product and incoming goods using techniques for both analytical and microbiological testing such as Flow Cytometry, ELISA and PCR based methods. You also support method validation, method transfers, instrument maintenance and troubleshooting as well as taking an active role in implementing and following a GMP way of working.
Your role
Perform routine testing of samples for release, characterization, immune monitoring, incoming goods and environmental monitoring purposes
Perform method transfer, validation and qualification
Provide support for instrument maintenance and troubleshooting
Provide support in maintaining an efficient GMP laboratory
Take part in laboratory investigations
Support laboratory deviations
Participate in continuous improvement projects
Manage the availability of (critical) reagents and disposables for daily activities
Point of contact for questions related to lab practices and documentation
Write work instructions and SOPs
Job requirements
Who are you?
BSc or MSc degree in life sciences, biotechnology, or related discipline
Working experience in a GMP QC setting in Biotech and/or Pharmaceutical Industry is strongly preferred
Hands-on experience with flow cytometry, cell-based assays and PCR
Knowledge of microbiological methods is a plus
Strong interpersonal, verbal and written communication skills
Ability to be flexible with changing priorities and working schedules
Self-driven and can-do mindset, without compromising quality
Fluent in English
What’s in it for you?
At Galapagos, we prioritize your continuous growth and development, fostering a culture of empowerment. Our employees are the driving force behind our mission to lead in pharmaceutical research and innovation.
We offer a competitive compensation package and a supportive work environment with strong focus on your health and well-being. Join us in our journey towards sustainability, as we strive to make a lasting impact on both the industry and the planet.
Galapagos is dedicated to ensuring equal employment opportunities. Our hiring decisions are based on merit, considering qualifications, skills, performance, and achievements. We strictly prohibit discrimination against any employee or job applicant based on personal characteristics that are unrelated to their job.
We are Galapagos: together we can make it happen…!
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