KVALITO AG
jobid=A.0.0503
Join Our Team of Enthusiasts!
At KVALITO Consulting Group, a woman-owned business founded in 2013, we are dedicated to transforming the life sciences and healthcare sectors through tailored, innovative solutions that prioritize quality and people. Guided by our vision to lead with talent and transform with purpose, we are committed to creating lasting, high-value relationships with our clients and empowering high-performing individuals to reach their full potential.
At KVALITO, we embrace diversity, equity, and inclusion in every aspect of our work, fostering a results-oriented, ambitious, and caring culture. Our purpose-driven team is agile and adaptable, ready to learn and respond to evolving business needs. Together, we champion a culture that balances excellence with empathy, utilizing technology and human-centric approaches to drive impactful results.
If you’re passionate about making a difference and eager to grow within a company that values inclusivity and high performance, KVALITO could be the place for you. Join us in creating transformative solutions that empower our clients and leave a legacy of excellence in consulting.
Learn more about us at: #removed#
Life Science Consultant, Technician Quality Control
Position: Technician Quality Control
Location: Leiden, Netherlands
Role Overview:
As a 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.
Key Responsibilities:
- 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.
Key Qualifications:
- BSc or MSc degree in life sciences, biotechnology, or related discipline.
- 1 – 3 years working experience in a GMP QC setting in Biotech and/or Pharmaceutical Industry.
- 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.
- Self-driven and can-do mindset, without compromising quality.
- Fluent in English.
We offer great benefits
- Flat hierarchies and responsibility from the beginning
- People-oriented culture
- Diversity and inclusion-focused environment
- Global client projects in a multinational environment
- Flexible working hours and home office
- Involvement in global conferences
- Individual professional development, training, and coaching
We look forward to your application.
Your KVALITO Team.
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