Senior QA Scientist – Particle Analytical (Kymos Group)
Would you like to play a key role in a highly specialized GMP laboratory – the only one of its kind in Denmark?
At Particle Analytical, now part of the Kymos Group, you will join a growing organization where quality, science, and collaboration go hand in hand. You will work at the intersection of QA, laboratory operations, and international pharmaceutical clients – with real impact on both processes and people.
About us
Particle Analytical is a specialized contract laboratory with more than 25 years of expertise in solid-state and particle characterization.
We support pharmaceutical companies worldwide with method development, validation, routine GMP analysis, and scientific problem-solving – helping our clients understand how particle properties impact formulation and manufacturing.
Our techniques include laser diffraction, Raman microscopy (incl. MDRS), XRD, DSC, TGA, and advanced microscopy – and a wide range of additional specialized techniques.
As part of the Kymos Group, you will have access to a broader scientific network and international QA collaboration, while working from our site in Hørsholm.
The role
As our new Senior QA Scientist, you will be a key part of our QA function, working hands-on with quality processes while helping shape and strengthen our systems in a growing organization.
You will collaborate closely with technicians, QC scientists, and commercial colleagues locally, as well as QA and technical teams across Kymos.
This is a role for someone who enjoys combining structure and quality with a dynamic laboratory environment.
Your responsibilities
You will:
- Own and maintain the Quality Management System (QMS) and related documentation
- Review and approve analytical and technical documentation
- Handle deviations, OOS/OOT investigations, CAPAs, and change controls
- Support audits, inspections, and supplier qualification activities
- Ensure GMP compliance and promote data integrity (ALCOA+)
- Contribute to quality improvements, KPI tracking, and continuous development
- Support training and ensure adherence to SOPs
- Participate in quality agreements and external QA activities
In addition, you will be involved in the implementation and maintenance of LIMS as part of our ongoing system development.
Who you are
You bring solid QA experience from the pharmaceutical industry and are comfortable working in a GMP-regulated environment. You enjoy taking ownership, working across functions, and contributing to both operational quality work and system improvements.
You likely:
- Have at least 5 years of experience from the pharmaceutical industry within QA/GMP
- Have experience acting as QA responsible during audits and inspections
- Are fluent in English (written and spoken)
- Have a strong understanding of GMP requirements
It is an advantage if you:
- Have experience from QC or laboratory environments
- Speak Danish
- You can adapt and improve quality systems to meet corporate, customer, and regulatory requirements
- You think proactively and are able to foresee risks related to changes, methods, and processes
- You balance a strong overview of QMS with attention to detail in complex cases (e.g. deviations, OOS)
- You communicate openly and effectively across QA, QC, laboratory teams, and external stakeholders
Apply
If this role matches your experience and ambitions, we would be very interested in hearing from you.
Please submit your application and CV as soon as possible, as we review candidates on an ongoing basis.
If you have any questions about the position, you are welcome to contact Fozia Jabeen Shah for an informal discussion at +45 45 76 30 60.
We are looking forward to welcoming the right candidate to our team in Hørsholm.
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