PGT-A / PGT-SR Specialist (m/f/d) in Paterna, Spain
5/13/2026
Perform nucleic acid extraction and NGS experimental procedures while ensuring compliance with quality standards like CLIA and ISO 15189. Analyze and technically validate PGT-A and PGT-SR results to ensure diagnostic reliability and traceability.
Working Hours
40 hours/week
Company Size
501-1,000 employees
Language
English
Visa Sponsorship
No
Your Responsibilities
At Centogene, we are looking for a PGT-A / PGT-SR Specialist to join our genetics laboratory dedicated to advanced genetic diagnostics. We are seeking a professional with proven experience in genetic diagnostic procedures, particularly in PGT-A and PGT-SR, capable of combining experimental laboratory work with result analysis and interpretation.The selected candidate will actively participate in all phases of the analytical and diagnostic process, ensuring the quality, traceability, and reliability of results, while directly contributing to the laboratory’s operational activities.
Main Responsibilities
Laboratory Area:
- Extraction, quantification, and qualification of nucleic acids from various biological samples.
- Execution of NGS experimental procedures following validated SOPs.
- Operation of automated sample processing platforms.
- Proper management and storage of samples under controlled conditions.
- Compliance with quality standards (CLIA, CAP, ISO 15189, among others).
- Accurate recording and documentation of all performed activities.
- Identification, communication, and documentation of incidents, deviations, or non-conformities.
- Participation in internal quality control activities.
- Strict adherence to biosafety regulations and occupational risk prevention standards.
- Analysis, interpretation, and technical validation of PGT-A and PGT-SR results.
- Strict adherence to validated protocols and compliance with established KPIs.
- Review of metrics, chromosomal profiles, and results derived from NGS technologies and other molecular methodologies.
- Ensuring traceability, analytical robustness, and reliability in diagnostic processes.
Your profile
Technical Requirements:- Bachelor’s or Master’s degree in Biology, Biotechnology, Biochemistry, or related fields. A Master’s degree and/or PhD will be considered an asset.
- Previous experience in analytical and diagnostic laboratories, especially in PGT-A / PGT-SR. Experience in PGT-M will be considered an advantage.
- Knowledge and application of Good Laboratory Practices (GLP).
- Familiarity with quality systems, traceability, and technical documentation.
- Experience in genetic diagnostics, report preparation, and the use of associated laboratory information systems.
- Strong attention to detail and precision in task execution.
- Analytical thinking and problem-solving skills.
- Clear, professional, and effective communication, both internally and with clinical collaborators.
- Teamwork and multidisciplinary collaboration skills.
- Responsible, proactive, and quality-oriented attitude.
Why us?
At CENTOGENE, we believe that scientific excellence, innovation, and talent are fundamental pillars in shaping the future of diagnostics.- Joining our team means becoming part of a leading international company in molecular genetics and advanced diagnostics, working within a highly specialized, technologically advanced environment committed to the highest standards of quality and diagnostic accuracy.
- Being part of an international organization strongly committed to innovation and scientific excellence
- Gaining access to advanced sequencing, automation, and diagnostic technologies
- Developing your professional career within a dynamic, demanding, and continuously evolving environment
- Becoming part of a corporate culture built on quality, scientific rigor, and continuous improvement
About us
With employees from over 50 nations, CENTOGENE is a truly international company with offices is in Rostock, Berlin, Delhi, Boston, Valencia, Belgrade, and São Paulo.
We were born to help diagnostic patients with rare disease and today we evolved to help patients of all clinical specialties to make bold progress with guided solutions for physicians, their patients and pharma partners.
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