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Head of PGT-A/SR (m/f/d)

CENTOGENE GmbH

Valencia

Presencial

EUR 70.000 - 90.000

Jornada completa

Hoy
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Descripción de la vacante

A leading biomedical company in Spain is seeking an experienced professional to manage daily operations of the PGT-A/SR workflow. The role involves providing technical oversight, communication with clinics, and ensuring compliance with quality standards in a fast-paced laboratory environment. Candidates require a Bachelor’s or Master’s degree in a relevant field, alongside 3-5 years of experience in reproductive genetics laboratories. Proficiency in Spanish and English is also essential for effective collaboration.

Servicios

Competitive compensation package
Professional growth opportunities
Inclusive team culture

Formación

  • 3–5 years of experience in diagnostic or reproductive genetics laboratories.
  • Strong understanding of quality systems and documentation practices.
  • Native Spanish and English proficiency.

Responsabilidades

  • Manage daily operations of the PGT-A/SR workflow.
  • Act as a key point of contact for clinics and specialists.
  • Ensure strict adherence to SOPs and quality standards.

Conocimientos

Effective communication with clinicians
Organizational skills
Troubleshooting skills
Attention to detail

Educación

Bachelor’s or Master’s degree in Biology, Biotechnology, Genetics, Biomedical Sciences
Descripción del empleo
Your Responsibilities

Key Responsibilities

  • Manage daily operations of the PGT-A/SR workflow, ensuring adherence to TAT, quality standards, and processing capacity.
  • Execute the diagnostic activities within the PGT-A service, ensuring strict adherence to validated protocols and consistently meeting the established KPIs.
  • Coordinate staff schedules, workload distribution, and daily task assignments to ensure consistent operational readiness.

Clinical Communication & Service Excellence

  • Act as a key point of contact for clinics and fertility specialists, ensuring clear, timely, and professional communication.
  • Provide direct, accessible telephone support for any technical or documentation-related questions, promoting a high-quality and reliable service experience.
  • Coordinate with internal teams to ensure that clinical partners receive accurate information.

Quality, Compliance & Documentation

  • Ensure strict adherence to SOPs, quality standards, and regulatory requirements (ISO-based frameworks, internal QMS).
  • Support investigation and documentation of deviations, non-conformities, CAPAs, and change controls.
  • Maintain audit-ready documentation and assist during internal or external audits.

Technical Oversight (PGT-A/SR)

  • Provide technical supervision across the PGT-A/SR pipeline, ensuring correct execution of all processes and QC steps.
  • Troubleshoot technical issues, support root-cause analysis, and help implement corrective actions in coordination with QA and scientific teams.
  • Ensure consistent application of validated workflows, QC criteria, and result governance procedures.
  • Issue resolution, and seamless support throughout the PGT-A/SR process.
Your profile

Required Qualifications

  • Bachelor’s or Master’s degree in Biology, Biotechnology, Genetics, Biomedical Sciences, or related fields.
  • Minimum 3–5 years of experience in diagnostic or reproductive genetics laboratories (direct experience with PGT-A/SR workflows).
  • Strong ability to communicate effectively with clinicians and partner clinics, providing clear guidance in both technical and clinical contexts.
  • Previous experience in laboratory supervision or coordination.
  • Strong understanding of quality systems and documentation practices.
  • Native Spanish and English proficiency.

Key Competencies

  • Strong organizational skills and operational supervision.
  • Ability to guide, support, and develop technical staff.
  • Attention to detail and strong compliance mindset.
  • Effective troubleshooting and data-driven problem solving.
  • Clear and professional communication, both internally and with clinical partners.
Why us?
  • Opportunity to contribute to a mission-driven environment supporting reproductive genetics.
  • Professional growth in a high-impact laboratory setting.
  • Competitive compensation package aligned with experience.
  • Inclusive, collaborative, and international team culture.
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