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Diagnosis

• Valencia
• Hybrid
  
  

Prenatal Diagnosis

At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby.

Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment.

What You´ll Do

As part of our collaborative and high-performing prenatal diagnosis team, you will play a key role in the interpretation and management of genomic data across a range of diagnostic applications.

Your mission will be to analyse NIPT results using different bioinformatic algorithms, to process non-invasive products of conception (niPOC) samples through a dedicated analysis workflow, and to curate copy number variants (CNVs) from prenatal and postnatal chromosomal microarrays using the CHAS software (Thermo Fisher).

You will be responsible for generating and validating clinical reports, maintaining and updating the associated databases, and providing technical and interpretative support to Igenomix Group affiliates in the field of reproductive and prenatal genetics.

In certain cases, you will also contact doctors and patients to explain test results in detail, outlining their implications and suggesting appropriate next steps, ensuring clear, accurate, and empathetic communication of the findings.

Among Your Key Responsibilities

• Conduct analyses using Illumina and Thermo Fisher platforms (bioinformatic analysis and interpretation) for NIPT and CMA testing.
• Follow laboratory procedures for test analyses, ensuring accurate review and maintenance of patient test result records.
• Identify any issues that may adversely affect test performance or result reporting, and either correct the problems or immediately notify the general supervisor or laboratory director.
• Document all non-conformities and the corrective actions taken when test systems deviate from the laboratory’s established performance specifications.
• Communicate professionally with clients to provide or obtain the information required for testing, including guidance on test selection, ordering, and pre- and post-analytical steps.
• Observe analytical and post-analytical procedures (when required) and ensure that proper documentation (such as reports) is completed and maintained.
• Be available to work weekends, depending on workload and operational needs.
• Maintain an organized and responsible work approach to ensure all laboratory testing is performed safely and efficiently.
• Ensure proper record keeping and quality control procedures are followed.
• Participate in the validation of new tests or test updates.
  
  

What We’re Looking For

• Bachelor’s, Master’s, or Doctoral degree in Biomedical Sciences, Biology, or a related field from an accredited institution.
• Solid knowledge of laboratory techniques and the use of diagnostic equipment.
• Membership in a State Biologists Professional Body (or similar professional organization) to be eligible to sign reports, or willingness and eligibility to obtain such membership upon selection.
• Knowledge of pre- and post-test genetic result interpretation and communication will be valued.
• Excellent Spanish (oral and written) and a good command of English, both spoken and written.
• Ability to communicate professionally with clients, providing and retrieving the information required for testing.
• Skills in scientific writing, data analysis, statistics, and the use of bioinformatic tools or genomic data interpretation software will be positively valued (not essential).
• A proactive and resilient team player with strong problem-solving and people management skills, able to handle unexpected situations and manage interpersonal challenges effectively.
• Ability to work effectively in a multidisciplinary and international environment.
• Strong sense of initiative and adaptability in a dynamic and evolving laboratory setting.
  
  

Why Vitrolife Group?

Because here, your work truly matters. You’ll be joining a team where:

• meets purpose, and every project is guided by the desire to help more people fulfill their dream of having a baby.
• Learning never stops, and you’ll have opportunities to grow professionally while contributing to a meaningful mission.
• Global collaboration is part of our DNA, you’ll work with colleagues across countries in a multicultural, inclusive environment.
• Quality, integrity, innovation and collaboration are not just words, they’re the foundation of how we work and grow together.
  
  

What We Offer

• Opportunity to work in a leading global organization in healthcare and genetic services.
• Supportive and collaborative work environment.
• Training opportunities for candidates without direct experience in some areas.
• Medical insurance.
• Flexible compensation options.
• Free coffee at the workplace.
• Flexitime.
• Discounts on our platform and gym memberships.
• Job stability in a growing and innovative company.
• The interview will be conducted in English
• The employee will be based in Valencia (Parque tecnológico de Paterna).
  
  

We look forward to receiving your application!

We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.

Department Diagnosis Locations Valencia Remote status Hybrid Employment type Full-time

About Vitrolife Group

Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We are supporting our customers by improving their clinical practice and the outcome of the patient’s fertility treatment.

Currently, we are approximately 1,100 people worldwide, headquartered in Gothenburg, Sweden. Vitrolife Group’s products and services are available in more than 125 countries, through our own presence in more than 25 countries and a network of distributors. We are a sustainable market leader and aim to be the preferred partner to the IVF-clinics by providing superior products and services with the vision to enable people to fulfill the dream of having a healthy baby.

The Vitrolife AB (publ) share is listed on the Nasdaq Stockholm.

Diagnosis

• Valencia
• Hybrid
  
  

Prenatal Diagnosis

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