Genetics Consultant

Company Description

Enigma Genomics is a global leader in next-generation sequencing solutions, specializing in advanced artificial intelligence tools to decode the human genome. Recognized as a pioneer in utilizing cutting-edge AI, the company provides personalized genetic insights that enhance health and well-being. Leveraging technologies developed by renowned institutions such as Google AI and the Broad Institute of MIT and Harvard, Enigma Genomics delivers reliable clinical diagnostic genomics. With a focus on innovation, the company is committed to improving lives through genetic medicine.

Job Description

We are seeking a highly qualified Genetics Consultant to join our laboratory team. The successful candidate will be responsible for the review, and final authorization of clinical genetic reports. This role involves evaluating genetic test results, assessing variant classifications according to established clinical guidelines, and ensuring the accuracy and clinical relevance of reports prior to release to healthcare providers.

The Genetics Consultant will collaborate closely with laboratory and clinical teams to support high-quality genetic diagnostic services and maintain compliance with international laboratory standards.

Key Responsibilities

• Review and interpret genetic and genomic testing results.
• Evaluate and classify genetic variants according to recognized clinical guidelines (e.g., ACMG).
• Provide final review and sign-off of clinical genetic reports prior to release.
• Ensure accuracy, clarity, and clinical relevance of reported findings.
• Maintain compliance with laboratory quality standards and reporting procedures.
• Collaborate with clinical and laboratory teams regarding test interpretation and reporting.

Requirements

• PhD in Genetics, Genomics, Molecular Biology, or a related field.
• 5–10 years of experience in clinical genetics or molecular diagnostics laboratories.
• Board certification in Clinical Genetics/Genomics (e.g., ABMGG, EBMG, FRCPath or equivalent).
• Strong expertise in genetic variant interpretation and clinical report review.
• Experience with genetic reporting standards and clinical guidelines (ACMG or equivalent).