Job Overview: We are looking for a Molecular Biologist with hands-on experience in Next Generation Sequencing (NGS), particularly on Illumina platforms, to join our laboratory team. The role involves performing routine molecular workflows, preparing and maintaining SOPs, and ensuring compliance with quality standards. Key Responsibilities: Carry out DNA/RNA extraction, library preparation, sequencing runs, and quality checks using Illumina platforms. Prepare, document, and maintain Standard Operating Procedures (SOPs) for NGS and related molecular assays. Ensure all laboratory processes follow quality assurance and quality control (QA/QC) requirements in line with international standards. Maintain accurate laboratory records, documentation, and reports. Support validation and optimization of molecular assays as required. Stay up to date with best practices in NGS and molecular laboratory workflows. Qualifications & Requirements: Master's degree in Molecular Biology, Genetics, or a related field. minimum of 2-3 years of experience with NGS workflows, preferably on Illumina sequencing platforms. Strong understanding of SOP preparation and laboratory quality systems. Proficiency in core molecular biology techniques (PCR, qPCR, library prep, nucleic acid extraction). Detail-oriented with good organizational and communication skills. Ability to work effectively in a laboratory team environment. Employment Terms: Full-time, on-site position in Saudi Arabia. Relocation package fully covered by the company, including visa processing, travel, and accommodation assistance. Benefits: Competitive salary and benefits package. Comprehensive health insurance. Professional development opportunities. Collaborative and supportive work environment.
Job Summary: We are looking for a skilled and motivated Bioinformatician to join our team on a full-time remote basis. The ideal candidate will play a key role in analyzing large-scale biological and genomic datasets, developing and maintaining bioinformatics pipelines, and supporting both research and clinical projects. This position requires a strong background in computational biology, data analysis, and an excellent understanding of molecular and genomic data. Key Responsibilities: Analyze and interpret NGS (Next-Generation Sequencing) data, including DNA, RNA, and whole-exome or whole-genome datasets. Develop, optimize, and maintain automated bioinformatics workflows and pipelines. Perform variant annotation, filtering, and interpretation according to clinical or research standards. Collaborate with scientists, clinicians, and software engineers to design and implement data analysis solutions. Ensure accuracy, reproducibility, and quality control in all analyses. Prepare detailed reports, data visualizations, and documentation for internal and external use. Qualifications: Bachelor’s or Master’s in Bioinformatics, Computational Biology, Molecular Biology, or a related field. 2-3 years of experience in NGS data analysis (WES/WGS, RNA-Seq, or targeted panels). Proficiency in bioinformatics tools (e.g., GATK, BWA, SAMtools, VEP, STAR). Strong programming and scripting skills (Python, R, Bash). Familiarity with genomic databases (ClinVar, gnomAD, Ensembl, COSMIC, dbSNP). Excellent analytical and problem-solving skills. Ability to work independently in a remote, fast-paced environment. Experience with cloud platforms (AWS, GCP, or Azure). Knowledge of ACMG/AMP variant classification guidelines. Familiarity with containerization tools (Docker, Nextflow, or Snakemake).
Job Summary: We are looking for a skilled and motivated Bioinformatician to join our team on a full-time remote basis. The ideal candidate will play a key role in analyzing large-scale biological and genomic datasets, developing and maintaining bioinformatics pipelines, and supporting both research and clinical projects. This position requires a strong background in computational biology, data analysis, and an excellent understanding of molecular and genomic data. Key Responsibilities: Analyze and interpret NGS (Next-Generation Sequencing) data, including DNA, RNA, and whole-exome or whole-genome datasets. Develop, optimize, and maintain automated bioinformatics workflows and pipelines. Perform variant annotation, filtering, and interpretation according to clinical or research standards. Collaborate with scientists, clinicians, and software engineers to design and implement data analysis solutions. Ensure accuracy, reproducibility, and quality control in all analyses. Prepare detailed reports, data visualizations, and documentation for internal and external use. Qualifications: Bachelor's or Master's in Bioinformatics, Computational Biology, Molecular Biology, or a related field. 2-3 years of experience in NGS data analysis (WES/WGS, RNA-Seq, or targeted panels). Proficiency in bioinformatics tools (e.g., GATK, BWA, SAMtools, VEP, STAR). Strong programming and scripting skills (Python, R, Bash). Familiarity with genomic databases (ClinVar, gnomAD, Ensembl, COSMIC, dbSNP). Excellent analytical and problem-solving skills. Ability to work independently in a remote, fast-paced environment. Experience with cloud platforms (AWS, GCP, or Azure). Knowledge of ACMG/AMP variant classification guidelines. Familiarity with containerization tools (Docker, Nextflow, or Snakemake).
Job Overview: We are seeking a highly motivated Genome Analyst to join our team and support the analysis, interpretation, and reporting of genomic data. The ideal candidate will have strong technical expertise in molecular genetics and bioinformatics, with the ability to translate complex genomic findings into clear, clinically meaningful insights. Key Responsibilities: Perform high-quality analysis of whole exome, whole genome, and targeted gene panel sequencing data. Review and interpret variants according to ACMG/AMP guidelines and company standards. Generate clear, accurate, and clinically relevant genetic reports for physicians, clients, and internal teams. Collaborate with laboratory scientists, bioinformaticians, and clinical teams to ensure timely and accurate case review. Maintain up-to-date knowledge of genetic databases, variant classification tools, and the latest literature. Participate in weekly case discussions, multidisciplinary meetings, and continuous quality improvement activities. Ensure all analyses and reports comply with internal SOPs, quality standards, and data privacy regulations. Qualifications: Bachelor’s or Master’s degree in Genetics, Genetic Counseling, or a related field. Strong understanding of human genetics, variant interpretation, and genomic technologies. Hands-on experience with NGS data interpretation is highly preferred. Familiarity with ClinVar, gnomAD, HGMD, OMIM, Varsome, or similar genomic databases and tools. Excellent analytical thinking, attention to detail, and problem-solving skills. Strong written and verbal communication skills in English. Ability to work independently, manage time effectively, and meet deadlines in a fully remote environment.