Bioinformatician Job at KGTiger

Senior Bioinformatician

Location

Salary:

Not provided

Genome International Corp

Expiration Date

Until further notice

Requirements

4+ years of bioinformatics programming experience in an industry or academic setting
Demonstrated experience as scientific programmer
Very strong in Perl, Python, JAVA, C, C++, BioPerl, and shell in Linux environment
Experience in MySQL database design and development
Experience in web-based MVC application framework
Proficiency in object-oriented design and development
Experience in statistical programming using R preferably in genomics or genetic
Knowledge in Molecular biology and Biostatistics (preferable)

Job Responsibility

Collaborate with biologists to understand and document analytical and data management requirements
Clinical genetic data analysis and reporting
Conduct research, lead development of bioinformatics software tools and curated databases
Develop coherent and integrated software and databases for biological problems
Develop data-analysis strategies, write algorithms, and deploy computational tools for the exploration of large datasets
Develop bioinformatics pipelines for analyzing NGS and metabolomics data
Write programs to generate genome-wide datasets for statistical genetics
Analyze, review and modify programs to increase operating efficiency or to adapt to new requirements
Work with various technologies to develop software solutions as part of research infrastructure
Assist, collaborate, and consult with internal/external researchers on analyses of NGS data

Pharmaceutical Bioinformatician

Are you a data enthusiast with a passion for solving complex biological problems...

Location

Canada , Toronto

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Master’s or PhD in Bioinformatics, Computational Biology, Genomics, or a related field
Proven experience in bioinformatics within a pharmaceutical, biotech, or research setting
Proficiency in programming languages such as Python, R, or Bash
Familiarity with public biological databases (e.g., NCBI, Ensembl) and tools (e.g., Bioconductor, Galaxy)
Strong understanding of molecular biology, statistics, and data visualization
Excellent communication skills and ability to work in interdisciplinary team

Job Responsibility

Develop and maintain bioinformatics pipelines for the analysis of omics datasets (genomics, transcriptomics, proteomics, etc.)
Process, analyze, and interpret high-throughput biological data
Collaborate closely with cross-functional teams including biologists, data scientists, and IT specialists
Integrate diverse datasets to support biomarker discovery, target identification, and drug development
Ensure quality control, reproducibility, and documentation of analyses
Present complex data and insights in a clear and actionable format to scientific and non-scientific stakeholders

What we offer

An international community bringing together more than 110 different nationalities
An environment where trust is central: 70% of our leaders started their careers at the entry level
A strong training system with our internal Academy and more than 250 modules available
A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)

Fulltime

Product Management Intern

BillionToOne is seeking a Product Management Intern to to support objectives in ...

Location

United States , Menlo Park

Salary:

4333.00 USD / Month

BillionToOne

Expiration Date

Until further notice

Requirements

Currently pursuing a Master’s degree, ideally in business administration, biological sciences, engineering, or other related field
Experience in biotechnology or healthcare industry preferred
Command of product principles, techniques, and best practices
Solid analytical skills to interpret internal data and leverage external data sources
Comfortable working with highly technical teams, including software engineers, bioinformaticians, and data scientists
Excellent communication (verbal and written) and interpersonal skills, with the ability to collaborate effectively across teams and communicate complex concepts to stakeholders
Ability to adapt to an ambiguous and evolving internal and external environment

Job Responsibility

Product strategy and planning: Collaborate cross-functionally to develop product strategy, define success criteria, and create roadmaps
Data analysis: Conduct data analysis to inform a product roadmap and provide strategic recommendations
Project management and execution: Deliver quality products through scope definition, agile project management, and effective stakeholder communication
Communication and documentation: Create detailed specifications for the project team and develop clear business and technical documentation to support project efforts. Foster relationships across multiple teams, manage expectations, and communicate upwards
Collaboration with internal stakeholders: Closely collaborate with internal teams (including Client Services, Sales, Genetic Counseling, Software Engineering, and Lab personnel) to understand user requirements and facilitate project communication

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Free daily on-site lunches provided from top eateries
Latest and greatest hardware (laptop, lab equipment, facilities)
A variety of perks on campus (state of the art gym, restaurant)
Free on-site EV charging (compatible with all EVs, including Tesla)

New

Senior Data Engineer

ADC is a European data and AI consultancy with offices in the Netherlands, Swede...

Location

Denmark , København

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

4+ years of experience in Life Sciences industry as a Data Engineer, ideally gained in consulting or project-based work
A solid foundation in AWS/Azure, Databricks, Python, data modelling, testing and monitoring in production environments
Hands-on experience developing data pipelines for omics data, imaging data, or other scientific datasets
A quantitative academic background: Bioinformatics or similar fields
The ability to communicate with anyone in the room, breaking down complex ideas for technical and non-technical audiences
A proactive and entrepreneurial mindset: you’re eager to solve problems, innovate, and drive change
A collaborative spirit: You believe the best solutions come from diverse perspectives and supporting each other to raise the bar
Ability to work at the intersection of science, engineering, and business
Fluency in English

Job Responsibility

Design, build, and maintain scalable data pipelines for Life Science use cases such as omics, imaging, experimental, and clinical data
Work with complex, high-volume, and heterogeneous datasets, ensuring data quality, traceability, and reproducibility
Develop data solutions on cloud platforms (AWS and/or Azure) that follow modern engineering and security best practices
Contribute to and implement solutions using Databricks and modern data engineering frameworks
Support projects end-to-end, from early discovery and design through to production deployment
Collaborate closely with bioinformaticians, data scientists, AI engineers, and client stakeholders to co-create solutions that work in practice
Share knowledge internally and contribute to ADC's thought leadership in Life Sciences data and AI

What we offer

Impact you can point to: You’ll see your work in action and our projects change how organisations make decisions
Real responsibility, real support: You’ll work alongside experienced experts from the start, learning by doing with mentorship and feedback built in
The freedom to try new things: Spot a better way to build something? A smarter process? We want people who challenge the status quo
Collective Week: Once a year, we go on a workation with the whole ADC team. We work on pro bono projects, explore new ideas, and make the kind of memories you’ll want to talk about
Ownership opportunities: We offer a competitive salary and bonus structure, plus the opportunity to invest in the company and become a co-owner once specific conditions are met. We mean it when we say collective
A vibrant culture: Friday breakfast, sports, social events, and much more: a culture you’ll notice from day one

Fulltime

Application Scientist, Clinical Genomics

Saphetor’s mission is to enable anyone to find, share and use the most comprehen...

Location

France

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

Master’s or PhD in Human Genetics, Laboratory Medicine, Molecular Biology/Pathology, Life Sciences, or related field
Hands-on experience in clinical genomics workflows, including NGS library preparation, sequencing, and secondary and/or tertiary analysis in a clinical setting
Solid grasp of variant classification frameworks and a deep understanding of NGS workflows
Ability to simplify complex clinical genomics and bioinformatics concepts for clinicians, laboratory technicians, researchers, and IT professionals
Native in French
Proficiency in English

Job Responsibility

Pre-sales Support: Act as the technical “closer” by delivering expert demonstrations that bridge clinical needs with VarSome Premium and Clinical
you will own the customer evaluation process, solve “pain points” around variant analysis, and advise on lab equipment/system integrations
Post-sales Support: Lead onboarding sessions for geneticists and bioinformaticians to ensure rapid “time to value”
you will act as the primary lead for on-premises and private cloud deployments, coordinating infrastructure specifications (storage, network) between clients and our DevOps team
Workflow Optimization & Support: Fine-tune filtering strategies and automation to maximize platform “stickiness” while acting as a high-level bridge between customer support and stakeholders to ensure seamless routine operations
Scientific Advocacy: Systematically gather power-user feedback to influence the product roadmap and cultivate strategic relationships for conference presentations (ESHG, MedTech) and the development of technical white papers
Cross-functional Collaboration: Partner with Product, Marketing, and Operations to ensure product-market fit and growth. Work with growth marketers to translate features into benefits for prospects, while influencing the product roadmap through prioritization

What we offer

A position in a fascinating healthcare growth domain, at the cutting edge of technology and research
A competitive compensation package tailored to your unique expertise and professional background
A remote-first work environment that promotes a healthy work-life balance
Endless learning opportunities, while transferring new technologies from academics to clinical practice all over the world

Fulltime

Application Scientist, Clinical Genomics (Italy)

We are looking for an Application Scientist in Clinical Genomics to join our com...

Location

Italy

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

Master’s or PhD in Human Genetics, Laboratory Medicine, Molecular Biology/Pathology, Life Sciences, or related field
Hands-on experience in clinical genomics workflows, including NGS library preparation, sequencing, and secondary and/or tertiary analysis in a clinical setting
Solid grasp of variant classification frameworks and a deep understanding of NGS workflows
Ability to simplify complex clinical genomics and bioinformatics concepts for clinicians, laboratory technicians, researchers, and IT professionals
Native in Italian
Proficiency in English
Clinical Experience: Previous background in a hospital or private laboratory setting interpreting NGS patient cases
Regulatory Knowledge: Familiarity with working in regulated environments, such as IVDR, CLIA/CAP, or similar standards
Global Mindset: Proven experience in multicultural environments and/or supporting international customers in a scale-up setting

Job Responsibility

Pre-sales Support: Act as the technical 'closer' by delivering expert demonstrations that bridge clinical needs with VarSome Premium and Clinical
own the customer evaluation process, solve 'pain points' around variant analysis, and advise on lab equipment/system integrations
Post-sales Support: Lead onboarding sessions for geneticists and bioinformaticians to ensure rapid 'time to value'
act as the primary lead for on-premises and private cloud deployments, coordinating infrastructure specifications (storage, network) between clients and our DevOps team
Workflow Optimization & Support: Fine-tune filtering strategies and automation to maximize platform 'stickiness' while acting as a high-level bridge between customer support and stakeholders to ensure seamless routine operations
Scientific Advocacy: Systematically gather power-user feedback to influence the product roadmap and cultivate strategic relationships for conference presentations (ESHG, MedTech) and the development of technical white papers
Cross-functional Collaboration: Partner with Product, Marketing, and Operations to ensure product-market fit and growth
Work with growth marketers to translate features into benefits for prospects, while influencing the product roadmap through prioritization

What we offer

A position in a fascinating healthcare growth domain, at the cutting edge of technology and research
A competitive compensation package tailored to your unique expertise and professional background
A remote-first work environment that promotes a healthy work-life balance
Endless learning opportunities, while transferring new technologies from academics to clinical practice all over the world

Fulltime

IVD & CDx Validation Lead

Are you an experienced IVD professional specializing in NGS-based IVD and CDx pr...

Location

Switzerland , Rolle

Salary:

Not provided

SOPHiA GENETICS

Expiration Date

Until further notice

Requirements

Hands-on experience developing and validating NGS-based IVDs in a clinical diagnostic or CDx context
A thorough understanding of IVD analytical and clinical validation methodology: how to design studies that are fit for purpose, what guidance frameworks apply and when, and how to make and defend scope decisions
Working knowledge of FDA IVD regulatory pathways (510(k), De Novo, PMA, CTA/IUO) and/or EU IVDR, sufficient to design a validation program that holds up under regulatory review
Good working knowledge of statistics as applied to IVD V&V: familiar with the standard approaches across the main study types, and able to establish pragmatic, defensible methods. Deeper statistical expertise is a plus
Experience working within design controls and contributing to a Design History File
Clear, precise technical writing. Protocols and reports that are complete and reviewable without the need for extensive edits

Job Responsibility

Own the design and execution of validation programs for NGS-based IVD and CDx products, covering analytical performance, clinical performance, usability, and stability
Design studies that are fit for purpose: the right methodology, acceptance criteria, and statistical approaches based on what needs to be demonstrated and the applicable regulatory context, drawing on relevant guidance (CLSI, professional standards, etc) and your own experience
Handle the statistical aspects of V&V studies across the full range of study types - you know the standard approaches, when to apply them, and how to establish defensible methods. You do not need to be a dedicated biostatistician, but you need a solid command of the standard approaches
Produce DHF-ready documentation, written clearly enough to be reviewed without extensive back-and-forth
Build reusable validation frameworks, templates, and SOPs that can be applied consistently across programs
Be accountable for the technical success of CDx/CTA development programs end-to-end, from assay and bioinformatics pipeline development through verification, validation, and submission-ready regulatory evidence
Connect the development, validation, and regulatory sub-teams, to ensure efficient project delivery and effective project risk mitigation
Define the regulatory evidence strategy in collaboration with the Regulatory Lead: what is required, what is sufficient, what is not needed
Design the processes and standards that allow a growing diagnostics portfolio to be delivered consistently and efficiently across programs
Work closely with NGS scientists, bioinformaticians, regulatory, quality, and product colleagues across a highly cross-functional environment

What we offer

Sickness and Accident coverage through Helsana
Meal Vouchers at 90CHF PM with our partner cafeteria
A fun and engaging work environment, with Rest & Entertainment space, full stocked free coffee machine and free fruit/snacks
Free parking in an easy to access location
A strong social committee whose purpose is to make SOPHiA GENETICs both enjoyable as well as rewarding
As our global HQ, you’ll have direct interaction and exposure to senior leadership and our executive team locally

Fulltime

Ivd Development & Validation Lead

Are you an experienced IVD professional specializing in NGS-based IVD and CDx pr...

Location

Switzerland , Rolle

Salary:

Not provided

SOPHiA GENETICS

Expiration Date

Until further notice

Requirements

Hands-on experience developing and validating NGS-based IVDs in a clinical diagnostic or CDx context
A thorough understanding of IVD analytical and clinical validation methodology: how to design studies that are fit for purpose, what guidance frameworks apply and when, and how to make and defend scope decisions
Working knowledge of FDA IVD regulatory pathways (510(k), De Novo, PMA, CTA/IUO) and/or EU IVDR, sufficient to design a validation program that holds up under regulatory review
Good working knowledge of statistics as applied to IVD V&V: familiar with the standard approaches across the main study types, and able to establish pragmatic, defensible methods. Deeper statistical expertise is a plus
Experience working within design controls and contributing to a Design History File
Clear, precise technical writing. Protocols and reports that are complete and reviewable without the need for extensive edits
Experience in oncology diagnostics
Experience on CDx programs developed in partnership with pharma, including CTA and IUO studies
A track record of delivering V&V programs on tight timelines without compromising on what matters
Experience building validation infrastructure in a scaling environment: SOPs, templates, frameworks

Job Responsibility

Own the design and execution of validation programs for NGS-based IVD and CDx products, covering analytical performance, clinical performance, usability, and stability
Design studies that are fit for purpose: the right methodology, acceptance criteria, and statistical approaches based on what needs to be demonstrated and the applicable regulatory context, drawing on relevant guidance (CLSI, professional standards, etc) and your own experience
Handle the statistical aspects of V&V studies across the full range of study types - you know the standard approaches, when to apply them, and how to establish defensible methods
Produce DHF-ready documentation, written clearly enough to be reviewed without extensive back-and-forth
Build reusable validation frameworks, templates, and SOPs that can be applied consistently across programs
Be accountable for the technical success of CDx/CTA development programs end-to-end, from assay and bioinformatics pipeline development through verification, validation, and submission-ready regulatory evidence
Connect the development, validation, and regulatory sub-teams, to ensure efficient project delivery and effective project risk mitigation
Define the regulatory evidence strategy in collaboration with the Regulatory Lead: what is required, what is sufficient, what is not needed
Design the processes and standards that allow a growing diagnostics portfolio to be delivered consistently and efficiently across programs
Work closely with NGS scientists, bioinformaticians, regulatory, quality, and product colleagues across a highly cross-functional environment

What we offer

Sickness and Accident coverage through Helsana
Meal Vouchers at 90CHF PM with our partner cafeteria
A fun and engaging work environment, with Rest & Entertainment space, full stocked free coffee machine and free fruit/snacks
Free parking in an easy to access location
A strong social committee whose purpose is to make SOPHiA GENETICs both enjoyable as well as rewarding
As our global HQ, you’ll have direct interaction and exposure to senior leadership and our executive team locally

Fulltime

Bioinformatician

KGTiger

Location:

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 02, 2026

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KGTiger

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Category:IT - Software Development

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