We are a leading gastrointestinal health company delivering minimally invasive diagnostics to transform access to esophageal care. Our EndoSign test combines a simple, swallowable device with cutting-edge laboratory biomarkers and analytics to detect esophageal cancer and its precursor, Barrett’s esophagus.
Operating across the US and UK life-science hub, with hybrid, remote and onsite teams, we are expanding our pipeline to address new high-impact targets across gastroenterology and related fields. You’ll join a close-knit team of experts in our field who collaborate daily to translate breakthrough ideas into real-world solutions.
At Cyted Health, every voice matters. Whether you’re in R&D, Commercialisation, Medical Affairs or Operations, you’ll have the chance to lead projects, influence strategy, and broaden your skill set across the company. We champion diverse backgrounds and perspectives, fostering an inclusive culture where everyone can thrive and innovate.
If you’re inspired by purpose, motivated by challenge, and eager to make a meaningful impact on patient lives, we’d love to hear from you. We usually recruit on a rolling basis with the following four stages:
Initial Conversation – An online meeting with Maddie, a member of our People team, to learn about your skills & experiences and for you to explore what it is like to work with us.
Line Manager Interview – An online meeting with the hiring manager(s) to specifically discuss the role further.
Team Interview & Assessment – An onsite opportunity to meet the wider team, sometimes accompanied by an assessment or presentation on a topic related to the role.
Final Interview – An online meeting with our CEO to discuss your goals and the company’s history and vision.
As Cyted scales in the US, building a high-performing laboratory team to support the delivery of accurate and scalable diagnostic services is essential. This is an opportunity to join and contribute to this success from the start, where quality, efficiency, and patient outcomes are central to clinical impacts and sample processing.
We are therefore seeking a Molecular Technologist to operate within a hands-on wet lab environment. You will play a critical role in supporting end-to-end laboratory operations, including performing complex molecular assays, maintaining strict quality and compliance standards, and contributing to assay development and validation activities.
Whilst we grow, you will get the opportunity to provide training and mentorship to laboratory personnel across both US and UK sites. Collaborating cross-functionally with scientific, operational, and leadership teams, you will help drive operational excellence and deliver high-quality diagnostic results.
Working Pattern and Location
The role is a full-time position with a standard 40-hour working week, from the contract lab in Roswell, Atlanta.
The Molecular Technologist will also need to visit other company sites when and if required within the US and UK.
What you will be doing
Laboratory Operations & Testing
Perform routine and complex molecular diagnostic assays (including DNA/RNA extraction, quantification, PCR/qPCR, and NGS workflows)
Support pre-analytical sample handling and ensure accurate tracking, documentation, and data integrity throughout all laboratory processes
Conduct laboratory testing in compliance with CLIA, CAP, and applicable state regulations, adhering strictly to SOPs, quality standards, and HIPAA requirements
Operate, maintain, calibrate, and troubleshoot laboratory instrumentation to ensure optimal performance and minimal downtime
Facilitate communication with internal and external stakeholders for equipment maintenance and troubleshooting
Provide on-site operational support, and delegated participation in off-hours or emergent laboratory needs when required
Quality & Compliance
Create, review, and revise Standard Operating Procedures (SOPs), worksheets, and technical documentation to support laboratory operations
Participate in assay validation, verification, and implementation, including establishing QC metrics for laboratory-developed tests (LDTs)
Perform and support QA/QC activities, including routine quality checks, audits, and compliance initiatives to maintain CLIA/CAP standards
Contribute to laboratory safety programs and regulatory compliance initiatives
Identify and implement opportunities to optimize workflows, improve efficiency, and enhance laboratory quality systems
Training, Collaboration & Laboratory Development
Deliver hands-on training, mentorship, and competency assessments for laboratory personnel across US and UK sites, including laboratory safety and molecular techniques
Collaborate closely with laboratory leadership and cross-functional teams to support laboratory scale-up, technology transfer, and operational excellence
Work with laboratory supervisors and team members to optimize workflows and support operational efficiency
Participate in lab meetings, safety initiatives, and continuous improvement activities
Who you are?
We are seeking a proactive, hands-on, and detail-oriented Molecular Technologist who thrives in fast-paced laboratory environments and combines technical expertise with a strong commitment to quality and precision. The ideal candidate will have proven experience in molecular diagnostics or clinical laboratory settings, with the scientific knowledge, problem-solving ability, and collaborative mindset needed to support Cyted’s delivery of high-quality, scalable diagnostic services.
Therefore you will have:
A degree in Medical Laboratory Science, Molecular Biology, Biology, or a related life sciences field
ASCP certification (MB, MLS, or SMB) completed or in progress with confirmed exam date
Minimum 3+ years’ experience in a molecular, clinical, genetic, or similarly regulated laboratory environment, including work within accredited frameworks (e.g., CLIA, CAP, NYS or equivalent)
At least 2+ years of hands-on experience with Next Generation Sequencing (NGS) workflows in a clinical or production setting (including manual library preparation and Illumina platforms)
Experience working in audited environments with strong knowledge of quality systems, documentation, compliance requirements, and handling of PHI in line with HIPAA regulations
Experience translating manual molecular processes to semi-automated or automated platforms (advantageous)
Strong scientific and technical expertise in molecular biology techniques, with the ability to plan, troubleshoot, and make confident independent decisions in a laboratory setting
Solid understanding of clinical laboratory operations, including workflow efficiency, sample integrity, data accuracy and quality management systems for validation processes
Effective communication for collaborating across multi-disciplinary, remote teams (US and UK)
Proven ability to train and mentor laboratory staff through structured, hands-on training delivery
Proficiency in Microsoft Office applications, particularly Word and Excel, for documentation and data handling
How we work
At Cyted, how we work is just as important as the impact we create. Following our recent Series B fundraise and with increasing US expansion, we are entering a defining stage of growth. As a Molecular Technologist, you will play a critical role in supporting the delivery of accurate, high-quality diagnostic testing, helping to build and scale laboratory operations that underpin our clinical impact.
We care deeply about the clinicians, partners and patients our work ultimately serves. In this role, care means maintaining the highest standards of quality, precision and integrity in every aspect of laboratory work. You will ensure that samples are handled, processed and analysed with accuracy, whilst SOP and sample administration is given the same level of attention, contributing to reliable diagnostic results that clinicians and patients can trust.
We expect you to own your responsibilities with confidence and accountability. Working within a hands-on laboratory environment, you will take ownership of end-to-end testing processes, from sample preparation through to assay execution and data recording. You will confidently and independently troubleshoot, deciding the best approaches and solutions, ensuring quality and compliance are maintained as Cyted scales.
We aim high Cyted is growing quickly, and our laboratory operations must scale with us. You will support the optimisation of workflows, contribute to assay validation and implementation, and help identify opportunities to improve efficiency, reliability and turnaround times. By maintaining high technical standards and supporting continuous improvement, you will help strengthen the foundation of our diagnostic services.
You will be expected to dive deep into our molecular workflows and technologies. By developing a strong understanding of laboratory processes, instrumentation and quality systems, you will help ensure robust and reproducible results. You will collaborate closely with laboratory leadership and cross-functional teams to troubleshoot issues, support technology transfer and contribute to operational excellence.
We encourage everyone to challenge and commit As Cyted continues to build and scale its laboratory capabilities, your insights and ideas will help improve processes, strengthen quality systems and enhance laboratory performance. Working across teams and geographies, you will contribute to a culture of continuous improvement and scientific excellence.
Finally, we deliver This role requires precision, resilience and follow-through. From processing samples to supporting assay development you will stay dedicated to overcoming challenges as they arise - whether related to equipment, samples or workflows - and work proactively to resolve them, ensuring laboratory operations continue to run smoothly. Your work will directly impact the quality of Cyted’s diagnostic services and, ultimately, patient outcomes.
This is how we work at Cyted. If this sounds like an environment where you can contribute to cutting-edge diagnostics, build expertise in a growing laboratory function and help deliver meaningful clinical impact, we’d love to hear from you.
Benefits
At Cyted, we believe people do their best work when they’re supported, trusted, and cared for. We offer a comprehensive and competitive benefits package that reflects our commitment to your wellbeing, development, and long-term success.
Financial & Retirement Benefits:
401(k) Safe Harbor Plan with employer match:
Dollar-for-dollar match on the first 1%
50 cents on the dollar up to 6%
Automatic enrolment after 2 months
Equity Participation Share grants subject to board approval, giving you a stake in our mission and long-term growth
Health & Insurance Coverage:
Access to the company's medical insurance with company contributions of up to $1000/month
Access to self-pay vision and dental insurance options
Life Insurance 3x your annual base earnings, employer-paid
Long-Term Disability (LTD) 60% of base salary up to $10,000/month,
Short-Term Disability (STD) 60% of salary up to $2,500/week for up to 13 weeks
Employee Assistance Program (EAP) Full access to our EAP platform including courses and resources to support your wellbeing
Leave & Time Off:
20 vacation days per year
8 sick days
8 paid holidays
Parental Leave
6 weeks fully paid primary caregiver leave
2 weeks fully paid secondary caregiver leave
Holiday Purchase Scheme Buy up to 5 extra vacation days per year
Learning, Development & Culture:
Annual CPD Allowance $1,000 per year for professional development activities relevant to your role
Regular Company Events Including summer and holiday parties, team socials, and more
About Cyted Health
We are redefining digestive health by pioneering non-endoscopic diagnostics, enabling early detection of diseases and access to care for everyone, everywhere.
