Molecular Technologist

Cyted HealthAtlanta, GA
1dOnsite

About The Position

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. 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.

Requirements

  • 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
  • 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

Nice To Haves

  • Experience translating manual molecular processes to semi-automated or automated platforms (advantageous)

Responsibilities

  • 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
  • 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
  • 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

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
  • 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
  • 20 vacation days per year
  • 8 sick days
  • 8 paid holidays
  • 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
  • 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
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