Validation Scientist II at Alliant lab consulting
United States, , USA -
Full Time


Start Date

Immediate

Expiry Date

07 Nov, 25

Salary

96942.65

Posted On

09 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Molecular Biology, Flexible Schedule, Documentation, Biology, Communication Skills, Collaboration

Industry

Hospital/Health Care

Description

VALIDATION SCIENTIST II

Location: Remote (Up to 50% travel within the continental U.S.) Job Type: Full-Time Industry: Molecular Diagnostics / Clinical Laboratory Services

JOB SUMMARY

Alliant is hiring a Validation Scientist II to support clinical laboratory validations for FDA-approved and laboratory-developed tests. This remote role involves hands-on molecular diagnostics, client training, and project leadership. Ideal candidates are experienced in qPCR, NGS, and clinical lab workflows, and thrive in dynamic, collaborative environments.

QUALIFICATIONS

  • MB(ASCP) or MDT(AMT) certification preferred
  • Master’s degree in biology, molecular biology, or related field preferred
  • 3+ years of experience in a molecular diagnostics lab
  • Experience with QuantStudio, Bio-Rad CFX, and Illumina platforms preferred
  • Strong written and verbal communication skills
  • Ability to lift up to 30 lbs and travel up to 50%
  • Comfortable working remotely and independently

SKILLS & COMPETENCIES

  • Strong attention to detail and documentation
  • Excellent troubleshooting and problem-solving skills
  • Team-oriented with clear communication
  • Adaptable to changing priorities and fast-paced environments
    Benefits: Competitive compensation, remote flexibility, travel opportunities, and the chance to contribute to cutting-edge diagnostic solutions.
    Apply Today: Join a team that values precision, collaboration, and innovation.
    Job Type: Full-time
    Pay: $80,497.02 - $96,942.65 per year

Benefits:

  • Flexible schedule

Schedule:

  • 8 hour shift

Work Location: On the roa

How To Apply:

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Responsibilities
  • Perform validations for FDA IVD and LDT assays
  • Train client-site technical staff and document training activities
  • Conduct nucleic acid extraction, qPCR, and NGS
  • Process high-volume samples using manual and automated methods
  • Maintain equipment and perform QC/QA with accurate documentation
  • Troubleshoot assays and collaborate with team leads
  • Draft SOPs, validation reports, and lab documentation
  • Lead offsite projects and guide follow-up experiments
  • Attend daily virtual meetings and provide project updates
  • Communicate professionally with internal teams and clients
  • Follow OSHA, HIPAA, and safety protocols
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