Lead Analytical Development Scientist — RNA & Microbiome

Meet Life Sciences Ltd.

Watertown (MA)

On-site

USD 120,000 - 150,000

Full time

12 hours ago
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Job summary

Meet Life Sciences Ltd. in Watertown, MA, seeks an Analytical Development Scientist (Scientist III) to lead analytical method development, optimisation and qualification for RNA, DNA and microbiome platforms.

The role offers technical ownership in a fast-paced, collaborative environment. You will design phase-appropriate studies, support method transfers in a cGMP context, troubleshoot challenges, and document findings, collaborating with cross-functional teams to advance cutting-edge nucleic

Qualifications

  • PhD in Biosciences or related field with 2+ years in industry OR
  • Master's degree with 5+ years in industry OR
  • Bachelor's degree with 8+ years in industry.

Responsibilities

  • Lead development, optimisation and qualification of analytical methodologies for RNA, plasmid DNA and microbiome platforms.
  • Design and execute phase-appropriate analytical studies, method qualification and sample testing.
  • Support analytical method transfer and development in a cGMP environment.
  • Troubleshoot complex technical challenges, analyse data and document results.
  • Collaborate with cross-functional teams to support project milestones and technical deliverables.
  • Identify opportunities to improve analytical processes and introduce innovative technologies.
  • Act as a technical subject matter expert supporting internal and external projects.

Skills

Analytical method development
Experimental design
Troubleshooting
Cross-functional collaboration
Documentation

Education

PhD in Biosciences or related
Master's degree
Bachelor's degree

Job description

Meet Life Sciences Ltd. in Watertown, MA, seeks an Analytical Development Scientist (Scientist III) to lead analytical method development, optimisation and qualification for RNA, DNA and microbiome platforms.

The role offers technical ownership in a fast-paced, collaborative environment. You will design phase-appropriate studies, support method transfers in a cGMP context, troubleshoot challenges, and document findings, collaborating with cross-functional teams to advance cutting-edge nucleic

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