Lead Analytical Scientist – API & Peptide Development

Veranova

Harvard (MA)

On-site

USD 140,000 - 155,000

Full time

10 days ago

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Benefits offered by this job

Health & Wellness benefits
401(k) with company match

Job summary

Veranova, a global leader in APIs, seeks a Principal Scientist-Analytical Research & Development to lead development and validation of analytical methods for APIs and peptides. You will work on HPLC/UPLC, LC-MS, NMR, and other techniques, ensuring GMP compliance and readiness for regulatory audits.

The role involves hands-on lab work, collaboration with project teams, and technical leadership across development programs.

Qualifications

  • PhD or MS with GMP experience in analytics.
  • 8+ years in GMP environment for APIs and analytical method development.
  • 3+ years in oligonucleotides and/or peptides.
  • Experience with HPLC/UPLC, GC, NMR, UV, FTIR, XRPD, LC-MS, GC-MS, ICP-MS.

Responsibilities

  • Lead design, development, and execution of analytical methods per ICH and Health Authority guidelines.
  • Perform release and stability testing for materials, intermediates, and APIs.
  • Author and review method qualification/validation/transfer protocols and reports.
  • Prepare and review scientific reports for internal and external entities.
  • Maintain and troubleshoot analytical instrumentation.
  • Act as technical contact for clients, providing updates and solving challenges in real time.
  • Support audit readiness and participate in quality audits (FDA, regulators).
  • Ensure compliance with GMP, DEA, FDA, and related regulations.

Skills

Analytical Chemistry
GMP Experience
Method Development
Oligonucleotides/Peptides
HPLC/UPLC

Education

PhD in Analytical Chemistry
MS in Analytical Chemistry

Tools

LC-MS
NMR
GC
ICP-MS

Job description

Veranova, a global leader in APIs, seeks a Principal Scientist-Analytical Research & Development to lead development and validation of analytical methods for APIs and peptides. You will work on HPLC/UPLC, LC-MS, NMR, and other techniques, ensuring GMP compliance and readiness for regulatory audits.

The role involves hands-on lab work, collaboration with project teams, and technical leadership across development programs.

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