Senior Scientist, Analytical Development & QC (NucleicAcids)

Socket.dev

Cambridge (MA)

On-site

USD 126,000 - 182,000

Full time

14 days+
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Job summary

Serif Biomedicines is seeking a Senior Scientist to lead method development, optimization, and qualification for novel nucleic acid therapeutics and LNP delivery systems. You will mentor junior team members and contribute to fast-paced analytical initiatives within a collaborative ADQC group.

You will drive platform development, troubleshoot analytical assays, and communicate findings clearly to cross-functional teams, enabling robust product characterization and regulatory readiness.

Qualifications

  • PhD or equivalent with deep hands-on experience in analytical method development.
  • Experience with nucleic acid cargo and LNP products is required.
  • Proven ability to independently design and troubleshoot complex experiments.
  • Strong communication and mentoring skills.

Responsibilities

  • Lead method development and implementation for nucleic acid cargo and LNP product release, stability and characterization.
  • Lead experimental studies to optimize analytical method performance (specificity, sensitivity, precision, accuracy, linearity).
  • Troubleshoot assay development and instrument issues; act as technical resource for the team.
  • Plan studies, schedule development projects and oversee routine testing across programs.
  • Provide technical input to regulatory filings and author protocols, data, and reports.

Skills

mRNA/LNP expertise
LC-MS
HPLC
Method development
Mentoring
Data presentation

Education

Ph.D. in Chemistry or related field
M.S. in Chemistry/Biochemistry/Engineering
B.S. in Chemistry or related

Tools

Benchling
MS Office
JMP
GraphPad
Empower
Chromeleon

Job description

Serif Biomedicines is seeking a Senior Scientist to lead method development, optimization, and qualification for novel nucleic acid therapeutics and LNP delivery systems. You will mentor junior team members and contribute to fast-paced analytical initiatives within a collaborative ADQC group.

You will drive platform development, troubleshoot analytical assays, and communicate findings clearly to cross-functional teams, enabling robust product characterization and regulatory readiness.

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