Senior Scientist, Biophysical Characterization for Biologics

Merck & Co.

Rahway (NJ)

On-site

USD 117,000 - 184,000

Full time

6 days ago
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Benefits offered by this job

Medical, dental, vision
401(k) retirement plan
Paid holidays
Vacation and sick days

Job summary

Merck & Co., Inc. in Rahway, NJ, seeks a Senior Scientist in Biophysics to advance biotherapeutics characterization and develop analytical tools for CMC development.

You will work with formulation, process, and device groups to ensure robust drug substances and products, across a collaborative, growth‑oriented environment. You will author technical/regulatory documents, present data, and manage projects, with opportunities to publish findings and engage with scientific societies.

Qualifications

  • Experience in analysis of biologics, protein/peptide stability, interactions.
  • Hands-on biophysical characterization of proteins/peptides.
  • Understanding of protein aggregation mechanisms.
  • Ability to deliver with tight timelines.
  • Strong initiative, creativity and problem solving.
  • Excellent written and oral communication; cross-functional work.

Responsibilities

  • Develop and implement biophysical/particle characterization tools for biotherapeutics.
  • Collaborate with process, formulation and device teams within CMC development.
  • Author technical reports and regulatory documents; present data.
  • Manage projects and contribute to independent research and publications.

Skills

Biophysics
Biologics analysis
Protein characterization
Oral/written communication
Team collaboration
Independent work

Education

Ph.D. in Biophysics/related
MS in Biophysics/related with 4-8 years

Tools

CD
IR
DSC
AUC
DLS

Job description

Merck & Co., Inc. in Rahway, NJ, seeks a Senior Scientist in Biophysics to advance biotherapeutics characterization and develop analytical tools for CMC development.

You will work with formulation, process, and device groups to ensure robust drug substances and products, across a collaborative, growth‑oriented environment. You will author technical/regulatory documents, present data, and manage projects, with opportunities to publish findings and engage with scientific societies.

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