Associate Principal Scientist, Synthetic Purification Ar&d

Merck Merck · Pharma · NJ

The Associate Principal Scientist will focus on chromatographic isolation of pharmaceutical API and impurities from analytical scale to semi-prep scale and prep scale, supporting various pharmaceutical modalities. This role involves partnering with process chemists and analytical scientists to deploy efficient chemical isolation methods and establish innovative purification workflows.

What you'd actually do

  1. chromatographic isolation of pharmaceutical API and impurities from analytical scale to semi-prep scale and prep scale, covering the space of small molecules, peptides, conjugate-based modalities as well as emerging modalities in our portfolio.
  2. partner with process chemists and analytical scientists to deploy efficient and fit-for-purpose chemical isolation methods, to establish innovative purification workflows, and to deliver high purity materials.
  3. Creative problem solving in scientific research and development, with proven track-record of translating R&D problem solving into impactful pipeline deliveries.
  4. Experience in mentoring peers.
  5. External scientific engagement that may include a combination of publications, industry white paper contributions, presentations at scientific meetings.

Skills

Required

  • Accountability
  • Adaptability
  • Analytical Method Development
  • Antibody Drug Conjugates (ADC)
  • Antibody Therapeutics
  • Assay Development
  • Biological Assay Development
  • Biopharmaceutical Industry
  • Biopharmaceuticals
  • Biopharmaceutics
  • Cell-Based Assays
  • Chromatographic Techniques
  • Column Chromatography
  • Communication
  • Cross-Functional Teamwork
  • External Collaboration
  • GMP Compliance
  • High Resolution Mass Spectrometry (HRMS)
  • Liquid Chromatography-Mass Spectrometry (LC-MS)
  • Manufacturing
  • Mass Spectrometry (MS)
  • Mass Spectrometry Analysis
  • Mentorship
  • Optimism

Nice to have

  • Pharmaceutical GMP experience
  • Hands-on experience using Teledyne ISCO-MS systems

What the JD emphasized

  • Ph.D. in Chemistry or a related field with a minimum of 5 years of experience in biopharmaceutical industry.
  • M.S. with a minimum of 8 years of experience in the Biopharmaceutical industry
  • Bachelor’s with a minimum of 12 years of experience in the Biopharmaceutical industry.
  • Expertise in analytical, semi-prep/prep scale chromatography (RPLC, NPLC, SFC), technologies, instrumentation, and workflows, with demonstrated experience in its applications in chiral, achiral isolation of challenging pharmaceutical mixtures to support a variety of pharmaceutical modalities including small molecules, peptides, antibody-drug conjugates and vaccines adjuvants etc.
  • Experience in mass spectrometry and its application in MS-directed chromatographic purification.
  • Working knowledge of orthogonal detection technologies, including PDA, Multi-angle light scattering, charged aerosol detection _etc._
  • Creative problem solving in scientific research and development, with proven track-record of translating R&D problem solving into impactful pipeline deliveries.
  • Experience in mentoring peers.
  • External scientific engagement that may include a combination of publications, industry white paper contributions, presentations at scientific meetings.
  • Pharmaceutical GMP experience is highly preferred.