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Chemistry 🏢 Full Time ⭐️ Verified

Senior Analytical Chemist

NovaChem Analytics
Cambridge, MA
Salary Estimate
USD 110.000 – USD 150.000
Posting Time
7 Mei 2026
Deadline
7 Mei 2027

Job description

NovaChem Analytics is seeking a results-driven Senior Analytical Chemist to join our Cambridge team. You will lead method development and validation for pharmaceutical-grade analyses that support drug discovery and quality control. This role combines hands-on analytical work with cross-functional collaboration to drive scientific excellence.

As a key member of our R&D group, you will design robust experiments, optimize chromatographic and spectrometric approaches, and ensure data integrity under GLP/GMP standards. We offer competitive compensation, comprehensive benefits, and opportunities for career growth in a fast-growing biotech environment.

Location: Cambridge, MA; on-site collaboration with manufacturing and QA teams.

Responsibility

  • Lead development and optimization of HPLC, LC-MS/MS, and GC-MS methods for release testing and stability studies.
  • Design validation protocols, execute method validation per ICH guidelines, and maintain technical documentation.
  • Interpret analytical data, prepare technical reports, and present findings to cross functional teams.
  • Troubleshoot instrumentation and implement continuous improvement initiatives for analytical platforms.
  • Ensure compliance with GLP and GMP standards, ISO 17025 awareness, and company SOPs; oversee method transfer to QC laboratories.
  • Mentor junior scientists and provide training on analytical techniques and data analysis.
  • Collaborate with R&D, QC, and external CROs to support scale up and product development.

Qualification

  • PhD in Analytical Chemistry, Chemistry, or related field; or MS with 5+ years of relevant experience.
  • Strong expertise in HPLC, LC-MS/MS, GC-MS, and NMR; experience with method development and validation.
  • Proficient in data analysis software and statistical interpretation; ability to troubleshoot complex datasets.
  • Experience in GLP GMP environments and ISO 17025; familiarity with regulatory guidelines (ICH, USP).
  • Excellent problem solving, communication, and technical writing skills.
  • Ability to manage multiple projects, prioritize tasks, and work cross functionally in a fast paced environment.
  • Commitment to safety, quality, and continuous improvement.

Required Skills

HPLC LC-MS/MS GC-MS NMR method development method validation data analysis GMP/GLP ISO 17025 SOPs experimental design instrumentation maintenance

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