Analytical Chemist

synergy

$88K — $105K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Graduate degree in chemistry.
  • 7-10 years of analytical chemistry and R&D experience, specifically within a pharmaceutical setting.
  • Hands-on experience with GC-MS, LC-MS, UPLC, dissolution testing, and TOC instrumentation.
  • Knowledge of GLP/GMP standards and FDA regulations.
  • Experience collaborating with QA/QC teams.

Responsibilities

  • Develop, validate, and optimize analytical methods for pharmaceutical compounds.
  • Operate and troubleshoot analytical instruments like GC-MS and LC-MS.
  • Document procedures and results in compliance with GLP/GMP standards.
  • Analyze data and prepare reports to aid R&D decision-making.
  • Ensure compliance with FDA regulations and internal quality standards.

Benefits

  • Health Care Plan (Medical, Dental & Vision)
  • Paid Time Off (Vacation, Sick, floating & Public Holidays)
  • Training & Development
Full Job Description
As an Analytical Chemist, you will play an important role in generating the analytical insight that supports research and development activities across pharmaceutical programs. This role is focused on producing high-quality laboratory data, strengthening analytical methods, and contributing to cross-functional work that supports technical decision-making and regulatory standards.
Responsibilities
  • Develop, validate, and optimize analytical methods for pharmaceutical compounds and materials.
  • Operate and troubleshoot GC-MS, LC-MS, and related analytical laboratory instruments.
  • Document experimental procedures, results, and deviations in compliance with GLP/GMP standards.
  • Analyze test data and prepare technical reports to support R&D decisions.
  • Ensure laboratory activities meet FDA regulatory requirements and internal quality procedures.

Requirements
  • Graduate degree in chemistry.
  • 7-10 years of analytical chemistry and R&D experience, including experience in a pharmaceutical R&D laboratory.
  • Hands-on experience with GC-MS, LC-MS, UPLC, dissolution testing, and TOC instrumentation.
  • Experience working under GLP/GMP standards and FDA regulatory requirements.
  • Experience interacting and collaborating with QA/QC teams.
  • Experience supporting regulatory and technical reporting across teams.

Benefits
  • Health Care Plan (Medical, Dental & Vision)
  • Paid Time Off (Vacation, Sick, floating & Public Holidays)
  • Training & Development

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