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Analytical Chemist

synergyDallas, Texas🇺🇸United StatesPosted Sep 22, 2026

Why This Role Stands Out

This Analytical Chemist role at Synergy Bioscience offers a fantastic opportunity to significantly contribute to groundbreaking pharmaceutical development and advance your expertise in method validation and advanced instrumentation. You'll thrive here if you possess a strong background in analytical chemistry, GLP/GMP, and a passion for producing high-quality data within a reputable CRDMO. Apply now to join a dynamic team dedicated to scientific rigor and innovation.

Quick Overview

Seniority
Mid Senior
Employment type
Full Time
Work mode
On Site
Location
Dallas, Texas, United States
Posted
12 hours ago
Compliance

Job Description

Synergy Bioscience is a pharmaceutical and biotech CRDMO providing research, development, manufacturing, testing, and regulatory consulting services. Our work supports the advancement of pharmaceutical products from early research through quality-focused development and regulatory readiness, with a strong emphasis on scientific rigor, compliance, and reliable laboratory execution.

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

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