synergy

CRDMO offering full product lifecycle services

Analytical Chemist

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours

Full-timeDallas, TX, USANo salary listedIn-person

About the Job

Requirements

A graduate degree in chemistry is required.
Seven to ten years of analytical chemistry and research and development experience, including experience in a pharmaceutical research and development laboratory, is required.
Hands-on experience with gas chromatography–mass spectrometry (GC-MS), liquid chromatography–mass spectrometry (LC-MS), ultra-performance liquid chromatography (UPLC), dissolution testing, and total organic carbon (TOC) instrumentation is required.
Experience working under good laboratory practice (GLP) and good manufacturing practice (GMP) standards and FDA regulatory requirements is required.
Experience interacting and collaborating with quality assurance and quality control (QA/QC) teams is required.
Experience supporting regulatory and technical reporting across teams is required.

Responsibilities

Develop, validate, and optimize analytical methods for pharmaceutical products and materials.
Operate and troubleshoot analytical laboratory instruments.
Document experimental procedures, results, and deviations in compliance with GLP/GMP standards.
Analyze test data and prepare technical reports.
Ensure laboratory activities meet FDA regulatory requirements and internal quality procedures.

Analytical Chemist

Synergy Bioscience Inc · Dallas, United States · Full-time · Posted 2026-09-22

Workplace: on_site

Department: Analytical Chemistry

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 products and materials.
Operate and troubleshoot analytical laboratory instruments.
Document experimental procedures, results, and deviations in compliance with GLP/GMP standards.
Analyze test data and prepare technical reports.
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

Apply

Apply at Synergy Bioscience Inc

About the Company

synergy

CRDMO offering full product lifecycle services

Synergy Bioscience provides CRDMO/CDMO services for pharma, biotech, and medical devices. It supports the product lifecycle with fee-for-service work, including method development and validation, analytical testing, biocompatibility studies, residual solvent analysis, and clinical research to move products from concept to market. The firm differentiates itself by serving small-to-mid-sized companies with cost-effective, high-quality, end-to-end laboratory and regulatory support across USP/EP/ISO standards. Its goal is to be a dependable technical partner that helps clients navigate regulatory requirements and bring products to market.

Company size: 1-10
Company stage: Not listed
Total funding: Not listed
Headquarters: Dallas, TX
Founded: 2016

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