Analytical Chemist

Synergy Bioscience company; Dallas, Northern (TX, KY); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Health care plan

Paid time off

Training & development

Job summary

Synergy Bioscience in Dallas, TX is seeking an Analytical Chemist to generate high-quality laboratory data and strengthen analytical methods across pharmaceutical programs.

You will operate GC-MS, LC-MS, UPLC and related tests, document procedures per GLP/GMP, and contribute to cross-functional regulatory decisions, collaborating with QA/QC teams to prepare regulatory-grade reports.

Qualifications

• Graduate degree in chemistry.
• 7-10 years of analytical chemistry and R&D experience in pharma.
• Hands-on GC-MS, LC-MS, UPLC, dissolution testing, and TOC.
• Experience with GLP/GMP, FDA regulatory requirements, and QA/QC collaboration.

Responsibilities

• Develop, validate, and optimize analytical methods for pharmaceutical compounds and materials.
• Operate and troubleshoot GC-MS, LC-MS, and related instruments.
• Document procedures, results, and deviations per GLP/GMP.
• Analyze test data and prepare technical reports for R&D decisions.
• Ensure activities meet FDA regulatory requirements and internal quality procedures.

Skills

QA/QC collaboration

Regulatory reporting

Cross-functional teamwork

Education

Graduate degree in chemistry

Tools

GC-MS

LC-MS

UPLC

Dissolution testing

TOC instrumentation

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