Analytical Chemist

synergy; Dallas (TX); On-site; USD 90,000 - 140,000; Full time

Benefits offered by this job

Health Care Plan

Paid Time Off

Training & Development

Job summary

Synergy Bioscience, a pharmaceutical and biotech CRDMO, seeks an Analytical Chemist to generate analytical data and strengthen methods for regulatory-ready development. You will contribute to cross-functional teams and ensure data integrity under GLP/GMP standards.

The role requires a graduate degree in chemistry and 7–10 years of analytical chemistry/R&D experience in a pharmaceutical setting, with hands-on GC-MS, LC-MS, UPLC, and regulatory reporting capabilities.

Qualifications

• Graduate degree in chemistry.
• 7–10 years of analytical chemistry and R&D experience.
• Experience in pharmaceutical R&D laboratory.
• Experience with GLP/GMP standards and FDA requirements.
• Experience interacting with QA/QC teams and regulatory reporting.

Responsibilities

• Develop, validate, and optimize analytical methods for pharmaceutical compounds.
• Operate and troubleshoot GC-MS, LC-MS, and related instruments.
• Document procedures and results in compliance with GLP/GMP standards.
• Analyze data and prepare reports to support R&D decisions.
• Ensure activities meet FDA requirements and internal quality procedures.

Skills

Analytical chemistry

Regulatory compliance

Cross-functional collaboration

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