Analytical Chemist

Synergy Bioscience, Inc.; Dallas (TX); On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Health Care Plan (Medical, Dental &amp

Job summary

Synergy Bioscience is seeking a senior analytical chemist to lead method development and validation for pharmaceutical compounds. You will design, optimize, and troubleshoot GC-MS, LC-MS, UPLC, and TOC workflows, ensuring data integrity under GLP/GMP and FDA requirements.

You will document procedures, analyze test data, and prepare regulatory and technical reports while collaborating with QA/QC teams to support R&D decisions and regulatory readiness.

Qualifications

• Graduate degree in chemistry.
• 7-10 years analytical chemistry and R&D experience in pharma R&D.
• Hands-on GC-MS, LC-MS, UPLC, dissolution testing and TOC instruments.
• Experience with GLP/GMP standards and FDA regulatory requirements.
• Experience collaborating with QA/QC teams.
• Experience supporting regulatory and technical reporting across teams.

Responsibilities

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

Skills

Analytical chemistry expertise

QA/QC collaboration

Regulatory reporting

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.

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