Analytical Chemist

Synergy Bioscience, Inc.; Dallas (TX); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Health Care Plan (Medical, Dental &amp

Job summary

Synergy Bioscience, Inc. is seeking a seasoned analytical chemist to develop and validate methods for pharmaceutical products. The role requires leading method development, instrument troubleshooting, and ensuring GLP/GMP and FDA alignment across QA/QC.

Collaboration with cross-functional teams to support regulatory filings is essential. Ideal candidates hold a graduate degree in chemistry with 7–10 years of pharma R&D experience, and hands-on GC-MS/LC-MS, UPLC, and dissolution/TOC expertise in

Qualifications

• 7–10 years in analytical chemistry and R&D, including pharma R&D lab experience.
• 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 and supporting regulatory reporting.

Responsibilities

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

Skills

Analytical Chemistry

Method Validation

GC-MS / LC-MS

FDA/GLP/GMP

Education

Graduate degree in chemistry

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 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