Analytical Chemist

synergy; Town of Texas (WI); On-site; USD 85,000 - 135,000; Full time

Benefits offered by this job

Health Care Plan

Paid Time Off

Training & Development

Job summary

Synergy Bioscience in Wisconsin seeks an Analytical Chemist to generate high-quality laboratory data and strengthen analytical methods for pharmaceutical programs. You will contribute to cross-functional work supporting technical decisions and regulatory readiness, with emphasis on GLP/GMP compliance and FDA requirements. The role involves method development, instrument operation, and data reporting.

Qualifications

• Graduate degree in chemistry.
• 7-10 years of analytical chemistry and R&D experience, including pharmaceutical R&D lab experience.
• Experience working under GLP/GMP standards and FDA regulatory requirements.
• Experience with QA/QC teams and regulatory reporting.

Responsibilities

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

Skills

Analytical skills

Data interpretation

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 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.

Qualifications

• 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