Analytical Chemist

synergy; United States; On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Paid Time Off (Vacation, Sick, floatin

& Public Holidays)

Job summary

Synergy Bioscience in Hillsborough, NJ, is seeking an Analytical Chemist to generate analytical insights for pharmaceutical R&D. You will develop robust methods and contribute to regulatory readiness.

The role requires 7–10 years of analytical chemistry and hands-on GC-MS/LC-MS experience, GLP/GMP standards, and collaboration with QA/QC to support regulatory reporting and FDA compliance.

Qualifications

• 7–10 years of analytical chemistry and R&D experience in pharmaceutical labs.
• Experience operating under GLP/GMP standards.
• Experience supporting regulatory and technical reporting.

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.
• Collaborate with QA/QC teams and support regulatory reporting.

Skills

Analytical chemistry

R&D experience

Regulatory knowledge

GLP/GMP knowledge

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.

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.

• Paid Time Off (Vacation, Sick, floating & Public Holidays)

Synergy Consulting LLC offers expert consulting and training services in drug development and regulatory affairs, ensuring optimal strategies for successful pharmaceutical project management.

Pharmaceutical Manufacturing Chemical Manufacturing Manufacturing

Company size 2-10 employees

Company type Self-owned

Momentum

Team growth

Momentum

Team growth

0% in 12 mo

14 employees on LinkedIn

Footprint

Where they work

Headquarters Hillsborough, New Jersey

521 Andria Ave, Hillsborough, New Jersey 08844, US