Analytical Chemist

We are currently supporting a fast growing compounding pharmaceutical organization that is expanding its analytical laboratory capabilities at its Tennessee facility. The organization is bringing dissolution testing and analytical support in-house to support ongoing product development, validation, and GMP release testing activities.

This role will focus on hands-on execution of dissolution testing and analytical laboratory work under the guidance of senior analytical development leadership. The position is ideal for an analytical chemist with early career experience in dissolution testing, HPLC analysis, and GMP laboratory environments who enjoys working in a hands-on laboratory setting.

Responsibilities

• Execute dissolution testing for pharmaceutical products in accordance with established methods and protocols
• Support dissolution method validation activities in alignment with USP <711> and applicable analytical standards
• Perform HPLC or UPLC analysis associated with dissolution samples and stability testing
• Prepare samples, standards, reagents, and mobile phases required for routine analytical testing
• Maintain accurate laboratory documentation in accordance with GMP and data integrity requirements
• Assist with analytical investigations, troubleshooting, and method verification as needed
• Support stability testing and product release testing activities
• Ensure proper operation and routine maintenance of analytical instruments and laboratory equipment
• Work collaboratively with senior analytical chemists and laboratory leadership to meet testing timelines and project deliverables
• Maintain compliance with applicable quality and regulatory standards within the laboratory environment

Requirements:

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or related scientific discipline
• 1–3 years of experience working in an analytical laboratory environment within pharmaceutical, biotech, CRO, or regulated compounding organizations
• Hands-on experience performing dissolution testing is preferred
• Experience operating HPLC or UPLC systems
• Understanding of GMP laboratory practices and documentation requirements
• Strong attention to detail and ability to maintain accurate laboratory records
• Ability to work effectively in a collaborative laboratory environment while supporting analytical development and QC activities

Preferred Experience

• Experience supporting dissolution method validation activities
• Exposure to USP compendial methods and pharmaceutical testing standards
• Experience supporting stability studies and analytical method execution within GMP environments