Analytical Scientist I

Quotient Sciences•Concord Township, PA

20h•Onsite

About The Position

Quotient Sciences is seeking a motivated and detail‑oriented Analytical Scientist I/II to join our Translational Pharmaceutics (USTP) and Early Phase Clinical Trial Material (CTM) teams. This cross‑functional role offers the opportunity to work at the forefront of drug development, supporting both release and stability testing of clinical trial materials within a fast‑paced, collaborative quality control environment. As an Analytical Scientist, you will perform hands‑on laboratory testing, operate a wide range of analytical instrumentation, and contribute directly to the timely delivery of high‑quality data essential to progressing clinical programs. This position is ideal for someone who thrives in a dynamic setting, values scientific rigor, and is committed to maintaining the highest standards of GMP compliance and laboratory safety.

Requirements

Bachelor’s degree in Chemistry or other related field of study required
Experience in an Industrial Pharmaceutical Laboratory (0-3 years)
Knowledge of federal and state regulations and guidelines including FDA, EPA, OSHA, and DEA
Remains in compliance with all company and site policies and procedures
Knowledge of laboratory safety procedures, precautionary laboratory measures, and GMP procedures
Competency in Microsoft Office required
Competency in experiment documentation and basic laboratory skills
Use instruments, equipment, and technology safely and effectively
Able to work in a hazardous environment with a high requirement to follow safety procedures
Working knowledge of HPLC and dissolution
Working knowledge of Chromatographic data systems (CDS) such as Empower
Good communication skills with the ability to effectively document testing process and report information to supervisor
Good time management skills with the ability to ensure accurate and timely data reports
Good writing skills with the ability to document and explain findings
Good analytical skills with the ability to document findings
Ability to work independently and efficiently on critical, time sensitive projects
Commitment to continuous education to remain in current profession and industry trends, make suggestions for new improvements, and learn new skills, procedures, and aspects of formulation and development

Responsibilities

Operates and troubleshoots the following instruments and equipment to test and evaluate pharmaceutical samples
HPLC/UPLC, dissolution apparatus, Karl-Fischer water content titrator, GC, FTIR, UV, and any other instruments as directed
Follows analytical testing methods, compendial methods, experimental procedures, and SOPs
Conducts release and stability testing for drug product in the QC laboratories
Documents test results in traditional or electronic laboratory notebook (ELN), in real time, and communicates status of test results to supervisor
Peer reviews laboratory notebooks or ELN documentation for technical details
Maintains control of all project-related pharmaceutical samples submitted to the laboratory as they can contain potent and/or hazardous components
Performs cleaning and housekeeping duties to ensure the laboratory is continuously maintained in a safe and orderly condition
Supports testing and compiling of data for department LIRs, Deviations, CAPAs, Change Controls under the direction of the supervisor
Trains on all SOPs and company procedures and remains current with training curriculum
Translational Pharmaceutics: complete testing and release activities on final product for delivery to clinic
Quickly turnaround testing and results to meet timelines