Analytical Chemist

VPI Compounding•Centennial, CO

12d

About The Position

VPI is a leader in high-quality, specialized pharmaceutical compounding, dedicated to patient safety and therapeutic efficacy. We empower healthcare professionals with innovative, customized medications that meet unique patient needs. This role is essential to our mission, ensuring every product released meets the highest standards of quality and compliance. VPI Compounding is seeking a highly skilled and meticulous Analytical Chemist to join our dedicated Quality team. This critical role is responsible for the integrity, safety, and efficacy of our compounded pharmaceutical products. The successful candidate will perform chemical analyses, lead method development, and drive compliance with rigorous regulatory standards, serving as a pillar of our commitment to quality.

Requirements

Bachelor’s degree in Chemistry, Analytical Chemistry, or a closely related scientific field.
Minimum of 2 years of hands-on experience in an analytical chemistry laboratory, preferably within a pharmaceutical, regulated, or compounding environment.
Proven technical expertise operating and maintaining advanced chromatographic and spectroscopic equipment.
Exceptional attention to detail and ability to execute complex procedures accurately.
Strong verbal and written communication skills to effectively report technical data and findings.
Demonstrated problem-solving abilities in a laboratory setting.
Ability to perform fine motor movements necessary for laboratory work.
Must be able to work at a computer workstation for extended periods.

Nice To Haves

Master’s or PhD highly preferred

Responsibilities

Execute complex qualitative and quantitative analysis of raw materials, in-process samples, and finished pharmaceutical products.
Expertly operate, troubleshoot, and maintain advanced analytical instrumentation, including High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), and UV/Vis spectrophotometry.
Design, develop, and rigorously validate new analytical testing methods for novel and existing pharmaceutical compounds.
Strategically optimize existing testing procedures to significantly enhance laboratory throughput, accuracy, and efficiency.
Implement and strictly uphold quality control procedures in full compliance with FDA regulations, cGMP guidelines , and all internal Standard Operating Procedures (SOPs).
Prepare comprehensive, detailed reports and documentation packages necessary to support regulatory submissions and internal quality audits.
Serve as the key analytical partner to the Formulation Team, providing data-driven insights to support product consistency and innovation.
Maintain a current understanding of advancements in analytical techniques and pharmaceutical compounding to continuously elevate laboratory practices.