Join Our Team

The Chemist II position responsibilities include both physical and chemical tests on raw materials and finished products according to Current Good Manufacturing Practices (cGMP), United States Pharmacopeia (USP) requirements, the Food and Drug Administration (FDA) and Pharmaceutical Specialties, Inc. Standard Operating and Analytical Procedures.

This position will support activities within the Production Department.

The Sustainable Packaging & EPR Coordinator/Lead will take a lead role in formalizing and expanding an early-stage Extended Producer Responsibility (EPR) compliance program, with a focus on packaging source reduction mandates and packaging qualification activities. This role sits at the intersection of regulatory compliance, sustainability, packaging development, and cross-functional project management. This individual contributor position will partner with Regulatory Affairs, Packaging, Supply Chain, Quality, and Finance to establish the systems, processes, and reporting infrastructure needed to meet all current and emerging packaging and EPR obligations while advancing our broader sustainability goals.

The Microbiology Lab Technician is responsible for conducting quantitative and qualitative analysis of pharmaceutical products, cosmetic products, and ingredients according to the current Good Manufacturing Practices (cGMP) and standard operating procedures.  This position will provide support to the Quality Control Laboratory (QC), Quality Assurance (QA), Research and Development (R&D), and Production (manufacturing and packaging) departments; all working as part of a team.