Independently perform routine testing of process validation samples, raw materials, finished products, and stability samples, while adhering to SOPs and GLPs, and working in a cGMP compliant environment. Analyze and interpret results in written and oral format. Assist Manager in conducting investigations as needed.

Read more: Analytical Chemist

The person would be responsible for making laboratory-sized batches of formulas on the laboratory bench according to formulation guidelines and formulator direction. Also include, but are not limited to filling product, cleaning glassware and sinks, assisting in stability samples, tracking raw materials, and ordering supplies.

Read more: Formulations Associate

Perform downstream production activities in a cGMP manufacturing environment. Assures that operations are conducted in compliance with cGMPs, EP and other regulatory bodies. Coordinates activities with manufacturing staff and other cross functional departments. Overall responsibilities include execution of upstream production processes, employee training, development, quality of product, deviation investigations, productivity improvements, and cost control.

Read more: Manufacturing Technician

The position is a key hire to the Project Management & Client Logistics team and plays a major role in ensuring the company’s adherance to client timelines and budgets. Primarily responsible for overseeing/managing medium or high risk projects for wide range of applications that support global quality systems; spanning multiple functional areas, facilities, and countries which will require the coordination of cross-functional teams.

Read more: Project Manager