Pharma Universe is a leading organization in the pharmaceutical industry, specializing in the manufacturing of biologics. With a focus on producing high-quality drug substances, the company is currently expanding its operations in Chicago to accommodate increased production demands. The company emphasizes compliance with cGMP standards and promotes a culture of safety and efficiency in its manufacturing processes. Pharma Universe is committed to the development and training of its personnel, ensuring that they are equipped with the necessary skills and knowledge to excel in their roles. The organization values collaboration and continuous improvement, striving to deliver innovative solutions in the pharmaceutical sector.
The Maintenance Mechanic position offers a chance to work collaboratively while maintaining and repairing production equipment and facility systems.
We are seeking Manufacturing Scientists to support the scaling of production in our new facility in New Jersey.
A Senior Data Engineer to design and develop a centralized Data Warehouse infrastructure focusing on scalable data solutions.
The Senior Manager of Manufacturing will oversee biologics manufacturing operations, focusing on process optimization and compliance.
A Performance Engineer to ensure optimal performance, testing, and observability within a product domain.
Seeking a Director of Manufacturing Operations to lead and optimize manufacturing processes in a chemical manufacturing environment.
Join as a Manufacturing Operator to ensure high-quality pharmaceutical production.
The USP Bioprocessing Specialist III will perform upstream manufacturing and ensure compliance with cGMP regulations in a state-of-the-art facility in New Jersey.
The Manufacturing Quality Specialist ensures compliance with cGMP regulations and supports manufacturing operations through quality oversight and documentation review.
The Manufacturing Quality Specialist ensures compliance with cGMP regulations and supports manufacturing operations through quality oversight and documentation review.
The Downstream Manufacturing Scientist will optimize and execute downstream processing in a state-of-the-art facility while adhering to cGMP regulations.
The Downstream Manufacturing Scientist will optimize and execute downstream processing in a state-of-the-art facility while adhering to cGMP regulations.
Join the Quality Control team as a Chemist II/III, performing analytical testing in a GMP/GLP-regulated environment.
The Upstream/Downstream Manufacturing Supervisor oversees production activities for Biologics Manufacturing, ensuring compliance and quality in drug substance production.
Seeking dynamic Upstream Manufacturing Scientists to lead mammalian cell culture and bioreactor operations in a cGMP environment.