Associate 2, cGMP Biomanufacturing - Downstream - Catalent
The Manufacturing department is responsible for the execution of clinical and commercial manufacturing in accordance with regulatory, site, and client…
The Manufacturing department is responsible for the execution of clinical and commercial manufacturing in accordance with regulatory, site, and client…
A quality assurance (QA) manager’s primary duty is to maintain appropriate oversight of cGMP processes to ensure the quality of produced pharmaceutical and…
The Tech Services Technician will be expected to support the execution of GMP manufacturing by ensuring stock of gowning inventory and the sterility of…
The Proposal Lead works closely with Business Development (Sales), Project Management and Operations. The Proposal Lead is responsible for project management of…
Experience through hands-on projects that support superior drug development and delivery technologies. Exposure to top-tier scientists and industry leaders.
The Program Manager (PM) will lead multiple client Process Development and GMP Manufacturing projects. The Program Manager is responsible for managing the…
The Project Coordinator will support Project Management teams in the management and successful delivery of assigned Projects. Minimum of a High School Diploma.
The Human Resource Department is responsible for the recruitment management and providing direction for the people who work in the organization through…
A Supply Chain Supervisor will oversee the Client Supply Chain Team and the primary duty is to translate the strategic business portfolio, new and on-going…
Catalent Pharma Solutions is hiring a Quality Assurance Specialist II - Operations who is responsible for supporting operations in a GMP Manufacturing Facility.
The Manufacturing Planner is responsible for the finite manufacturing schedule to support direct manufacturing operations in an efficient and compliant manner.
This Manager, Quality Systems is responsible for management and oversight of the Quality System within the Quality Assurance Unit and effectively hiring,…
The QA Specialist – Raw Materials (Weekend AM) is responsible for providing Quality oversight of QA raw materials across Catalent Maryland sites on Friday,…
The Program Manager (PM) will lead multiple client Process Development and GMP Manufacturing projects. The Program Manager is responsible for managing the…
The training manager’s primary duty is to be a change agent responsible for driving the technical knowledge, skills and attitudes of employee throughout the…
The Procurement Manager is responsible for procurement leadership, sourcing and procuring materials, services and capital for the site.
We are looking for the Senior Accountant who possess solid communication, technology, organizational and analytical skills. CPA, CMA, CFA is strongly preferred.
A Manufacturing Specialist provides direct technical support to operations area as it relates to documentation, equipment procurement, testing, operational…
Validation Specialist position involves designing, executing and concluding qualification studies as they pertain to Installation, Operational and Performance…
The QA Technician - Document Control oversees the revision, issuance and tracking of controlled documents used to support the Phase I/II/III and commercial GMP…