Catalent
is a global, high-growth, public company and a leading partner for the
pharmaceutical industry in the development and manufacturing of new
treatments for patients worldwide.
You simply need to submit your resume to each position of interest via UMBCworks by Monday, April 25th for interview consideration.
Most of these positions are in Baltimore or the BWI airport area referred to as Harmans.UMBC INVITATION ONLY HIRING EVENT w/Catalent Pharma Solutions
Manufacturing Associate II (position 9340121)- The Manufacturing Associate II is responsible for supporting the overall GMP upstream or downstream manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing.
Quality Control Technician - Sample Coordinator (position 9340120)- The Quality Control Technician - Sample Coordinator is responsible preparing samples for shipment to contract laboratories as well as POs for shipping of samples. Additionally this role coordinates shipping with our internal team in Materials Control to include preparation of labels and labelling vials for stability samples. This is a great opportunity to gain experience within the biotech industry and to start a career with a growing company!
Central Services Technician- Day Shift (position 9340119)- The Central
Services Technician I will be expected to support the execution of GMP
manufacturing batch records and ensures necessary supply levels in the
manufacturing areas. This role is also responsible for supporting the
overall GMP manufacturing process, through the application of broad
knowledge of theories and principles utilized to solve operational, as
well as routine tasks in the production of bulk products from microbial
and cell culture systems for GMP manufacturing.
QA Specialist (position 9340117)- The Quality Assurance Specialist -Operations (QA OTF) is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product to be used for human consumption. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed.
Manufacturing Associate I (Evergreen)- (position 9340114)- The Manufacturing Associate I performs and documents cGMP activities to support upstream or downstream production areas and operations. This role involves involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed.Manufacturing Associate II (Evergreen)- (position 9340115)- The Manufacturing Associate II is responsible for supporting the overall GMP upstream or downstream manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing.