This position will act as AQC group leader, responsible for independent problem solving. Execute components of a project. Focus on meeting deliverables Job Responsibilities Supports product development efforts in the process, formulations, and analytical development areas. Conceptualizes and proposes process development, formulations development and analytical development

KBI Leuven is working on many different projects and is searching for a QA/QP Specialist to join their ambitious small sized team located in Leuven, Belgium. Responsibilities Under the direction of the Head QA Leuven site, the QA/QP Specialist will be responsible for Performing the Qualified Person (QP) function as regards Batch certification, as defined by Directive 2001/

The incumbent will support GMP manufacturing operations for late phase and commercial mammalian Cell Culture programs and oversee compliance activities for the department. The individual will support operations during the planning stages by releasing electronic manufacturing logbooks and records, as needed. The employee will support operations during the execution stage b

The downstream manufacturing supervisor will lead associates during the startup and production in the purification areas for a new clinical GMP biopharmaceutical facility. The supervisor will coach associates during the commissioning, qualification, and production activities while safeguarding work environments and ensuring cGMP compliant behaviors. Downstream supervisors

The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. This person is responsible for the

This position is on a 2 2 3 shift, 7a 7p. The Manufacturing Associate I/II Downstream is responsible for the execution of production activities for early and late phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II Downstream must follow the instructions depicted in SR's, EPR's, BR's, SOP's and forms. Additionally, must ensure all work i

This position is on 2 2 3 shifts, 7a 7p. The Sr. Manufacturing Associate I/II MFG Support is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Sr. Manufacturing Associate I/II Support must follow the instructions depicted in SR's (Media / Buffer Solution Records), SOP's and forms. Additionally, must ensure

This position is on 2 2 3 shifts, 7p 7a. The Sr. Manufacturing Associate I/II MFG Support is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Sr. Manufacturing Associate I/II Support must follow the instructions depicted in SR's (Media / Buffer Solution Records), SOP's and forms. Additionally, must ensure