13 jobs voor Process Engineer Biotech gevonden in Zwijnaarde (9052)

.Lead and supervise various units within the process, such as component preparation, production support activities, process, filling & finishing, and cryopreservation..

Lead and supervise various units within the process, such as component preparation, production support activities, process, filling & finishing, and cryopreservation..Build strong collaborative relationships with various departments, including Manufacturing Operations, QC IPC Operations, Quality, Facilities & Engineering, MS&T/Manufacturing Excellence, Training, Planning, Procurement & Supply Chain/Warehouse..

Component preparation manufacturing, manufacturing support operations, process, fill & finish and cryopreservation) according to standard operating procedures and batch records and ensure safe and compliant manufacturing operations according to c.GMP requirements..

Component preparation manufacturing, manufacturing support operations, process, fill & finish and cryopreservation) according to standard operating procedures and batch records and ensure safe and compliant manufacturing operations according to c.GMP requirements..

Onze klant, een biotech bedrijf, gevestigd in Zwijnaarde, is een wereldwijd biotechnologiebedrijf dat de innovatieve CAR T celtheraptie naar Gent brengt.Het bedrijf maakt hiermee dagdagelijks het verschil in het leven van vele patiënten die lijden aan kanker en andere levensbedreigende ziektes..

GMP facility to manufacture products..Conduct analytical testing of raw material/utility, in process, or final product samples submitted to the QC laboratories..

Planning van operators voor verschillende stappen binnen het CAR T proces..Tijdig uurroosters opmaken.

.Establish key stakeholder relationships with internal stakeholders (Manufacturing Operations, QC IPC Operations, Quality, Facilities & Engineering, MS&T/Manufacturing Excellence, Planning).

GMP facility to manufacture products..Conduct analytical testing of raw material/utility, in process, or final product samples submitted to the QC laboratories..

GMP compliance..Build partnerships with cross functional teams, addressing production issues..Assist in investigations and personnel training..Lead daily shift meetings, assign tasks, and collaborate for personnel development..

Lead daily shift meetings, assign tasks, and collaborate for personnel development..Ensure safe and compliant manufacturing operations within a team environment..Lead CAR T process units, ensuring SOP and c.GMP compliance..

Executing aseptic manual processes for clinical and commercial grade ATMPs, including cell isolation, selection, activation, transduction, culture, fill & finish, and cryopreservation, while maintaining Good Documentation Practices (GDP)..Working in a cleanroom environment (Grade A/B/C/D) to guide and perform production tasks, ensuring adherence to safety policies and quality systems..

Executing aseptic manual processes for clinical and commercial grade ATMPs, including cell isolation, selection, activation, transduction, culture, fill & finish, and cryopreservation, while maintaining Good Documentation Practices (GDP)..Working in a cleanroom environment (Grade A/B/C/D) to guide and perform production tasks, ensuring adherence to safety policies and quality systems..