VIVEbiotech is looking for a Production Technician to fill this key position reporting directly to the Production Responsible. You will execute lentiviral vector production processes according to the instructions of the manufacturing guides under the GMP regulations. To do this, you will be part of a team that will propose improvements, write manufacturing protocols, standard work procedures (SOPs) and other relevant documents related to manufacturing.
Description:
- Execute Lentiviral vectors manufacturing processes according to GMP manufacturing guides.
- Drafting of manufacturing protocols, standardized operating procedures (SOPs) and other relevant manufacturing guides. Comply with and ensure compliance with internal manufacturing standards.
- Be part of a multidisciplinary team to carry out process optimizations and researches.
- Carry out maintenance of manufacturing areas to guarantee their status and compliance with GMP regulations.
If you are interested, please send your CV to personas@vivebiotech.com
About VIVEbiotech:
VIVEbiotech is a Contract Development and Manufacturing Organization (CDMO) with over 20 biotech companies worldwide that have placed their trust in them. They develop and manufacture lentiviral vectors as a European leader working under both EMA and FDA standards. The lentiviral vectors produced by VIVEbiotech are used to treat a range of disorders, including haematological and solid cancers, and rare diseases. They are looking for you to be part of their Team!
VIVEbiotech
Lentiviral vectors, Lentivirus, Gene therapy, Gene-Modified Cell Therapy, Advanced Therapies, Regenrative Medicine, Tailor-made.
