Manufacturing Operator Vaccines Launch Facility
Leiden (Leiden) Design / Civil engineering / Industrial engineering
Job description
Job Description
Requisition ID: 1805678601W
Department:
The Launch Facility is a state of the art vaccines manufacturing facility which is designed to manufacture drug substance on a 1000 L scale for Phase III and commercial purposes. Currently the facility is in a start-up phase before commercial batches can be produced.
The manufacturing systems are in the end phase of commissioning and qualification phase. Water batches and engineering runs are scheduled for execution. The Operations Team plays a key role in this start up process and delivery of the first vaccine engineering batches by mid-2018.
Additionally, all corresponding production documentation, training records, logistic systems, inventory and all kinds of related activities to make the launch facility ready should be set-up. The final phase is that this Operations Team can execute the vaccine manufacturing process according all EHSS and cGMP regulations.
Job Description:
As (associate) manufacturing operator, you will perform the water batches and engineering runs in the new facility, detects abnormalities and participate in problem solving and implementation of corrective actions. In parallel with these process and manufacturing activities you will be assisting in writing production documentation and training records. And last but not least you will be responsible as area owner for support activities, such as tracking documentation and computer systems, "basic asset care", ensure the cleanliness (5S), maintenance of the area and equipment, sampling, transfer of knowledge etc. to ensure the new launch facility is ready to produce within EHSS and cGMP regulations.
As (associate) Manufacturing Operator, you will be responsible for:
· Taking part in all activities related to the production of cGMP batches in the launch facility. This includes processes such as cell and virus culture, purification processes, formulation & fill and in-process testing.
· Accurately completion of documentation such as batch records, logbooks, etc.
· Working precisely, detecting and solving acute problems and communicate possible abnormalities.
· Preparing, assemble and disassembly of process equipment for production activities.
· Actively participating in setting up documentation to ensure successful production runs.
· Internal organization of the launch facility, including ISL, 5S and kanban systems
Desired profile
Qualifications
Qualifications:
· Associates (MBO) degree in biotechnology, biochemistry, biomedicine, process technology (or equivalent education).
· 1-2 years' experience in a biotechnology or biopharmaceutical industry environment. (associate manufacturing operator)
· 2-4 years' experience in a biotechnology or biopharmaceutical industry environment (manufacturing operator)
· Experience with cGMP environment and EHSS standards is preferred.
Competences:
· High degree of accuracy, initiative.
· Flexible, can deal with changing priorities and stress-resistant.
· Enthusiastic Team player.
· “Can do” attitude, critical and proactive.
· Good communication in Dutch and English, both verbally and in writing.
· Able to work in 16/7 when launch facility is in commercial production.
Primary Location
Netherlands-South Holland-Leiden-
Organization
Janssen Biologics (7266)
Job Function
Production
Requisition ID
1805678601W