Website Onesource Consulting
What you’ll do
Performing periodic reviews of cleaning processes at three production departments (Oral Solid Dosages; Liquids, Ointments & Creams; Sterile) to control the validated state.
Coordinating and executing yearly re-qualification studies at the sterile production department.
Providing support to cleaning projects (development & validation). Cleaning methods in scope are
b. Clean In Place
Coordinating the different activities together with validation, production and laboratories:
a. Making appointments with production and laboratories
b. Creation of LIMS requests
c. Execution of studies
d. Evaluation study data results
Providing support to the monitoring program for potential cross contamination of active compounds by sampling non-product contact surfaces per approved protocols.
Bachelor in Chemistry/Biology/Biomedical oriented studies or equivalent through experience.
Pharmacist or Industrial/Chemical Engineer (Process techniques, Chemistry, Biology,..)
What’s in it for you?
Participating during functional meetings that are needed to perform the activities in scope of this assignment.
Working at days when the site is closed is allowed.
Absences from the work station due to holiday, training or other reasons may not hinder the execution of this assignment.
Homework is allowed in exceptional circumstances but may not hinder the execution of this assignment.