Description
For one of our clients in the pharmaceutical industry, we are currentlylooking for a QA Formulation consultant
Start: ASAP
Length: 6 months with a possibility of extension
Location: South of Brussels
KEY RESPONSIBILITIES:
* Ensure (cumulatively or not):
(A) deviations, complaints, change controls, CAPA, are reviewedand handle it in a timely manner with the right quality oversight
(B) batches of the intermediate product related to the area ofresponsibility are released in a timely manner
(C) quality oversight of validation activities
* Adequately and timely escalated critical topics to higher management
* Represents QA in all operational meetings related to the area ofresponsibility
PREREQUISITES:
Education: University Degree or equivalent
Specific skills:
* Good understanding of:
o Current Good Manufacturing practice (cGMP)
o Supply Chain processes
o Manufacturing
* Good interpersonal relationship
Knowledge:
* Management skills: Deviation management, CAPA management, Complaintsmanagement
* Experience: Release and/or validation
Expence:
* At least 2 years in a QA role (!)
o within a pharmaceutical industry, preferably in a sterilemanufacturing company
o (+) 3 years in production/QA role
* Experience of cGMP
* Experience within aseptic facility