Description
Job Responsibilties:- work on special projects with mininal supervision
- write, review change controls/sops and revise sops
- proactively suggest department improvements
- represt QA at meetings: inc prepare and distribution of batch records, along with associated records
- investigate and prepare reports for process deviations, failures, complaints and CAPA's
- assist in training
- sampling
- execute environmental monitoring protocols
- assist with fda and customer audits
- sample raw materials as required
- alternate shift patterns
Your cv will need to include:
- prior experience reviewing manufacturing and/or laboratory investigations froma compliance standpoint
- experience writing manufacturing and/or laboratory investigations
- experience conducting internal and external audits
- experience working in department responsible for assigning and assesing the effectiveness of CAPA's
If this positions sounds like a match with your previous career and qualifications then please get in contact by submitting your cv or alternatively calling Andy .
Thanks for reading.