Job Description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities: 

+ Perform and/or review process validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV] (not laboratory).

+ Experience in production line.

+ Basic knowledge in defining validation strategies (e.g. requirements flow down from design to manufacturing).

+ Experience with Risk Management documentation: pFMEAs.

+ Basic knowledge in statistics (preferably using Minitab).

+ Experience with projects: design requirements validation, manufacturing controls (not Operational Excellence).

Qualifications:

+ Bachel...

Apply for this Position

Ready to join Quality Consulting Group? Click the button below to submit your application.

Submit Application