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:

+ Support product transfer activities, mainly focus on process validation and release product up to commercial release.

+ Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under appropriate federal regulations.

+ Coordinates activities with clients, programmers/developers and operating personnel, domestic and, as appropriate, global.

+ Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation and ma...