- CQV Project Manager (1)
- CSV Specialist (3)
- Validation Specialist (5)
- Bachelor's Degree in Science or Engineering.
- Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.
- Must be fully bilingual (English / Spanish) with excellent oral skills.
- Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
- Experience with Computer System Validation (CSV), the Computer System Development Life Cycle (SDLC).
- Technical Writing skills.
- Available to work extended hours, possibility of weekends and holidays. START YOUR APPLICATION
MF01-020224 CQV PM - Humacao, Puerto Rico - Validation & Engineering Group, Inc
Descripción
Department: Field - MF Location: Humacao, 069START YOUR APPLICATION
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individuals committed to work under the highest ethics standards for the following positions:
Qualifications: