CQV Specialist
Mentor Technical GroupPuerto Rico, United States
Posted August 1, 2025
Full Time
About the Company
Mentor Technical Group is a minority-owned business specializing in multidisciplinary compliance, technical, and engineering services for life science and highly regulated industries. With a team of skilled professionals and an ISO 9001 certified Quality System, Mentor offers comprehensive solutions that ensure client confidence, operational efficiency, and risk reduction. The company's commitment to innovation, process integrity, and scalable management methods sets them apart as a trusted partner in the industry.
Job Description
Mentor Technical Group (MTG) is seeking a CQV Specialist to provide technical support and solutions for the FDA-regulated industry. This role involves collaborating with engineers, writing and reviewing C&Q documents, executing commissioning and qualification activities, and ensuring compliance with quality standards. MTG serves life sciences clients globally with offices in Puerto Rico and the United States.
Requirements
- Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Technology, or a related scientific field.
- At least 2 years of experience in GMP manufacturing relevant to the area of expertise.
- Proficiency in English; additional language skills are a plus.
- Strong understanding of regulatory requirements and quality standards.
- Excellent analytical, problem-solving, and communication skills.
- Ability to work collaboratively in a team environment.