CQV Specialist

Mentor Technical Group provides technical support and solutions for the FDA-regulated industry. The CQV Specialist will collaborate with engineers to develop commissioning and qualification procedures and documents, and execute commissioning and qualification activities for plants and equipment.

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

Benefits

• Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley
• Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law