Inteldot has over 15 years in the life sciences industry, with operations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Employment type: Full time and onsite role
Role Summary
The C&Q Specialist is responsible for supporting and executing commissioning and qualification activities for capital projects within a regulated pharmaceutical manufacturing environment. This role ensures that equipment, systems, and facilities are installed, tested, and verified in compliance with GMP, regulatory requirements, and company standards. The C&Q Specialist develops and executes protocols, supports equipment testing, documents results, and ensures data integrity throughout all commissioning and qualification activities.