Inteldot has over 14 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.

Description:

Under general direction, candidate must execute functions as the Quality Control Specialist for Laboratory Analytical Assets.

Essential Requirements:

Experience with Laboratory Analytical AssetsGMP Documentation Computerized Maintenance (Asset / PM creation, Documentation, etc.)Technical Documentation skills

Responsibilities:

Responsible for providing technical guidance in the laboratory operations.Provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. Resolve technical issues and troubleshoot as necessary, Ensure laboratory compliance, which includes implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies, Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact.

Education:

Master's degree and 3 years of directly related experience or bachelor's degree and 5 years of directly related experience or associate's degree and 10 years of directly related experience or High school diploma / GED and 12 years of directly related experience.