QUALITY CONSULTING GROUP, a leader inthe pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Provides the technical validation engineering support of process and/or equipment upgrades, replacements, and modifications in the laboratory, manufacturing or manufacturing support environment.
• Employ advanced validation engineering techniques and/or modifications of advanced techniques within area of validation engineering expertise.
• Advanced validation knowledge (equipment qualification, cleaning, sterilization).
• Applies extensive technical validation expertise, and has full knowledge of other related disciplines.
• Work with manufacturing, process development, utilities, facilities, labs, and/or quality assurance in developing requirements and recommendations for large and/or highly complex process, system/facility modifications.

Qualifications:

• Bachelor Degree
• Five (5) years of previous experience
• Validation expertise
• Sterilization, Autoclaves, Isolators & Depyrogenation
• Kaye Validator & Data loggers
• Equipment Qualification
• Equipment Re-qualification