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QUALITY CONSULTING GROUP, a leader in the 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:

+ Developing, executing, and documenting validation protocols, deviations, and reports to meet company and regulatory requirements.

+ Collaboration with cross-functional teams—including Quality, Manufacturing, and Maintenance—to plan, coordinate, and execute validation activities while ensuring efficient use of time and resources.

+ Maintain accurate records, adhere to safety guidelines during validations, and support investigations or issue resolution related to validation activities.

Qualifications:

+ Bachelor’s degree

+ 2 years of relevant experience

+ Experience in generation and execution of equipment validation.

+ Hands-on experience with equipment and process validation in a regulated industry.

+ Basic knowledge of statistical tools which are used for sampling determination, and process characterization.

+ Proven ability to manage validation documentation and meet deadlines.

+ Shift: 1st shift

Quality Consulting Group, LLC 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.

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