JT635 - ENGINEERING SPEC

Villalba, Puerto Rico

Temporary

Medical Devices

Mid Level

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:

Analyses and solves complex engineering problems, proposing and implementing innovative solutions.
Reviews and interpret engineering designs, drawings, and specifications to ensure accurate execution and compliance with relevant standards.
Lead and support process development and optimization efforts, working closely with manufacturing and design teams.
Maintain detailed records of design specifications, changes, test results, and validation processes.
Support the creation and implementation of engineering documentation, including process flows, technical reports, and manuals.
Work closely with other engineering teams, product managers, and business leaders to ensure alignment on project goals and technical requirements.

Qualifications:

Bachelor’s degree in Engineering
Minimum of 2 years of relevant experience
Knowledge of Injection Molding Process and Tooling
Knowledge of Process Validation Lifecycle (from Installation qualification, TMV, process characterization, operational qualification to performance qualification, PFMEA).
Knowledge on drawings interpretation
Available to work 1st and 2nd shifts
Training 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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