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:

1. Manufacturing processes, products and builds knowledge
2. Process Validation Lifecylce ( from Installation qualification, TMV, process characterization, operational qualification to performance qualification, PFMEA)
3. Basic knowledge on drawings interpretation

Qualifications:

- Bachelor’s degree in Engineering
- 3 years' of experience.

The candidate will be working on the introduction on a new product that may include:

- Process Development and documentation
- Equipment validation
- SOP Development
- Line layout and infrastructure and development
- MES (Manufacturing Execution System)




- Special Build Documentation and Line Support

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.

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.

📌 JTP 571 ENGINEERING SPECIALIST (Villalba)
🏢 Azienda importante del settore
📍 Villalba