Emploi CDI Juncos

Title: Specialist QA (Job ID: ) Location: East Region, Puerto Rico (Open to Puerto Rico Residents who are U.S. Citizens) Work Model: 100% Onsite – Non-Standard Shift Contract Type: This position is offered through ProQualityNetwork as... - Voir cette offre d'emploi

*Job Overview* We are seeking a detail-oriented and knowledgeable Quality Assurance Specialist to join our team. This role is essential in ensuring that our products meet the highest standards of quality and compliance with industry regula... - Voir cette offre d'emploi

SUMMARY Perform one or more of the following duties and responsibilities in support Quality Assurance program under minimal supervision. EDUCATION/LICENSES - Doctorate degree or Master's degree and 3 years of directly related experience... - Voir cette offre d'emploi

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate worl... - Voir cette offre d'emploi

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer... - Voir cette offre d'emploi

For Quality Services in the Incoming and Warehouse area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with four (4) years of experience as a Scientist within the pharmaceutical or regulated industry. Bilingual (English... - Voir cette offre d'emploi

Title: Specialist, Manufacturing ) Location: East Region, Puerto Rico (Open to Puerto Rico residents who are U.S. citizens) Work Model: 100% Onsite – Non-Standard Shift (8-hour shift; overtime based on business needs) Contract Type: T... - Voir cette offre d'emploi

*EDUCATION: * - Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience OR Bachelor's degree and 5 years of Manufacturing Operations experience OR Associate's degree and 10 years of Manufacturing Operation... - Voir cette offre d'emploi

SUMMARY Perform one or more of the following duties and responsibilities in support of program under minimal supervision. FUNCTIONS - Review and approve product MPs. - Approve process validation protocols and reports for manufacturing ... - Voir cette offre d'emploi

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 enthusias... - Voir cette offre d'emploi