Sr. Quality Applications Specialist - Juncos, PR

Lead and execute Computer System Validation (CSV) activities for Quality Information Technology systems in compliance with FDA, GxP, ISO regulatory requirements. Conduct and maintain formal validation documentation. Provide quality leadership to peers. Perform system administrati ...

We are looking for a talented, highly motivated and enthusiastic Associate Quality Applications Specialist to join our team in Puerto Rico & USA. · ...

For validation services in the Manufacturing area. · Conducts a compliant validation process for quality information technology systems · Cordinates activities with clients programmers developers and operating personnel domestic and global · ...

We are looking for a talented Quality Applications Specialist to join our team in Puerto Rico & USA. · Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under ...

For validation services in the Manufacturing area. · Bachelor's Degree in Engineering and (4) four years of experience within the Medical Devices Industry. · ...

· 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-cla ...

· 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-cla ...

+Quality Consulting Group is looking for an Associate Quality Applications Specialist to join their team. · +Conducts a compliant validation process for quality information technology systems. · Liaise with clients and programmers to ensure system compliance. · ...

We are looking for a talented Quality Applications Specialist to join our team. · ...

We are looking for a Quality Application Specialist to conduct validation processes for quality information technology systems and coordinate activities with clients and personnel. · ...

· For validation services in the Manufacturing area. · WHAT MAKES YOU A FIT:  · The Technical Part: · Bachelor's Degree in Engineering and (4) four years of experience within the Medical Devices Industry. · Bilingual: Spanish and English · Soft Skills: Excellent Team leader skil ...

· For validation services in the Manufacturing area. · WHAT MAKES YOU A FIT:  · The Technical Part: · Bachelor's Degree in Engineering and over one year of experience within the Medical Devices Industry. · Bilingual: Spanish and English · Soft Skills: Excellent Team leader skill ...

Conducts a compliant validation process for quality information technology systems. · ...

· Assesses impact of IT reports/applications/software/hardware changes on process and equipment · Coaches and reviews work of lower-level specialists · ...

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We are looking for a talented and highly motivated manufacturing engineer to join our team in Puerto Rico & USA. · ...

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 ...

+We are looking for a talented and motivated Senior Engineer to join our team. In this role, you will work with a highly enthusiastic team in the manufacturing industry in Puerto Rico & USA. · +Provides characterization of process optimization strategies and/or troubleshooting of ...

For Validation services in the Engineering area. · WHAT MAKES YOU A FIT:  · The Technical Part: · Bachelor's Degree with four (4) years of experience as an Engineer within the pharmaceutical or regulated industry. · Bilingual (English & Spanish). · Project Management skills. · Sh ...