Sr Associate Automation - Juncos

The Sr. Associate Mfg Systems provides technical engineering support in a highly automated manufacturing environment. This role supports system and equipment optimization strategies, upgrades, replacements, and modifications while ensuring maintenance and manufacturing systems re ...

The Sr. Associate Mfg Systems provides technical engineering support in a highly automated manufacturing environment. This role supports system and equipment optimization strategies, upgrades, replacements, and modifications while ensuring maintenance and manufacturing systems re ...

We are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and ...

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, Engineering, Project Management, Valid ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · The C&Q Lead – · Filling Operations: responsible for planning, executing, and managing all Commissioning and Qualification (C&Q) activities associat ...

We are united in our responsibility to create healthier futures. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. · ...

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 dynamic, contributing in a world-class manufactur ...

The Senior Associate, Manufacturing Systems (Automation) provides technical engineering support for system and equipment optimization, · Evaluate and ensure utility systems meet all applicable industry standards. · Maintain consistency in the maintenance team's training program a ...

We are seeking a talented individual committed to working under high ethics standards for the position of CQV Specialist. · The ideal candidate will have prior experience with biotech processes, familiarity with regulatory standards (FDA/EU Annex 15), and ability to work cross-fu ...

For mechanical and Troubleshooting services in the Engineering area. · WHAT MAKES YOU A FIT: · The Technical Part: · Bachelor's Degree or Associate Degree with six (6) years of experience in the regulated industry. · Bilingual (English & Spanish). · Problem-solving and root caus ...

Associate Tech Engineering position at QRC Group, LLC required experience with pneumatic, automatic control and vision inspection systems. · ...

CQV Specialist for Upstream Process Equipment. · The CQV Specialist for Upstream Process Equipment will be responsible for the commissioning and qualification of systems supporting cell culture operations in a cGMP biotechnology manufacturing environment. · Bachelor's degree in e ...

The Sr. Associate Mfg Systems provides technical engineering support in a highly automated manufacturing environment. This role supports system and equipment optimization strategies, upgrades, replacements, and modifications while ensuring maintenance and manufacturing systems re ...

The Sr. Associate Mfg Systems provides technical engineering support in a highly automated manufacturing environment. This role supports system and equipment optimization strategies, upgrades, replacements, and modifications while ensuring maintenance and manufacturing systems re ...

This is a great opportunity for one of our leading clients in Puerto Rico. · ...

This is a great opportunity for one of our leading clients in Puerto Rico. · Review and approve product Master Plans (MPs). · Approve process validation protocols and reports for manufacturing processes. · ...

This is a great opportunity for one of our leading clients in Puerto Rico. · Review and approve product Master Plans (MPs). · Approve process validation protocols and reports for manufacturing processes. · ...

This is a great opportunity for one of our leading clients in Puerto Rico. Under minimal supervision, support Quality Assurance program by performing a variety of key responsibilities in manufacturing, · process validation, · regulatory compliance, · & quality assurance activitie ...

+This is a great opportunity for one of our leading clients in Puerto Rico. · +Review and approve product Master Plans (MPs). · Approve process validation protocols and reports for manufacturing processes. · +Requirements · • Experience in Quality and Compliance · • Experience wi ...

Perform one or more of the following duties and responsibilities in support of Client's Quality Assurance program under minimal supervision. · ...