Empleos de MG STAFFING GROUP en Puerto Rico

Responsibilities: · Assess the impact of IT reports, applications, software, and hardware changes on manufacturing processes and equipment. · Plan, execute, and document Computer Systems Validation (CSV) activities, including validation protocols, execution, and final reports. · ...

The Quality Application Specialist supports product transfer activities with a primary focus on process validation, sterilization processes, and commercial release readiness. This role ensures compliant execution of validation activities and quality system requirements in alignme ...

We are seeking a Validation Engineer to support a short-term onsite project within a regulated medical device manufacturing environment. · Bachelor's degree in Engineering Mechanical Electrical or Chemical preferred · years of experience in validation life cycle process Equipment ...

The Quality Application Specialist supports product transfer activities with a primary focus on process validation, sterilization processes, and commercial release readiness. This role ensures compliant execution of validation activities and quality system requirements in alignme ...

Manufacturing Engineer will support the introduction of new products and manufacturing processes within a regulated medical device environment. The role focuses on equipment validation, process development, and ensuring manufacturing processes comply with regulatory and quality r ...

Identify molecular targets that play a key role in specific disease processes. Study living organisms including bacteria and other microorganisms. · Conduct research on biological properties of substances. Isolate purify analyze identify hormones minerals proteins microbial cultu ...

Summary · The Quality Applications Specialist supports quality systems and product transfer activities by ensuring compliant validation of computerized systems and manufacturing processes. The role focuses on sterilization equipment, process validation, and quality system complia ...

Design manufacturing processes, procedures, and production layouts for assemblies, equipment installation, machining, processing, and material handling. · Design and optimize equipment and machine arrangements within plant facilities to improve productivity and workflow efficienc ...

The Sr. IT Technologist delivers advanced hands-on infrastructure support across office manufacturing distribution administrative laboratory environments ensuring infrastructure stability uptime operational excellence while collaborating with local global IT teams. · ...

The Packaging Engineer will be responsible for designing, developing, validating, and optimizing packaging systems to support Product Transfer and New Product Introduction (NPI) initiatives. This role requires hands-on experience working with packaging lines, filling equipment, a ...

Lead and execute Computer System Validation (CSV) activities for Quality Information Technology systems in compliance with FDA, GxP, ISO, and global regulatory requirements. · Conduct and maintain formal validation documentation, including Validation Plans, Risk Assessments, IQ, ...