MG STAFFING GROUP Jobs in United States

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 ...

The Quality Engineer II supports manufacturing and validation activities within a regulated medical device environment. · Perform and/or review Process Validation (PV) activities including characterization, OQ, and PQ (excluding cleaning validations). · ...

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 ...

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 ...

The Engineering Program Manager – Manufacturing Execution System (MES) will lead the planning, governance, and execution of MES initiatives supporting manufacturing operations at the Ponce manufacturing site. The role is responsible for ensuring successful implementation and sust ...

Assess the impact of IT reports on manufacturing processes and equipment. Plan, execute and document Computer Systems Validation activities. · Responsibilities: · Assess the impact of IT reports... · ...

Serve as a strategic HR partner to the Supply Chain function providing input into business and people strategy. · Represent the OneHR model and provide strategic guidance aligned to business objectives. · ...

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 ...

Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of oper ...

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 ...