CPG Regulatory Expert Needed: Nutrition Facts Validation + FDA

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Join JR Automation as an FDA Validation Engineer to deliver customer success worldwide by providing intelligent automated manufacturing and distribution technology solutions. As a member of our team, you will provide validation experience and guidance during equipment design, sof ...

This is an onsite position based in Nashville, TN. · ...

Location: · Nashville, Tennessee, United States of AmericaJob ID: · R0116645Date Posted: · Company Name: · WRIGHT INDUSTRIES, LLCProfession (Job Category): · Engineering & ScienceJob Schedule:  · Full timeRemote: · NoJob Description: · JR Automation, a Hitachi Group Company, is ...

We provide intelligent automated manufacturing and distribution technology solutions that transform how the world's leading manufacturers make and distribute products. · ...

· Company Description · 360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services ...

The Regulatory Affairs Associate will lead the preparation, strategy, and submission of FDA regulatory applications for medical devices.Develop end-to-end regulatory strategies that integrate clinical evidence. · Author and contribute to clinical and scientific sections of FDA su ...

Enzo Life Sciences seeks an experienced Validation Tester to execute CFR Part 11 compliance testing supporting FDA approval processes for key pharmaceutical clients including Vertex. This hybrid position requires proven life sciences validation experience with immediate availabil ...

Our client is a large medical device manufacturer addressing FDA-driven remediation needs within manufacturing operations. They are seeking an experienced Quality Engineer to support process risk activities. · ...

Position: Senior Equipment Validation Engineer · Position Overview · We are seeking a Senior Validation Engineer to lead equipment and process validation activities in a regulated medical device manufacturing environment. This role is responsible for managing validation lifecycle ...

The Validation Engineer is responsible for planning executing and documenting validation activities for medical device manufacturing processes equipment and systems to ensure compliance with FDA ISO requirements. · ...

Software Validation Engineer (Manufacturing Equipment) – Medical Device · We are partnering with an innovative vascular medical device company in Salt Lake City that is rapidly advancing multiple FDA submissions and preparing for commercialization. As their R&D and manufacturing ...

The Client seeks an experienced Validation Tester to execute CFR Part 11 compliance testing supporting FDA approval processes for key pharmaceutical clients including Vertex. · ...

We are currently hiring multiple Validation Engineers for a pharmaceutical company that develops manufactures and markets generic pharmaceutical medicines. · Execute equipment qualification and validation activities (IQ/OQ/PQ) · Support utility and facility qualification efforts ...

The Senior IT Quality Control Specialist provides QA oversight for computerized systems validation (CSV), remediation initiatives, and software quality processes within a regulated environment. This role ensures compliance with FDA CSA principles, GxP requirements, and global reg ...

We are seeking a CQV / Validation Engineer to support commissioning, qualification, and validation activities for pharmaceutical manufacturing systems... · ...

Dice is the leading career destination for tech experts at every stage of their careers. Our client, TechVirtue LLC, is seeking the following. Apply via Dice today. · Client seeks an experienced Validation Tester to execute CFR Part 11 compliance testing supporting FDA approval p ...

Dice es el destino laboral líder para expertos en tecnología a cada etapa de sus carreras. Nuestro cliente, TechVirtue LLC, busca un Validation Tester experimentado para ejecutar pruebas de conformidad con CFR Parte 11 que apoyen procesos de aprobación FDA para clientes farmacéut ...

Seeking a Senior Equipment Validation Engineer to lead equipment and process validation activities in a regulated medical device manufacturing environment. · ...

This role oversees QA operations and partners closely with manufacturing validation and regulatory groups to ensure safe compliant high-quality drug products. · Lead and develop the Quality Assurance team including coaching training and performance management. · Oversee GMP quali ...