CSV Specialist - Bridgewater, NJ

As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. · Provi ...

Legend Biotech is seeking a Sr QA Validation Specialist CSV Equipment as part of the Quality team based in Raritan NJ The successful candidate will provide quality oversight over validation qualification activities for equipment systems computer systems and processes within a cel ...

++At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, · You'll be part of a community that prioritizes the human experience, ...

Legend Biotech is seeking a Sr. QA Validation Specialist based in Raritan, · NJ. · ...

Legend Biotech is seeking a Sr. QA Validation Specialist, CSV & Equipment as part of the Quality team based in Raritan NJ. · ...

Legend Biotech is seeking a Specialist, QA Process Excellence as part of the Quality team based in Raritan NJ. · Provide Quality Oversight and technical expertise to the Technical Operations and Manufacturing Teams in support of technical activities. · Provides guidance on indust ...

Legend Biotech is seeking a Specialist, QA Process Excellence as part of the Quality team based in Raritan, NJ. · ...

Legend Biotech is seeking a Specialist, QA Process Excellence as part of the Quality team based in Raritan, NJ. · ...

Legend Biotech is seeking a Specialist, QA Process Excellence as part of the Quality team based in Raritan, NJ. The role will provide quality oversight for the manufacturing process and associated technical activities within a cell therapy manufacturing plant to support both clin ...

The Legend Biotech is seeking a Specialist QA Process Excellence as part of the Quality team based in Raritan NJ . · A minimum of a Bachelor's Degree in Science or equivalent technical discipline is required. · ...

The Associate Director plays a critical leadership role overseeing team members to ensure all activities align with Regenerons procedures and industry best practices.This position collaborates closely with Clinical Data Management teams and External Data Vendors to deliver struct ...

Shape and implement the strategy for External Data Services Lead and manage a team of External Data Services Managers and Specialists Oversee the development and maintenance of all DTS documents ensuring alignment with Regeneron standards processes and timelines Drive the Externa ...

The Associate Director plays a critical leadership role overseeing team members to ensure all activities align with Regeneron's procedures and industry best practices. · ...

The Computer Validation Specialist will ensure computerized systems are in full compliance with regulatory requirements company policies and procedures.The role will contribute to the development execution review of validation deliverables for computer systems hardware software t ...

The Senior Manager - IT will serve as the strategic and operational leader of the site's technology ecosystem ensuring seamless integration of infrastructure end-user services application support and regulatory compliance. · ...

The Validation Specialist role will guide project teams through the validation process, perform regulatory risk assessments and author review and approve validation documentation.This role requires strong testing experience with broader knowledge of CSV may be considered. · Good ...

The Computer System Validation Specialist will guide project teams through the validation process and perform regulatory risk assessments. · Good communication skills · Strong knowledge on Cell therapy · 3-5 years of CSV lead experience · ...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for the Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. · The Specialist will partner with site Business Owners, CI Owners, Quality, a ...

We are one of the fastest growing IT Consulting company across the USA and we are Validation Specialist. The role will guide project teams through validation process, perform regulatory risk assessments, author review and approve validation documentation change requests and testi ...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing.This role is primarily an individual contributor but will routinely support pro ...