Lead Validation Specialist - Princeton
3 weeks ago
Job summary
We are seeking an experienced Lead Validation Specialist with experience in clinical systems to join our team.
Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
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 ...
2 weeks ago
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 ...
2 weeks ago
We are one of the fastest growing IT Consulting company across the USA and we are hiring Validation Specialist for one of our clients. · Responsibilities i Apply FDA, MHRA, and other applicable global health authority regulations to the development of computer systems supporting ...
2 weeks ago
Apply FDA, MHRA, · and other applicable global health authority regulations to · the development of computer systems supporting regulated business processes. · ...
2 weeks ago
6+ years' experience in computer system validation. · Apply FDA, MHRA, and other applicable global health authority regulations to the development of computer systems. · FOLLOW SOPs AND industry best practices. · ...
2 weeks ago
The job requires experience in the industry and knowledge of computer systems supporting regulated business processes. · ...
2 weeks ago
A Validation Specialist with 5+ years of experience in applying FDA, MHRA, and other global health authority regulations to computer systems supporting regulated business processes. · ...
2 weeks ago
We are seeking an experienced Lead Validation Specialist with experience in clinical systems to join our team. · This is an ideal opportunity for someone who thrives in fast-paced, dynamic environments where adaptability, critical thinking and initiative are essential.About the R ...
3 weeks ago
Facilitate Computer system Validation Risk Assessment to identify governing regulations and validation deliverables during development. · Maintain close communication with stakeholders and team members. · ...
2 weeks ago
This role involves working within deadlines to read and understand Standard Operating Procedures relevant to duties. · ...
2 weeks ago
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 · ...
2 weeks ago
We are hiring QC Validation Specialist for one of our clients. Provides support of packaging validation, Quality Assurance oversight and Product Release functionality for drug products manufactured by the Contract Manufacturer. · Support packaging tech transfer · Provide reviews ...
2 weeks ago
The person will perform validation activities associated with equipment processes facilities and computer systems to ensure compliance with applicable current Good Manufacturing Practice GMP regulations site Standard Operating Procedures SOP and corporate policies. · Schedules co ...
1 month ago
Legend Biotech is seeking a Sr. Validation Specialist as part of the Quality team based in Raritan, NJ. · ...
1 month ago
We are one of the fastest growing IT Consulting company across the USA and we are hiring Validation/Compliance Specialist for one of our clients. · ...
2 weeks ago
Legend Biotech is seeking a Sr. Validation Specialist as part of the Quality team based in Raritan, NJ. · ...
1 month ago
Legend Biotech is seeking a Sr. Validation Specialist as part of the Quality team based in Raritan, NJ. · ...
1 month ago
Job summary · The Senior QA Validation Specialist role is an exempt level position with responsibilities for providing quality oversight over the validation and qualification activities for equipment systems computer systems and processes within a cell therapy manufacturing plant ...
1 month ago
This role will provide quality/compliance oversight to all computer system validation related activities across the GPS enterprise. · The manager will guide the staff to ensure a comprehensive System Development Lifecycle Methodology in alignment with GAMP 5 requirements. · ...
2 weeks ago
Legend Biotech is seeking a Sr. Validation Specialist as part of the Quality team based in Raritan, NJ. · Provide quality and compliance oversight for computer systems validation · Review and approve qualification/validation documentation (specifications, protocols) · ...
4 weeks ago