Computer System Validation Specialist

Description We're looking for a Validation Specialist I , working in Pharmaceuticals and Medical Products industry in 55 Corporate Drive, Bridgewater, New Jersey, 08807, United States . Job description: Manages system documentation review, storage, versioning and signature collection. Interacts with end users to gather business requirements and information...

If you are unable to click on links above to submit resume, you may email your resume to jobs@iit-inc.com Subject= IIT Career Site/Resume for JobID=15269 (Computer Support Specialists) in New York NY 10004 (SJU) Estimated Length: 12 months M-F, 37.5 hours per week Requirements Job Description/Duties The Business Requirements Analyst’s role is to elicit,...

Job DescriptionJob DescriptionComputer Support SpecialistsNew York, NY – Long-Term Contract100% On-SiteFusco Personnel is actively recruiting for Computer Support Specialists to join our client located in the New York, NY area. This is a full-time, long-term contract opportunity. The ideal candidate will have prior experience working within the NYS system,...

Job DescriptionJob DescriptionComputer Support SpecialistsNew York, NY – Long-Term Contract100% On-SiteFusco Personnel is actively recruiting for Computer Support Specialists to join our client located in the New York, NY area. This is a full-time, long-term contract opportunity. The ideal candidate will have prior experience working within the NYS system,...

**Product Validation Engineering Technician - System Performance 1st Shift** **Pay Range $30.46- $45.69** Our culture believes in _POWERING YOUR POTENTIAL_. We provide global opportunities to develop your career, make your community a better place and work with today’s most innovative thinkers to solve the world’s toughest problems. We believe in...

Job Description Planning, preparation, conduct, reporting and follow up of various types of audits according to expected quality and timelines Executing audits based on a comprehensive understanding of all regulatory requirements. Performing quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry. Assisting...

Job Description Planning, preparation, conduct, reporting and follow up of various types of audits according to expected quality and timelines Executing audits based on a comprehensive understanding of all regulatory requirements. Performing quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry. Assisting...

Job Description Planning, preparation, conduct, reporting and follow up of various types of audits according to expected quality and timelines Executing audits based on a comprehensive understanding of all regulatory requirements. Performing quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry. ...

Job Description Planning, preparation, conduct, reporting and follow up of various types of audits according to expected quality and timelines Executing audits based on a comprehensive understanding of all regulatory requirements. Performing quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry. ...

Job Duties:Analyze existing computer systems and engineer solutions to cloud (PCF and Azure) based enterprise-level computer application problems; perform requirement gathering and analysis; establish functional design specifications and Azure preferences by mapping conceptual business needs and requirements into practical system capabilities; prepare system...

Job Duties:Analyze existing computer systems and engineer solutions to cloud (PCF and Azure) based enterprise-level computer application problems; perform requirement gathering and analysis; establish functional design specifications and Azure preferences by mapping conceptual business needs and requirements into practical system capabilities; prepare system...

Company DescriptionTHIS ROLE CAN BE BASED ANYWHERE IN EASTERN OR MID USA or Eastern Canada ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice...

Company DescriptionTHIS ROLE CAN BE BASED ANYWHERE IN EASTERN OR MID USA or Eastern Canada ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice...

Vista Global Solutions, LLC., as part of Bristol Bay Native Corporation, is primarily focused on providing information technology (IT) support services and personnel to various government customers. We help our customers leverage technology and operate with total confidence in their technology resources predictability, security, and reliability to meet...

Job DescriptionJob DescriptionCompany DescriptionTHIS ROLE CAN BE BASED ANYWHERE IN EASTERN OR MID USA or Eastern CanadaADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP),...

Job DescriptionJob DescriptionWhy Join ADAPT?It's more than a job; it's a calling. It's where passion meets purpose. ADAPT Community Network, formerly United Cerebral Palsy (UCP) of NYC provides many services to people with developmental disabilities. At ADAPT, we are 3,000 strong, and it takes every one of us to empower the lives of the people...

Job DescriptionJob DescriptionWhy Join ADAPT?It's more than a job; it's a calling. It's where passion meets purpose. ADAPT Community Network, formerly United Cerebral Palsy (UCP) of NYC provides many services to people with developmental disabilities. At ADAPT, we are 3,000 strong, and it takes every one of us to empower the lives of the people...

Summary of Primary Responsibilities: This position is responsible for managing the Bedford Site’s Validation program that includes start-up, commissioning, qualification, validation and revalidation projects for facility, equipment, critical utility, automation/computer system, cleaning, sterilization, and medical device/drug product manufacturing...

Key Responsibilities Strong Experience in Computer Systems Validation (CSV) within the pharmaceutical industry. Required Bachelor's degree in pharmaceutical Science OR related field of study. Schedule and plan equipment and process qualification workload to meet approved schedules. Handle multiple projects and be able to work independently as required....

Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Validation Engineer to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference! Shift : M-F 1st shift Type : 7...