39 lead validation opportunities in Bridgewater updated today
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· Page 1 / 2Job Title: IM Regulatory Validation Lead Location: Raritan, NJ(Hybrid) Job Details Experienced Validation lead to support end to end validation ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack •8+ years’ experience in Computer System Validation or Quality man
Job Title: IM Regulatory Validation Lead Location: Raritan, NJ(Hybrid) Job Details: Experienced Validation lead to support end to end validation ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 8+ years’ experience in Computer System Validation or Quality man
Job Details: Experienced Validation lead to support end to end validation ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 8+ years’ experience in Computer System Validation or Quality management or Business Analysis in GxP application area Act as single poin
Job Title: IM Regulatory Validation Lead Location: Raritan, NJ (Hybrid) Job Details: Experienced Validation lead to support end to end validation ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 8+ years experience in Computer System Validation or Quality man
Job Title: IM Regulatory Validation Lead Location: Raritan, NJ(Hybrid) Job Details: Experienced Validation lead to support end to end validation ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack • 8+ years’ experience in Computer System Validation or Quality m
Senior Technical Lead Job Title: IM Regulatory Validation Lead Location: Raritan, NJ (Hybrid) W2/C2C Job Details: Technical Lead is responsible for end-to-end technical ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 1. Work with cross functional team 2. Ens
Dice is the leading career destination for tech experts at every stage of their careers. Our client, Sharpedge Solutions, is seeking the following. Apply via Dice today! **Job Title: IM Regulatory Validation Lead Location: Raritan, NJ(Hybrid) Job Details:** T echnical Lead is responsible for end-to-
Hi I hope you are doing well. We have an urgent position listed below. Please send your most recent resume along with the expected rate if you are interested. Job Role: IM Regulatory Validation Lead Location : Raritan, NJ (Hybrid) Visa: USC/GC Job Description : T echnical Lead is responsible for end
Job Details Technical Lead is responsible for end-to-end technical ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack Work with cross functional team Ensure all deliverables are met Ensure Timeline is met, Act as technical single point of contact for large regu
Cognizant is always looking for top talent. We are searching for candidates to fill future needs within the business. This job posting represents potential future employment opportunities with Cognizant. Although the position is not currently available, we want to provide you with the opportunity to
Job Title: Validation Lead with AI knowledge Location: Raritan, NJ Remote for Canada Type: Contract Role Descriptions Demonstratable Experience in Computer System Validation (CSV)Experience in software development processes (SDLC) and software testing life cycle (STLC) Experience in drafting reviewi
*Role: CSV - Validation Lead** *Location: Raritan, NJ** *Contract** *Role Descriptions:** · Demonstratable Experience in Computer System Validation (CSV)Experience in software development processes (SDLC) and software testing life cycle (STLC) · Experience in drafting| reviewing| revising| and maint
Eliassen GroupA strategic consulting company is looking for a Quality Lead to oversee the Quality Management System and ensure FDA compliance across various software initiatives. The successful candidate will guide documentation, lead validation activities, and support IT teams. A Bachelor's degree in a technical
Requirements Must have: - Proven experience in Computer System Validation (CSV) - Familiarity with software development life cycle (SDLC) and software testing life cycle (STLC) - Proficient in drafting, reviewing, revising, and maintaining validation documents including Compliance Analysis, Complian
Supporting and Validating Regulatory systems like REMS RIMS 10+ years experience in Computer System Validation of Regulatory systems like Regulatory Information Management System, REMS, Publishing, eCTD systems used in Pharmaceutical industry. Guide the project team with the right set of applicable
Sierra Business Solution LLCJob Title: Validation Lead with AI knowledge Location: Raritan, NJ Remote for Canada Type: Contract Role Descriptions: Demonstratable Experience in Computer System Validation (CSV)Experience in software development processes (SDLC) and software testing life cycle (STLC) Experience in drafting review
A strategic consulting company is looking for a Quality Lead to oversee the Quality Management System and ensure FDA compliance across various software initiatives. The successful candidate will guide documentation, lead validation activities, and support IT teams. A Bachelor's degree in a technical
An established industry player seeks a seasoned professional with over a decade of experience in Computer System Validation within the Pharmaceutical sector. This role involves supporting and validating critical regulatory systems, guiding project teams through the SDLC process, and ensuring complia
Omni InclusiveSupporting and Validating Regulatory systems like REMS RIMS 10+ years experience in Computer System Validation of Regulatory systems like Regulatory Information Management System, REMS, Publishing, eCTD systems used in Pharmaceutical industry . Guide the project team with the right set of applicable
A leading consulting firm in New Jersey is seeking an AML Model Validation and Testing Manager to lead model validation testing for Financial Crime programs. The ideal candidate will have over 4 years of experience in financial crime, strong organizational skills, and expertise in data analysis. Res
CSV for SAP systems/projects To create| assign and track the project [module] work plans for delivery and also provide technical guidance for work completion. (1.) To ensure process improvement and compliance in the assigned module| and participate in technical discussions/review. (2.) To create wor
Project Module Work Plans To create, assign, and track the project module work plans for delivery and also provide technical guidance for work completion. To ensure process improvement and compliance in the assigned module, and participate in technical discussions/review. To create work plans, monit
To create| assign and track the project [module] work plans for delivery and also provide technical guidance for work completion. (1.) To ensure process improvement and compliance in the assigned module| and participate in technical discussions/review. (2.) To create work plans| monitor and track th
Syntricate TechnologiesRequired Skills: Demonstratable Experience in Computer System Validation (CSV) Experience in software development processes (SDLC) and software testing life cycle (STLC) Experience in drafting, reviewing, revising, and maintaining validation documents (CSV), including Compliance Analysis, Compliance
A leading engineering consultancy in East Brunswick Township is seeking a Sr. Validation Engineer with over 10 years of experience in validation of pharmaceutical processes and equipment. This role involves managing validation projects, developing FDA compliance documents, and serving as the primary
A leading clinical trial organization located in South Plainfield, New Jersey is seeking a Validation Specialist. This role requires at least 8-10 years of experience in Computer System Validation, expertise in Quality Management Systems, and proficiency in software quality assurance processes. The
A contract research organization is seeking a CVS Lead responsible for leading Computer System Validation activities for GxP-regulated systems. This position involves ensuring compliance with global regulatory standards, managing validation lifecycle activities, and coordinating with cross-functiona
A leading staffing group is looking for a Test Development Engineer in New Brunswick, NJ. The role focuses on developing and validating test methods with emphasis on statistical analysis. The ideal candidate will have extensive experience in robotics or medical devices and the ability to manage and
Experience on V-Life cycle of project execution methodology Aware of FDA compliance on GAMP 5 standards Worked on Standards like ISA 95, ISA 88, B2MML, PackML etc. Handled the protocols like DeviceNet, HART, Modbus, ProfiBus, FieldBus, OPC UA, OPC DA, TIBCO, RFI, etc Certified on GAMP standards Face
$66,000 – $90,000/year
Estimation confidence: Low
Estimate based on market data for Bridgewater. Actual salaries may vary depending on experience, company, and area.
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