Clinical Validation Engineer

We are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and strokes.Join us as a Clinical...

Job DescriptionJob DescriptionWe are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and...

Validation Engineer ACADEMIC QUALIFICATIONS: Bachelor's degree in a Science or Engineering discipline with 5 years relevant experience in computer system validation. TECHNICAL QUALIFICATIONS/KNOWLEDGE: •Experience computer systems supporting R&D functions like Clinical, Pharmacovigilance/Drug Safety, Medical Affairs, Supply Chain, Regulatory Affairs and...

Validation EngineerACADEMIC QUALIFICATIONS:Bachelor’s degree in a Science or Engineering discipline with 5 years relevant experience in computer system validation.TECHNICAL QUALIFICATIONS/KNOWLEDGE:• Experience computer systems supporting R&D functions like Clinical, Pharmacovigilance/Drug Safety, Medical Affairs, Supply Chain, Regulatory Affairs and...

Validation EngineerACADEMIC QUALIFICATIONS:Bachelor’s degree in a Science or Engineering discipline with 5 years relevant experience in computer system validation.TECHNICAL QUALIFICATIONS/KNOWLEDGE:• Experience computer systems supporting R&D functions like Clinical, Pharmacovigilance/Drug Safety, Medical Affairs, Supply Chain, Regulatory Affairs and...

Engineer, CQVPay Rate: 50-55 per hourNorwood, MAMonday - FridayContract to startB.S. in engineering, science, or an equivalent technical field.Minimum of one (1) year of relevant experience in a GCLP/GLP or CLIA/CAP environment is desirable.The Engineer I, CQV (Commissioning, Qualification, and Validation) will be responsible for delivering commissioning,...

Engineer, CQVPay Rate: 50-55 per hourNorwood, MAMonday - FridayContract to startB.S. in engineering, science, or an equivalent technical field.Minimum of one (1) year of relevant experience in a GCLP/GLP or CLIA/CAP environment is desirable.The Engineer I, CQV (Commissioning, Qualification, and Validation) will be responsible for delivering commissioning,...

We are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and strokes. Join us as a...

Job DescriptionJob DescriptionWe are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and...

This individual assures validation activities are performed in conformance with applicable Standard Operating Procedures (SOPs) client standards industry best practices and regulatory requirements. The individual performs validation program-related activities such as DQ COM IQ OQ PQ CQ RQ etc.Essential Duties and Responsibilities• Writes and...

Responsibilities: Support CQV requirements, validation planning, protocol generation, test execution, configuration documentation, and system release. Perform validation projects in a fast paced, facility startup schedule. Manage cross-functional relationships with site stakeholders and vendors. Requirements: 5+ years of experience in a GMP pharma/biotech...

Sequoia is seeking an Associate Validation Engineer to assist with the development and execution of validation protocols for various types processes. The Validation Engineer will be responsible for driving overall quality performance and compliance throughout the organization by defining, implementing and maintaining the validation program. Responsibilities...

Responsibilities and Requirements: Primarily responsible for the support and execution of laboratory equipment qualification and associated computer system validation activities in compliance with current cGMP regulations and client's corporate principles, quality policies, standards, and core values. You will work closely with instrument vendors,...

About Us: Design Group operates from more than 45 offices in the United States and India, providing engineering, consulting and technical services for the world's leading companies in the food and beverage, life sciences, advanced technology, industrial and other market sectors. Our nearly 1,500 technical and engineering experts have direct industry...

Job DescriptionJob DescriptionDescription:·         Senior Validation resource (CSV) with experience in UAT, Library and data listings.·         EDC Validation experience required. ·         Providing support in Quality Assurance process awareness and adherence and supporting in preparation/review process related documents like...

Our client is a leading maker of Power Management ICs and Modules for mobile devices including smartphones, tablets, wearables, and IoT devices. The company has a unique technology that helps solve power consumption in mobile devices while improving RF efficiency, as well as using a digital signal processing technique to restore linearity. They are currently...

CQV/Validation Engineer (cGMP – Pharmaceutical)Multiple Locations - USASummary:AM Technical Solutions is looking for multiple CQV resources to support major projects for various pharmaceutical clients in the US. This individual will write and execute validation protocols for new and existing, facility utilities, and process equipment.AMTS has opportunities...

Clinical Trial Manager, Start Up Job Description; (Hybrid in office 3 days peer week)At Company, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team’s expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic...

Clinical Trial Manager, Start Up Job Description; (Hybrid in office 3 days peer week)At Company, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team’s expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic...

Summary The CQV Engineer will report to the CQV Manager to execute Commissioning, Qualification and Validation activities for a client in the Boston, MA area. The ideal candidate will be responsible for executing CQV activities at the new facility and to collaborate with Global Engineering, Facilities Operations, GIS, QA and PMO throughout the life cycle...