Position Overview Position Description We are hiring a Validations Engineer. The Validations Engineer will be perform validation activities related to processes, equipment, test methods, computerized systems, and facilities. Company Overview At FUJIFILM Biosciences, we turn curiosity into breakthroughs that advance the
The Senior Software Verification and Validation Engineer is responsible for planning, developing, executing, and documenting software verification and validation activities for embedded software used in ASP capital systems. This role supports manual and automated testing, requirements-based verification, defect investigation,
Step into the innovative world of LG Electronics. As a global leader in technology, LG Electronics is dedicated to creating innovative solutions for a better life. Our brand promise, Lifes Good, embodies our commitment to ensuring
The Senior Software Verification and Validation Engineer is responsible for planning, developing, executing, and documenting software verification and validation activities for embedded software used in ASP capital systems. This role supports manual and automated testing, requirements-based verification, defect investigation,
Date Posted:2026-07-13 Country:United States of America Location:US-MA-ANDOVER-AN3 ~ 354 Lowell St ~ AN3 SUFFOLK BLDG Position Role Type:Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active and transferable U.S. government issued security clearance is required
Use Your Power for Purpose The Rochester Senior Validation Engineer is responsible for planning, scheduling, executing and leading various validation project assignments such as qualification, validation, and requalification activities related to manufacturing process, equipment, critical utility systems, product, cleaning, and/or
SOKOL GxP Services is seeking a mid-level Validation Engineer to support equipment qualification activities at a regulated life sciences facility in California. The Validation Engineer will be responsible for authoring and executing commissioning, qualification, and validation (CQV) lifecycle deliverables for manufacturing
JD: Minimum 8+ years of experience Experience working with - ARP4754A, Guidelines for development of civil aircraft and systems - Flight Control Computers and System Integration lab test setup environments. - Understand System Requirements and develop
Cryoport Systems is a comprehensive supply chain partner for the life sciences industry, delivering specialized solutions to meet the challenges of the biopharmaceutical, cell and gene therapy, reproductive medicine, and animal health markets. Our offerings span
Date Posted:2026-07-31 Country:United States of America Location:US-MA-ANDOVER-AN3 ~ 354 Lowell St ~ AN3 SUFFOLK BLDG Position Role Type:Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: The ability to obtain and maintain a U.S. government issued
Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, and customer-oriented culture is rooted in science and risk-based compliance. Whether
Use Your Power for Purpose The Principal Validation Engineer under Andover Site Technical Services (STS) is the principal owner of the Pfizer (PGS) Andover site validation program and master plan. The incumbent is responsible for delivering overall site validation program
SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this
Company Overview At Motorola Solutions, we believe that everything starts with our people. We’re a global close-knit community, united by the relentless pursuit to help keep people safer everywhere. We build and connect technologies to help
Description JOB SUMMARY: The Senior Engineer is responsible for the design of components and assemblies for medical devices as part of the new product development team and will be involved with all phases of the product development
Company Description Sandisk understands how people and businesses consume data and we relentlessly innovate to deliver solutions that enable today’s needs and tomorrow’s next big ideas. With a rich history of groundbreaking innovations in Flash and
Overview The Manufacturing Engineer 2 plans, directs, and coordinates manufacturing processes for medical device products, and supports Operations in a way to assure a quality product is produced in a timely manner. The Manufacturing Engineer works with Operations,
Overview The Supplier Quality Engineer (SQE) is responsible for the qualification, approval, and ongoing monitoring of suppliers to ensure compliance with Cook Polymer Technology quality standards and regulatory requirements. Core responsibilities include the planning and execution of
Our F500 Medical Device client has an exciting opportunity for an Electrical Engineer. Responsibilities and Job Requirements: •Identifying gaps in the acquired company’s compliance to Client’s Work Instructions and SOPs and defining strategy to close these gaps.
Company Description We are committed to our culture that values Customer Focus, Flexibility, Knowledge, Speed and Integrity. Joining our team means you will work in a high performing global company where employees collaborate and strive for