52 results for Validation Engineer Jobs in Massachusetts, US

Job Description: The Validation Engineer is responsible for developing DQ/IQ/OQ/PQ protocols and coordinating and performing equipment qualifications, ensuring that automated process equipment that mass produce medical device consumables and other products, are designed, developed or changed in comp...

DescriptionVerista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve so...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.Our goal is to skyrocket our clients’ success, and you can be a part of ...

We Are:At Synopsys, we drive innovations that shape the way we live and connect. Our technology is central to the Era of Pervasive Intelligence, from self-driving cars to learning machines. We lead in chip design, verification, and IP integration. Join us to transform the future through continuous t...

Design Verification and Validation (V&V) Engineer (ISO 14971)MUST HAVE: Minimum 6 years of experience designing, developing, and manufacturing plastic disposable kit products for regulated industry (medical device, class II and/or class III).Duration: 12+ months – estimated to end 4/2026 (contra...

Responsible for authoring validation test protocols, managing lab test requests, executing tests, and writing reports. Participate in product development, support design experiments, collaborate on product/process changes, and develop new test methods and equipment for product validation.

Develop and implement qualification processes for product reliability, schedule and execute qualification plans, monitor validation activities, identify reliability improvement opportunities, resolve reliability issues, and provide technical guidance. Distribute reliability performance reports and r...

Job DescriptionThe Validation Engineer is responsible for developing DQ/IQ/OQ/PQ protocols and coordinating and performing equipment qualifications, ensuring that automated process equipment that mass produce medical device consumables and other products, are designed, developed or changed in compli...

Responsible for commissioning and qualification activities of biopharmaceutical process equipment in an FDA/GMP environment, preparing validation test protocols, executing projects, mentoring junior engineers, managing continuous improvement projects, and advising on SOPs related to validation.

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAble to lift 40 lbs. without assistance, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Loud Noises (Equipment/Ma...