Validation Engineer

VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences...

VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences...

VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences...

Responsibilities: Validation Strategy: Develop validation strategies aligned with regulatory standards. Protocol Generation: Author and review validation protocols for processes and equipment. Execution: Lead validation studies and analyze data, ensuring adherence to timelines. Reporting: Prepare comprehensive validation reports with findings and...

Responsibilities: Write technical documents associated with projects. Write engineering and design specifications (URS/FS/DS) and protocols (IQ/OQ/PQ/CSV) for facility and utility systems. Perform (hands on) field execution of commissioning and/or validation documentation. Reviewing equipment lists, instrument lists, drawings, specifications, and submittals...

Responsibilities: Validation Strategy: Develop validation strategies aligned with regulatory standards. Protocol Generation: Author and review validation protocols for processes and equipment. Execution: Lead validation studies and analyze data, ensuring adherence to timelines. Reporting: Prepare comprehensive validation reports with findings and...

Teamwork makes the stream work.Roku is changing how the world watches TVRoku is the #1 TV streaming platform in the US, and we've set our sights on powering every television in the world. Roku pioneered streaming to the TV. Our mission is to be the TV streaming platform that connects the entire TV ecosystem. We connect consumers to the content they love,...

Role: Validation Engineer - Pharma Location: CA Duration: 12 Months on W2 - No C2C Please do apply if you have minimum 3+ years of experience as a Validation Engineer in Life Sciences Industry (Medical Device/Pharma/Biotechnology) We are looking for a Senior Validation Engineer to assist with a large-scale, production suite expansion project with our...

Role: Validation Engineer - PharmaLocation: CADuration: 12 Months on W2 - No C2CPlease do apply if you have minimum 3+ years of experience as a Validation Engineer in Life Sciences Industry (Medical Device/Pharma/Biotechnology)We are looking for a Senior Validation Engineer to assist with a large-scale, production suite expansion project with our...

Role: Validation Engineer - PharmaLocation: CADuration: 12 Months on W2 - No C2CPlease do apply if you have minimum 3+ years of experience as a Validation Engineer in Life Sciences Industry (Medical Device/Pharma/Biotechnology)We are looking for a Senior Validation Engineer to assist with a large-scale, production suite expansion project with our...

Role: Validation Engineer - PharmaLocation: CADuration: 12 Months on W2 - No C2CPlease do apply if you have minimum 3+ years of experience as a Validation Engineer in Life Sciences Industry (Medical Device/Pharma/Biotechnology)We are looking for a Senior Validation Engineer to assist with a large-scale, production suite expansion project with our...

San Jose, CA Full-time $160,000.00 - $240,000.00Posted 12/07/2023Job Title: Principal Validation Engineer - SerDesJob Location: San Jose, CACompensation: $160K - $240K base Depending on experience plus significant equity!Requirements: Validation, SerDes, High-Speed Interconnects, PCIe, CXL, Ethernet, Testing We were founded in 2020 by a team of veterans in...

Job Description: Pay Range $70.80 hr - $74.80hr Responsible for performing process, equipment, and software validation activities including, but not limited to, gathering historical data for product manufacture, analyzing data using statistical principles, writing validation protocols and reports, GDP review of data and reports, and final approval of...

AMS Silicon validation Engineer (Analog Mixed Signal Validation Engineer)Bay Area, CAPermanent RoleThe main function of an AMS silicon validation engineer is to perform lab characterization and validation of various analog & mixed signal circuits and collaborate with multi-functional teams to bring the world class silicon system into market.Job...

AMS Silicon validation Engineer (Analog Mixed Signal Validation Engineer)Bay Area, CAPermanent RoleThe main function of an AMS silicon validation engineer is to perform lab characterization and validation of various analog & mixed signal circuits and collaborate with multi-functional teams to bring the world class silicon system into market.Job...

Job Responsibilities: Work with a small team of product engineers in developing optical designs & validation systems for AR applications Support Audio design iterations, validations and simulations. Collaborate with cross-functional teams and suppliers in building prototypes and testing sequences. Collaborate with the larger research team to explore...

E-CQR is a San Diego based company and offers a broad range of business solutions and technology services to help clients in achieving their business goals. Our top notch consultants are providing services to industry's top Pharmaceutical Biotechnology Medical device Clinical research Diagnostics Chemical Bio Medical Drug development ...

E-CQR is a San Diego based company and offers a broad range of business solutions and technology services to help clients in achieving their business goals. Our top notch consultants are providing services to industry's top Pharmaceutical Biotechnology Medical device Clinical research Diagnostics Chemical Bio Medical Drug development Bioinformatics and...

Responsibilities: Write qualification and validation protocols/reports and other documentation related to the activities Responsible for performing process and equipment validation activities including, but not limited to, gathering historical data for product manufacture, analyzing data using statistical principles, writing validation protocols and...

RoleThe Validation Engineer will be responsible for completing the commissioning and qualification activities for the equipment and systems included in a new Sterility Suite at one of our clients. The Sterility Suite will be created as part of a facility upgrade project to reconfigure an existing space into a new Grade D clean suite. The qualification will...