Enhanced Compliance Inc. in Santa Clarita, CA seeks a Senior Software DQA Engineer to lead software quality and validation for medical device projects, covering requirements, design, development, integration, testing and implementation. You will mentor teammates, guide validation strategies for
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Support the execution of commissioning, qualification, and validation activities for manufacturing equipment, facilities,
Cis-International-LLC in Vega Baja, Puerto Rico, seeks a highly skilled Commissioning and Qualification (C&Q) professional on a full-time, on-site basis to support a pharmaceutical manufacturing operation. The role leads qualification activities for facilities, utilities, equipment and
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Support the execution of commissioning, qualification, and validation activities for manufacturing equipment, facilities,
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Provide technical leadership for commissioning, qualification, and computer system validation activities, including: Leading
Enhanced Compliance Inc. in Santa Clarita, CA, seeks a Senior Software DQA Engineer - Medical Device to lead software quality activities across the full lifecycle, including requirements, design, development, integration, testing and validation in both Waterfall and Agile
Cis-International-LLC seeks a senior professional to provide commissioning, qualification, and computer system validation services for capital projects within a pharmaceutical manufacturing setting in Vega Baja, Puerto Rico. The role leads end-to-end qualification, develops validation lifecycle documentation, and ensures
Conde InduServices Corp. is contracted to support commissioning, qualification, and validation activities for pharmaceutical capital projects in Puerto Rico. The team will execute IQ/OQ/PQ protocols, collect data, and prepare final validation reports. We seek engineers or scientists with up
Who We Are Sunco is one of the largest and fastest-growing online lighting retailers in the U.S.—and we’re just getting started. Headquartered in sunny Valencia, CA, we’re powered by an amazing team of people who bring
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Provide technical leadership for commissioning, qualification, and computer system validation activities, including: Leading
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Support the execution of commissioning, qualification, and validation activities for manufacturing equipment, facilities,
Conde InduServices Corp. in Vega Baja, Puerto Rico is seeking an experienced professional to lead commissioning, qualification, and computer system validation efforts for capital projects in a pharmaceutical manufacturing setting. The role is a full-time, on-site engagement
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Provide technical leadership for commissioning, qualification, and computer system validation activities, including: Leading
Summary Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico. Responsibilities Provide technical leadership for commissioning, qualification, and computer system validation activities, including: Leading
Sonova Group in Valencia, CA, is seeking a Senior Engineer for Operations Quality. This role is pivotal in ensuring compliance with manufacturing controls for medical devices. Youll partner with cross-functional teams to maintain streamlined production processes and
A medical technology company in Santa Clarita is seeking a Software Validation Quality Engineer to join their Quality Assurance team. This role involves ensuring software systems meet compliance standards, executing validation protocols, and supporting process improvements within a collaborative
Base pay range $110,000.00/yr - $140,000.00/yr At HuMannity Medtec, we pioneer life-enhancing medical technologies for under met healthcare needs. Come join our team of engineers, scientists and medical device experts who are inspired to develop innovative solutions
RELOCATION ASSISTANCE: Relocation assistance may be available CLEARANCE REQUIRED FOR START: No CLEARANCE TYPE: Secret TRAVEL: Yes, 10% of the Time DescriptionAt Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact
Ford Energy is a newly formed, wholly-owned subsidiary of Ford Motor Company dedicated to accelerating U.S. energy independence. Leveraging Ford’s century of manufacturing excellence and world-class battery energy storage systems (BESS) technology, Ford Energy designs, manufactures,
UTA seeks a Senior Product Security Engineer to help embed security into the design, development, and operation of our products and platforms. In this role, you will work closely with engineering, product, and security teams to design