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,
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
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
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
Application close date:Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We’re working to
Date Posted:2026-07-22 Country:United States of America Location:US-CA-PASADENA-4800-CUST ~ 4800 Oak Grove Dr ~ OAK GROVE (External Site) Position Role Type:Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active and transferable U.S. government issued security clearance
Company Description NBCUniversal is one of the worlds leading media and entertainment companies. We create world-class content, which we distribute across our portfolio of film, television, and streaming, and bring to life through our global theme