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
The Role: ModernaTX, Inc. seeks a Sr. Engineer, Commissioning, Qualification, and Validation for its Norwood, Massachusetts location. Here’s What You’ll Do: Manage the commissioning, qualification, and validation activities for the company’s Good Manufacturing Practices (GMP) manufacturing facility. Ensure the validated
At Cumming Group, you will work on some of the worlds most exciting projects in a dynamic environment where your success is measured by the impact you make. We are one of the fastest-growing project and
Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer
Commissioning / Qualification / Validation Specialist At Salas O’Brien we tell our clients that we’re engineered for impact. This passion for making a difference applies just as much to our team as it does to our projects. That’s
CQV Engineer (Commissioning, Qualification & Validation) Location: Indianapolis, IN Travel: Up to 40% domestic & international travel Bring Critical Manufacturing Systems to Life We bring advanced manufacturing to life by delivering world‑class automation, validation, and instrumentation solutions. Our teams
Compliance Technology Group, Inc., is currently seeking Commissioning/Validation Specialists/Engineers to work on an innovated GMP construction project focused on pharmaceutical processes. Qualified candidates will participate in startup, commissioning, and validation activities for our clients within FDA regulated industries
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 and executing end-to-end
A global pharmaceutical company is seeking a Validation Engineer II based in Billerica, MA. This role involves executing validation and qualification activities for manufacturing systems, ensuring compliance with cGMP requirements. The ideal candidate will have over 4 years of
Qualification And Validation Lead Make your mark for patients UCB is embarking on one of the most significant investments in its history through the development of a new state-of-the-art biologics manufacturing campus in Georgia, USA. Designed to power
Responsable Validation Et Qualification H/F Au sein de notre service Qualit, nous recherchons un(e) Responsable Validation et Qualification pour piloter et garantir la conformit de nos activits de validation et de qualification. Vous prendrez en charge les missions suivantes : Dfinir et
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 compliance with
Location: Indianapolis, IN Travel: Up to 40% Domestic and International TravelBring Critical Manufacturing Systems to Life PACIV stands for Process Automation, Controls, Instrumentation & Validation. At PACIV, we help bring the future of advanced manufacturing to life
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 and executing end-to-end
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 computerized systems,
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes
About the Department You will be joining Fill & Finish Expansions (FFEx), which is responsible for all major expansion activities within aseptic production, solid dosage forms, finished products, fill & finish warehousing and QC across all
Job Req ID: 29337 About Supermicro: Supermicro® is a Top Tier provider of advanced server, storage, and networking solutions for Data Center, Cloud Computing, Enterprise IT, Hadoop/ Big Data, Hyperscale, HPC and IoT/Embedded customers worldwide. We
Eliyan is building NuLink, a proprietary die-to-die chiplet interconnect fabric purpose-built for AI infrastructure at hyperscale. We are seeking a highly skilled engineer to execute high speed silicon validation efforts, ensuring our silicon platforms deliver industry-leading performance,
At Sonatus, we’re driving the transformation to AI-enabled software-defined vehicles. Traditional automotive software methods can’t keep pace with consumer expectations shaped by the mobile industry—where features evolve rapidly, update seamlessly, and improve continuously. That’s why leading