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
Arcus Biosciences is seeking an experienced Senior Manager, IT Qualification & Validation to join our dynamic and collaborative team. This is an opportunity to make a meaningful difference in a growing, fast-paced, clinical-stage organization. In this role, you
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
Conde InduServices Corp. seeks a technical lead for Commissioning and Qualification activities in a pharmaceutical manufacturing setting in Puerto Rico. This full-time, on-site role supports capital projects within the Engineering department as an independent contractor. Responsibilities include
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,
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
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
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
Location: Indianapolis, IN Travel: Up to 40% Domestic and International Travel Bring Critical Manufacturing Systems to Life PACIV stands for Process Automation, Controls, Instrumentation & Validation. At PACIV, we help bring the future of advanced manufacturing to
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
Arcus Biosciences seeks an experienced Senior Manager, IT Qualification & Validation to lead qualification and validation of GxP systems and IT infrastructure across the lifecycle. You will guide contract CSV resources, collaborate with IT, Quality, and business stakeholders, and ensure
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 under
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
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
Senior Manager, IT Qualification & Validation Arcus Biosciences is seeking an experienced Senior Manager, IT Qualification & Validation to join our dynamic and collaborative team. This is an opportunity to make a meaningful difference in a growing, fast-paced, clinical-stage organization.
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
Company Description The Sr Hardware Validation engineer serves as embedded hardware domain expert, driving product and platform design quality, evaluation and validation objectives, and technical execution while collaborating closely with systems, firmware/software, validation, and platform develop teams. Job Description