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
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
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
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.
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
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
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,
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
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
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
Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For mission-critical and regulated industries that need to deliver critical solutions in high-stakes
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global
Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological
We Participate in E-verify Formel D is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a
At Polaris Inc., we have fun doing what we love by driving change and innovation. We empower employees to take on challenging assignments and roles with an elevated level of responsibility in our agile working environment.