Veolia is seeking a Senior Process Engineer to join the Technical Direction and Process Validation team in the United States. The role involves evaluating opportunities, developing PFDs/P&IDs, and supporting Sales and Commercial Engineering with process expertise. You will lead design
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
The Process Improvement Coordinator is responsible for identifying, developing, and implementing process improvement initiatives that enhance operational efficiency, product quality, productivity, and customer satisfaction. This position analyzes manufacturing and business processes, monitors performance metrics, supports continuous improvement initiatives,
Company Description Veolia Group is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management, Veolia Group designs and implements innovative solutions for decarbonization,
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Bristol Myers Squibb in New Brunswick, NJ, is seeking a Process Development Engineer for Device and Packaging Development to advance fill-finish and device assembly processes for sterile drug products. The role requires collaboration with Clinical and Commercial
# Process Development Engineer, Device and Packaging DevelopmentNew Brunswick - NJ - USFind out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job.
Company Description Veolia Group is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management, Veolia Group designs and implements innovative solutions for decarbonization,
Veolia is seeking a Senior Process Engineer to join the Technical Direction and Process Validation team in Trevose, PA. You will collaborate with Process Engineers and SMEs to evaluate projects involving new construction, fleet-based solutions, and repurposing existing assets for
Project Manager, Validation page is loaded# Project Manager, Validationlocations: East Brunswick, NJtime type: Full timeposted on: Posted Todayjob requisition id: R020999BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Director of Compliance & Validation, Life Sciences Location: East Brunswick, New JerseyWho You’ll Work With You will join our East Brunswick, New Jersey office, be part of a committed organization of over 1,500 professionals, and work in
Who You’ll Work With You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work
Job Description Reporting to the Technical Director and serving as a member of the Technical Direction and Process Validation (TDPV) team, the Senior Process Engineer will collaborate with Process Engineers and Subject Matter Experts (SMEs) to evaluate potential projects and
Project Manager, Validation You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is
Manager, IT Validation Services Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day,
Computer System Validation Specialist 10+ years experience in computer system validation or quality management or business analysis in GxP application area Has working experience in any one or two of the following domains - clinical development and supply
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
IT Quality Compliance Specialist/Analyst Hybrid role-Local Candidates Only Work Schedule: Mon - Fri, Business HoursMust haves: Ideal candidate would have prior experience of Labelling system (Esko - Web Center, Bonitasoft BPM) Quality assurance mindset for computer