Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON)
Computer Systems Validation (CSV) Specialist Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families. The Computer Systems Validation (CSV) Specialist helps to lead team members to assess new and changing computer systems to ensure compliance with company
At Corbion, we exist to champion preservation in all its forms, preserving food and food production, health, and our planet. The CSV IT Engineer is responsible for ensuring that computerized systems used in Corbion-regulated environments comply with applicable
Computer Systems Validation Engineer Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. The Computer Systems Validation (CSV) Engineer will, as an individual contributor, identify and implement industry best practices through an extensive industry
Validation Engineer - CSV / Computer Systems Job Opportunity Location: Fully Onsite in Lititz, PA Hiring Method: 12 Month Contract with Potential for extensions 10 Days of PTO / 6 Sick Days / Company Holidays Shift: 1st Shift
W2 Contract Onsite in Rahway, NJ JD: o Experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. o Experience of CSV Validation in any one of the Lab systems is must.
Quality Management Specialist Understand and adhere to the Client Regulations/Processes, SOP on Project Management, Change Management, Document Management and Quality Management; and, Computerized System Validation concept with regards to document management, and V Model Methodology. Support the Project Manager
Senior Manager, GxP Electronic System Validation QA Redwood City, California, United States Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) inhibitors designed to
Job Title Roles and Responsibilities: Experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. Experience of CSV Validation in any one of the Lab systems is must. Should worked in pharmaceutical
Computer System Validation Specialist Computer System Validation, CSV, GxP, 21 CFR part 11, Risk Based Approach Roles and Responsibilities 10+ yrs. of experience in Computer System Validation Senior Level individual with GxP experience Ability to lead, fully knowledgeable of Agile based System development
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
In this role, you will work both collaboratively within cross-functional teams — including colleagues, consultants, vendors, and MSPs — and independently to support day-to-day operations and project-based initiatives. The primary focus of the role is managing
Nature and Scope The Business Systems Analyst II (BSA-II) serves as a liaison between business stakeholders and information technology, translating business needs into system requirements and ensuring technology solutions support operational, regulatory, and quality objectives. This role supports
The Senior Quality Validation Specialist provides Quality Assurance oversight of validation activities across the site, with a focus on new equipment commissioning and qualification, equipment change controls, and equipment life cycle documentation. This role is responsible for ensuring
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The successful candidate will support laboratory instrument qualifications, and continuous
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Job DetailsJob Location: Scientific Protein Laboratories - Waunakee, WI 53597Job Summary Join our team at Scientific Protein Laboratories (SPL), a world leader in biosourced pharmaceuticals, located just outside of Madison, Wisconsin in Waunakee! SPL is an
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine
Position Overview The CQV Engineer 3 supports the commissioning and qualification of equipment and systems for the site. This role performs validation activities to include but not limited to equipment set up, building dashboards, creating work orders, managing