Many of the tasks will be centered around data/decisions necessary to configure the QMS workflows therefore a general knowledge of Veeva Vault is needed. Formal experience (and/o certification) in PM methodology is required. Familiarity with Audit, Inspection, Supplier Quality, and Quality Event workflows is also desirable.
Responsibilities:
Lead the implementation of Veeva QMS solutions for our clients, including configuration, testing, and deployment activities.
Collaborate with project stakeholders, including clients and internal teams, to define project requirements and ensure successful project delivery.
Provide training and support to end-users of the Veeva QMS system.
Develop and maintain project documentation, including project plans, status reports, and user manuals.
Troubleshoot and resolve technical issues related to the Veeva QMS system
Requirements:
Bachelor's degree in Computer Science, Information Technology, or a related field.
Minimum of 7 years of experience implementing Veeva QMS solutions.
Strong knowledge of quality management processes in the pharmaceutical and life sciences industry.
RxCloud is a professional services organization focused exclusively on Pharma, Biotech and Medical device industries. We are a full-scale Quality Assurance Organization driving innovation & ensuring compliance across the industry. Our mission is to deliver Quality, Compliance, Innovation, Customer Experience, and speed that enables global Life Science industry to continuously innovate and significantly reduce drug development life cycle.
We are specialized in providing the CSV services, GxP Audits (GMP, GDP, GLP, GCP, GVP) as a service, Veeva Services, Software Quality Assurance services. Our full spectrum of service offerings includes QMS Consulting, End to End Global Audit Management, CAPA management, SOP Authoring, QA as a service. RxCloud’s differentiation is bringing in speed and agility to achieve compliance first time and every time.
