Veeva QMS

RxCloud Services India PVT LTD; Foster City (CA); On-site; USD 120,000 - 160,000; Part time

Job summary

RxCloud Services India PVT LTD in Foster City, CA is seeking a Veeva QMS Admin to lead QMS configurations and deployments. The role requires hands-on experience with Veeva Vault QMS, Q Docs, and Compliance Wire, plus familiarity with GMP workflows.

You will collaborate with clients and internal teams, provide end-user training, and develop project documentation. A Bachelor’s degree in CS/IT and 7+ years implementing Veeva QMS are required; PST hours are expected.

Qualifications

• Bachelor's degree in Computer Science, Information Technology or related field.
• 7+ years implementing Veeva QMS solutions in pharma.
• Strong knowledge of quality management processes in the pharmaceutical and life sciences industry.

Responsibilities

• Lead the implementation of Veeva QMS solutions for clients, including configuration, testing and deployment activities.
• Collaborate with project stakeholders, including clients and internal teams, to define 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.

Skills

Veeva Vault QMS

QA methodology familiarity

Audit & Inspection workflows

Pharma industry experience

Education

Bachelor's degree in Computer Science/IT or related field

Tools

Veeva Vault Q Docs/QMS configuration

Compliance Wire configuration

Job description

Role:: Veeva QMS Admin
Duration :: Long Term
Term :: W2/C2c/1099
Location:: Foster City, CA - Onsite.

Job Description

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.

Trackwise:

• Must be willing to work PST hours
• Must have experience in the Pharmaceutical industry
• Must have 8+ years of relevant experience
• Veeva Vault Quality Docs
• Experience in Veeva Vault Q Docs/QMS configuration - Must
• Experience in Compliance Wire configuration - Must
• Systems IQ/OQ/PQ in the Pharma industry

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 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.