Veeva QMS

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 hoursMust have experience in the Pharmaceutical industryMust have 8+ years of relevant experienceVeeva 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 industryResponsibilities: 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. 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 hoursMust have experience in the Pharmaceutical industryMust have 8+ years of relevant experienceVeeva 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 industryResponsibilities: 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. 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 hoursMust have experience in the Pharmaceutical industryMust have 8+ years of relevant experienceVeeva 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 industryResponsibilities: 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.

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, 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.