Veeva QDocs Consultant____ Remote Contract
Job Title: Veeva QDocs Consultant
Location: Remote (EST Hours - USA)
Long Term Contract
Job Summary:
We are seeking a skilled Veeva QualityDocs (QDocs) Consultant to lead the implementation, configuration, and support of Veeva Vault QualityDocs within a regulated, GxP-compliant environment. The ideal candidate has experience with quality document management systems, strong knowledge of Veeva Vault, and a solid understanding of quality processes in the Life Sciences industry.
Key Responsibilities:
• Configure and optimize Veeva QualityDocs workflows, roles, and permissions
• Support implementation, validation, and system upgrades
• Collaborate with Quality, Compliance, and IT teams to align system with business needs
• Develop and maintain system documentation and training materials
• Ensure compliance with regulatory standards (e.g., 21 CFR Part 11, GAMP 5)
Qualifications:
• Overall IT Experience: 6-8+ years
• 3+ years of hands-on experience with Veeva Vault QualityDocs
• Strong understanding of GxP and quality management processes
• Experience in pharmaceutical, biotech, or medical device industries
• Excellent problem-solving and communication skills
• Veeva certification is a plus
To Apply :: Please share resume to [email protected]; [email protected]
Apply tot his job
Apply To this Job
Location: Remote (EST Hours - USA)
Long Term Contract
Job Summary:
We are seeking a skilled Veeva QualityDocs (QDocs) Consultant to lead the implementation, configuration, and support of Veeva Vault QualityDocs within a regulated, GxP-compliant environment. The ideal candidate has experience with quality document management systems, strong knowledge of Veeva Vault, and a solid understanding of quality processes in the Life Sciences industry.
Key Responsibilities:
• Configure and optimize Veeva QualityDocs workflows, roles, and permissions
• Support implementation, validation, and system upgrades
• Collaborate with Quality, Compliance, and IT teams to align system with business needs
• Develop and maintain system documentation and training materials
• Ensure compliance with regulatory standards (e.g., 21 CFR Part 11, GAMP 5)
Qualifications:
• Overall IT Experience: 6-8+ years
• 3+ years of hands-on experience with Veeva Vault QualityDocs
• Strong understanding of GxP and quality management processes
• Experience in pharmaceutical, biotech, or medical device industries
• Excellent problem-solving and communication skills
• Veeva certification is a plus
To Apply :: Please share resume to [email protected]; [email protected]
Apply tot his job
Apply To this Job