Job Title: Validation - Veeva QualityDocs Engineer
Work Mode: Remote
Job Type: Full-Time
Job Summary:
We are seeking a skilled and experienced Veeva QualityDocs Engineer to join our Life Sciences technology team. The ideal candidate will have deep expertise in Veeva Vault QualityDocs, with hands-on experience in configuration, customization, and integration of Veeva Vault applications within regulated environments. You will work closely with QA, IT, and business stakeholders to ensure seamless document management and compliance with GxP standards.
Key Responsibilities:
- Configure and maintain Veeva Vault QualityDocs applications to meet business and regulatory requirements.
- Collaborate with cross-functional teams to gather requirements and translate them into technical solutions.
- Develop and maintain workflows, document lifecycles, and user roles within Veeva Vault.
- Support validation activities including authoring and executing test scripts (IQ/OQ/PQ).
- Troubleshoot and resolve issues related to Veeva Vault QualityDocs.
- Ensure compliance with GxP, FDA 21 CFR Part 11, and other regulatory standards.
- Provide training and support to end-users and stakeholders.
- Participate in system upgrades, patches, and release management.
- Document system configurations, SOPs, and technical specifications.
Required Skills & Qualifications:
- 68 years of experience in IT with at least 35 years in Veeva Vault QualityDocs.
- Strong understanding of document management systems in the pharmaceutical or life sciences domain.
- Experience with Veeva Vault configuration, workflows, and lifecycle management.
- Familiarity with GxP compliance and validation documentation.
- Excellent problem-solving and communication skills.
- Ability to work independently and in a team-oriented environment.
- Veeva Vault certification is a plus.
- Experience with Agile/Scrum methodologies is desirable.
Education:
- Bachelor's or Master's degree in Computer Science, Information Technology, Life Sciences, or related field.
