Posted on: 11/08/2025
SKILLS REQUIRED : eQMS , VeevaVault , QMS, RIM , Process Documentation, Quality Docs
ABOUT YOUR ROLE :
As a key member of the Global IT team, this role will be responsible for leading the end-to-end implementation, harmonization, and support of Veera Vault, a centralized electronic Quality Management System (eQMS) across Bio-Rads global operations. The role is pivotal in transforming the Quality Management landscape through technology, ensuring compliance, scalability, and operational efficiency.
You will work closely with cross-functional teamsincluding Regulatory Affairs (RA), Quality Assurance (QA), and external implementation partnersto drive best-in-class digital solutions that support Bio-Rads commitment to product quality, customer satisfaction, and regulatory compliance.
YOUR RESPONSIBILITIES WILL INCLUDE :
- Working closely with the leadership team and key stakeholders in the RA/QA.
- Leading the implementation and support of Veera Vault as technology platform, enabling transformation of QMS.
- Develop and execute a comprehensive implementation roadmap, including timelines, milestones, risk mitigation strategies, and change management plans.
- Partner with external Veera Vault consultants/implementation partners to ensure best-practice deployment and alignment with Bio-Rads enterprise architecture.
- Modernize and harmonize the applications to reduce the risks.
- Enhancing proactive issue detection and standardizing reporting enabling the quality culture.
- Ensuring Veera Vault technology supports best business practices and processes.
- Collaborating with cross-functional teams to develop and deliver best technology solutions.
- Act as a liaison between technical teams and business stakeholders to translate complex technical requirements into understandable business language.
- Lead steering committee updates, executive reporting, and project status reviews.
- 10 to 12+ years in IT with at least 5 years in QMS/eQMS systems implementation and 3+ years of hands-on experience with Veera Vault.
- Experience working within Life Sciences, Medical Devices, Pharmaceuticals, or other regulated industries (highly preferred).
- Strong experience in process mapping, validation documentation (IQ/OQ/PQ), and user training materials.
- Strong communication, problem-solving, and interpersonal skills. Ability to work independently and influence without authority.
WHAT WE WILL BE LOOKING FOR IN YOU :
- Degree in Computer Science or related field must have.
- Masters or higher degree in the related field preferable.
- Excellent technical and practical experience in implementation and support of VeevaVault or leading QMS systems - must have.
- Minimum 10-12 years of relevant experience must have.
- Process Documentation experience must have.
- Relevant Life Sciences industry experience highly desired.
- Proven ability to establish critical relationships, and build trust and credibility throughout the organization.
- Ability to think cross-functionally and to make sound business decisions.
- Willingness to work independently.
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Posted in
Platform Engineering / SAP/Oracle
Functional Area
Data Analysis / Business Analysis
Job Code
1528094
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