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Job Description
Structured overview of role & requirementsAbout This Role
Own the implementation, rollout, maintenance, and continuous improvement of Veeva QMS capabilities within VISION platform.
Translate business requirements from Quality Management, Manufacturing, Laboratory, Regulatory, and GxP stakeholders into clear functional and technical backlog items.
Manage end-to-end activities including requirements engineering, solution design, backlog management, testing, validation, deployment, and hypercare for regulated quality systems.
Minimum Requirements
Bachelor's degree in Business Informatics, Computer Science, Engineering, Quality Management, Life Sciences, Business Administration, or equivalent.
More than 10 years of relevant experience in SAP QM, LIMS, QMS systems, quality process digitalization, or regulated system implementation in healthcare, pharmaceutical, medical device, or other GxP environments.
Strong functional and technical knowledge of Quality Management processes and enterprise platforms such as Veeva QMS, SAP QM, LIMS.
Experience with product ownership or senior business roles in global QMS, ERP, or laboratory system implementation programs.
Ideal Candidate Profile
Experienced professional with deep expertise in regulated environments and computerized system validation standards like ISO 13485 and MDSAP.
Ability to bridge business process needs and technical solutions, communicating effectively with both business and IT stakeholders.
Proven capability in managing complex, international projects involving multiple stakeholders in quality and regulatory domains.