QMS Implementation Consultant
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Job description
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Configure and implement quality management systems (e.g. TrackWise Digital, Veeva Vault Quality) according to each client’s specific needs - this is configuration, not coding.
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Work directly with pharma clients to understand their quality processes (CAPAs, deviations, change control, document management) and translate them into system configurations.
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Support clients through the full implementation lifecycle: requirements gathering, system setup, testing, training, go-live and post-deployment support.
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Work in a project-based consulting environment with different clients and challenges on each engagement., Linkedin or Dropbox URL This is a required field A valid LinkedIn URL is required, please ensure it begins with https://www.linkedin.com/ A valid DropBox URL is required, please ensure it begins with https://www.dropbox.com
Requirements
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Background in Quality in the pharmaceutical, biotech or medical device industry - understands GMP, GxP, CAPAs, deviations, change control and audit processes from real experience.
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Hands-on experience with enterprise QMS platforms (TrackWise, Veeva Vault Quality, or similar) - beyond end-user level. Experience with Veeva CRM or Salesforce in a pharma environment is also valued.
- Consulting mindset - client-facing, proactive, comfortable working across multiple projects.
- Based in Barcelona or willing to relocate. Hybrid model: minimum 3 days/week in office.
- Spanish B1 minimum. English professional level.
- Profiles from Veeva Systems or similar consulting firms are highly relevant
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