At a Glance
- Tasks: Implement and configure Quality Management Systems for pharmaceutical and life sciences clients.
- Company: Leading global GxP compliance and life sciences consulting business.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Fast-paced consulting environment with strong client relationships and project diversity.
- Why this job: Make a real impact in the life sciences industry while working with innovative digital solutions.
- Qualifications: Experience in pharma, biotech, or medical devices; knowledge of QMS platforms required.
The predicted salary is between 50000 - 70000 £ per year.
Are you an experienced Quality professional with hands-on experience implementing QMS platforms?
Do you have a background in the Pharmaceutical, Biotech or Medical Devices industry and enjoy working directly with clients to deliver digital quality solutions?
If so, this could be the role for you!
We are partnered with a leading global Gx P compliance and life sciences consulting business, who are looking to hire x2 QMS Implementation Consultants to join their growing team in Barcelona.
This is a hybrid role, requiring a minimum of three days per week in the office.
Working across a range of pharmaceutical and life sciences clients, you'll support the implementation and configuration of enterprise Quality Management Systems, helping organisations improve compliance and optimise their quality processes.
Key Responsibilities
- Configure and implement enterprise Quality Management Systems, including platforms such as Track Wise Digital and Veeva Vault Quality.
- Work directly with clients to understand quality processes including CAPAs, deviations, change control and document management.
- Support projects throughout the full implementation lifecycle, from requirements gathering and system configuration through to testing, training, go-live and post-implementation support.
- Build strong relationships with clients, providing expert guidance throughout project delivery.
- Work across multiple client projects in a fast‑paced consulting environment.
- Collaborate with internal project teams to deliver high-quality solutions that meet regulatory and business requirements.
Qualifications
- Previous experience within the pharmaceutical, biotechnology or medical device industry.
- Strong understanding of GMP, Gx P, CAPAs, deviations, change control and quality management processes.
- Hands‑on experience with enterprise QMS platforms such as Track Wise, Veeva Vault Quality or similar.
- Experience with Veeva CRM or Salesforce within a life sciences environment would be advantageous.
- Excellent client‑facing communication and stakeholder management skills.
- Professional level English and a minimum of B1 level Spanish.
- Based in Barcelona or willing to relocate for a hybrid working arrangement.
- #J-18808-Ljbffr
Contact Details:
Advanced Resource Managers Ltd Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land QMS Implementation Consultant in Barcelona
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We think you need these skills to ace QMS Implementation Consultant in Barcelona
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