QMS & Implementation Consultant – Pharma

Rephine; Barcelona; Híbrido; EUR 50.000 - 70.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive compensation

Work-life balance

Opportunities for growth

Descripción de la vacante

Join Rephine in Barcelona as a QMS Implementation Consultant to lead the implementation of Quality Management Systems in the Life Sciences industry. You will work directly with clients, tailoring systems to fit their unique processes and requirements.

Your role involves not only understanding QMS platforms but also configuring processes and workflows. A background in the pharmaceutical or life sciences is essential, along with experience working with clients. Enjoy competitive compensation, a hybrid work model, and the opportunity for global exposure.

Formación

• 4–5 years of experience in Quality in pharmaceutical, biotech, or medical device industries.
• In-depth knowledge of QMS platforms and experience with systems implementation.
• Natural communicator with client-facing experience.

Responsabilidades

• Lead and support the implementation and configuration of QMS platforms.
• Translate client needs into system solutions and configurations.
• Collaborate with project teams throughout the implementation lifecycle.

Conocimientos

Quality Management Systems (QMS)

Pharmaceutical industry experience

Client communication

Problem-solving

System configuration

Herramientas

CAPA workflows

Change control

Descripción del empleo

Job Title: QMS Implementation Consultant – Life Sciences

Join Rephine Barcelona: Driving Digital Quality Systems Implementation in Life Sciences

At Rephine, we lead the way in quality assurance and GxP compliance for the Life Sciences industry. With offices in Barcelona, the UK, and China, we provide unparalleled support to global Pharmaceutical, Biotech, and Medical Device supply chains.

Who We're Looking For

Are you a quality professional from the pharma or life sciences world who knows QMS platforms inside out — not just as a daily user, but someone who has always been curious about what sits behind the screens? Do you enjoy working with clients, solving problems in different contexts, and moving from project to project? If the idea of helping organisations implement and adapt quality systems to their specific needs excites you, you might be our next QMS Implementation Consultant.

About the Role

We are looking for someone with a solid background in Quality and hands‑on knowledge of QMS platforms used in the pharmaceutical or life sciences industry. In this role, you will work on the back‑end of these systems — not as a day‑to‑day user filling in forms, but as the person who builds and adapts what those users see and interact with. You will configure workflows, set up processes such as CAPAs or audit trails, and tailor the system to match each client's specific quality needs.

This is a project‑based consulting role. Each engagement is different, each client has different needs, and your ability to listen, understand their processes, and translate them into working system configurations will be what sets you apart. No coding is involved — your expertise in quality and your understanding of how these systems work is what matters.

Key Responsibilities

• Lead and support the implementation and configuration of QMS platforms, adapting them to each client's quality processes and requirements.
• Work directly with clients to understand their needs — whether it's setting up a CAPA workflow, configuring change control, or adapting document management — and translate those needs into system solutions.
• Collaborate with project teams throughout the full implementation lifecycle: from requirements gathering and system configuration through testing, training, and go‑live.
• Troubleshoot and resolve issues proactively, always focused on practical solutions that work for the client.
• Work independently when required, ensuring tasks are completed on time and to a high standard.
• Bring your pharma quality knowledge into every project, acting as a trusted advisor to clients navigating new systems.

Who We're Looking For

• A professional with 4–5 years of experience in Quality in the pharmaceutical, biotech, or medical device industry — you understand quality processes such as CAPAs, deviations, change control, document management, and audit trails from real experience.
• Someone who has used enterprise QMS platforms and understands how they work beyond the surface — ideally someone who has been involved in a system implementation, acted as a system owner or administrator, or simply gone further than most users in understanding what the system can do.
• A natural communicator who enjoys client‑facing work and is energised by the variety of working across different projects and organisations.
• Proactive, solution‑oriented, and comfortable taking ownership of tasks independently.
• Someone who sees consulting and project‑based work as an opportunity, not a challenge — you thrive on variety and enjoy the dynamic of new clients and new problems.

Why Choose Rephine?

• Competitive Compensation: A salary that reflects your experience, along with additional vacation days and other benefits.
• Work‑Life Balance: Hybrid work model, flexible hours, and a shorter workday on Fridays.
• Global Exposure: Work with a multicultural team across multiple countries, with clients across the Life Sciences industry worldwide.
• Dynamic Work Environment: Join a young, enthusiastic team where your contributions are valued and your ideas shape the future of the company.
• Opportunities for Growth: A nurturing environment where your career can evolve well beyond your starting point.
• Drive Digital Transformation: Use the latest quality technologies to help organisations improve their processes and systems.

If you want to stand out, please send a motivation letter explaining why you are interested in Rephine, which QMS systems or software you have worked with and in what capacity, and your experience in Quality in the pharmaceutical industry: [e-mail]

About Rephine

With over 20 years of experience, Rephine continues to be a leader in quality management and GxP compliance for Life Sciences. Join us to deliver excellence, drive innovation, and make a global impact.