Quality and Compliance Graduate Program

Quality and Compliance Graduate Program - Spain

Looking for more than just a job? Join Sanofi Spain Graduate Programme – a 12-month journey combined with a university-accredited course – so you can learn, grow, and gain real experience at the same time.

When you apply, you’ll select a stream that matches your interests. From there, we’ll match you to a specific role within one of our teams, based on your strengths and current opportunities. You won’t rotate between roles – instead, you’ll join one team from day one, take real ownership, and contribute to projects that make an impact. From day one, you’ll work on meaningful projects, collaborate with diverse teams, and build skills that open doors across functions, countries, and careers. This isn’t about fitting into a role. It’s about growing into your potential.

What Makes This Programme Different

• You contribute from day one – it’s a full-time role.
• You study while you work (fully supported).
• You learn from people who genuinely want you to grow.
• You gain exposure to international teams and ways of working.

About Sanofi

By combining science, technology, and collaboration, we’re transforming healthcare – and creating opportunities for people like you to grow, learn, and make an impact from day one. Together, we chase the miracles of science to improve people’s lives.

Your Journey

Join teams that ensure our medicines and vaccines meet the highest quality, safety, and regulatory standards. You’ll work across quality systems, compliance, and regulatory processes that protect patients and uphold trust. Safeguard the quality and compliance of healthcare innovation.

What You’ll Gain

• Experience with GxP, deviations, CAPA, and quality documentation.
• Exposure to regulatory submissions and local/global compliance processes.
• Understanding of product lifecycle quality and risk management.
• Confidence working in a structured, regulated environment.

What You May Work With

• Quality systems dashboards & documentation tools
• SOPs/PNTs, change control systems
• Regulatory frameworks and reporting tools
• Supplier quality systems and audit processes

What You’ll Do

• Support quality systems: deviations, CAPA, change control, audits.
• Assist with regulatory submissions, post‑approval variations, and compliance checks.
• Contribute to product quality reviews (PQR) and supplier oversight.
• Prepare documentation, reports, and quality‑related SOPs.

This Could Be You If…

• You’re detail‑oriented and analytical.
• You care about doing things right, safely, and compliantly.
• You enjoy structured processes and documentation.
• You communicate clearly and work well across teams.

What You’ll Bring

You don’t need to have everything figured out – but you’ll likely thrive in this programme if you bring:

• A Bachelor’s or Master’s degree in a relevant field (completed within the last 3 years or graduating soon).
• Confidence working in English (B2 minimum, C1 preferred); Spanish is a plus.
• Curiosity, initiative, and a genuine interest in learning and growing.
• Strong communication skills and a collaborative mindset.
• A problem-solving approach and willingness to take on new challenges.
• Openness to combining work with a university-accredited course during the programme.

Before applying, a couple of practical things to keep in mind:

• You must have full right to work in Spain.
• You’ll be enrolled in a university-accredited course alongside your role.
• The programme starts on 1 October 2026 and requires a 12-month commitment.
• To support you, we offer a development package of up to €3,000 to help cover the cost of your studies.

And if you’re reading this thinking “I’m not sure I tick every box…” – that’s completely okay. If this opportunity excites you, we’d love to hear from you.

Key skills/competency

• Quality Systems
• Compliance
• Regulatory Affairs
• GxP
• CAPA
• Audits
• Documentation
• Risk Management
• Pharmaceutical Industry
• Problem Solving