Associate Director Quality And Compliance (Sme) - Tapi Rho

Associate Director Quality And Compliance (Sme) - Tapi
Rho
Lombardia, Rho

Join TAPIAt TAPI, we're not just a company—we're a community committed to advancing health from the core.

As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies.

With a legacy spanning over 80 years and a portfolio of more than 350 products, we're shaping the future of health worldwide. Our strength lies in our people—a team of over 4, 200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India.

Together, we innovate, solve problems, and deliver excellence.

Join us, and be part of a mission that transforms lives. Location of the positionThis position is available in Rho (IT), Zagreb (CRO), Debrecen (HUN) or Opava (CZ)Your missionIn this role, you'll be the guardian of our quality standards, ensuring that every product that leaves TAPI meets the highest quality & compliance benchmarks.

You will not only influence operations across our manufacturing and R&D sites but also play a pivotal role in upholding trust with regulators and patients alike. Your expertise will touch every corner of our operations, from maintaining compliance and managing quality risks to fostering a culture of continuous improvement.

By working closely with cross-functional teams—from Manufacturing Science & Technology to Regulatory Affairs—you'll help set the gold standard in quality/compliance for the industry. How you'll spend your dayImagine yourself leading the charge in inspection readiness, navigating the complexities of global quality systems, and ensuring our sites remain models of excellence.

You'll be at the forefront of cutting-edge initiatives like: • Preparing sites for health authority inspections and collaborating with teams to ensure a seamless process. • Championing quality risk management systems to safeguard product integrity. • Driving global projects that enhance compliance and reduce deviations. • Sharing insights and best practices from inspections to strengthen our collective knowledge.

Your impact will be felt far beyond the production line—ultimately reaching the patients whose lives depend on our products. Who We're Looking ForWe're seeking a leader with a passion for quality and a deep understanding of pharmaceuticals manufacturing.

You're someone who thrives in complex environments and sees challenges as opportunities to innovate and improve.

With over 15 years of experience in the industry, including expertise in sterile API processes and cGMP, you're ready to make a difference.

You bring not only technical expertise but also the ability to inspire and influence others.

Whether it's preparing teams for inspections or leading a global project, your communication and problem-solving skills set you apart.

You're a natural collaborator who can navigate matrix environments, driving change while building trust. Contact personVincent van Straten - Head of Talent Acquisition