Associate Director Quality & Compliance

TAPI; Lerma de Villada; Híbrido; MXN 60,000 - 100,000; Jornada completa

Descripción de la vacante

Ein innovatives Unternehmen in der pharmazeutischen Industrie sucht einen Qualitätsleiter, der die höchsten Standards in der Produktqualität sicherstellt. In dieser Schlüsselrolle sind Sie verantwortlich für die Einhaltung von Vorschriften und die Förderung einer Kultur der kontinuierlichen Verbesserung. Mit über 10-15 Jahren Erfahrung in der API-Herstellung und cGMP bringen Sie nicht nur technisches Know-how mit, sondern auch die Fähigkeit, Teams zu inspirieren und zu führen. Freuen Sie sich auf ein unterstützendes Arbeitsumfeld, das Flexibilität und berufliche Entwicklung fördert. Wenn Sie bereit sind, einen Unterschied zu machen, ist dies Ihre Chance.

Servicios

Flexible Arbeitszeiten

Umfangreiche Gesundheitsversorgung

Wohlfühlprogramme

Ausbildung und Schulungen

Großzügige Urlaubstage

Formación

• 10-15 Jahre Erfahrung in der pharmazeutischen Industrie, insbesondere in der API-Herstellung.
• Starke Kenntnisse der globalen GMP-Vorschriften und deren Umsetzung.

Responsabilidades

• Sicherstellen, dass alle Produkte den höchsten Qualitätsstandards entsprechen.
• Führen von Inspektionen und Zusammenarbeit mit Teams zur Qualitätssicherung.

Conocimientos

Qualitätsmanagement

cGMP Kenntnisse

Risikomanagement

Kommunikationsfähigkeiten

Problem-Lösungsfähigkeiten

Educación

Bachelor in Pharmazie

Master in Pharmakologie

Herramientas

Qualitätsmanagementsysteme

GMP-Compliance-Tools

Descripción del empleo

Company Description

At 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, as well as custom CDMO services, 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.

Job Description

Your Mission: Excellence in Every Molecule

In this role, you’ll be the guardian of our quality standards, ensuring that every product that leaves TAPI meets the highest quality and 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.

What Success Looks Like

Imagine yourself leading the charge in inspection readiness, navigating the complexities of global compliance, and ensuring our sites remain models of excellence and meeting highest standards. 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 quality compliance and quality culture.
• Sharing insights and best practices from inspections to strengthen our collective knowledge.
• Driving excellence in Quality KPis, DI Metrics, investigations and CAPA effectiveness.
• Current know how on global GMP regulations and their implementation ( Eg; COFEPRIS, FDA, EDQM,PIC/S etc) to add value to the quality systems/compliance programs.
  
  

Your impact will be felt far beyond the production line—ultimately reaching the patients whose lives depend on our products.

Who We’re Looking For

We’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 10-15 years of experience in the industry, including expertise in 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.

Why TAPI? Because We Care.

At TAPI, We Recognize That Our People Are Our Greatest Asset. That’s Why We’ve Created a Workplace Where You Can Thrive Both Professionally And Personally. Here’s What You Can Look Forward To

Growth Opportunities: Access to training, workshops, and tuition assistance to advance your career.

• Work-Life Balance: Flexible hours and hybrid work options so you can prioritize what matters most.
• Generous Time Off: Recharge with ample vacation days, holidays, and sick leave.
• Health & Wellness: Comprehensive health insurance, wellness programs, and fitness stipends to support your well-being.
• Supportive Culture: A diverse, inclusive, and collaborative environment where every voice is valued.
  
  

Additional Information

Make Your Mark with TAPI

Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!