Global Quality Manager

Why AstraZeneca?

Join a team that supports the delivery of life-changing medicines for patients by enabling the rest of the business to run optimally and harness our progressive science. We're on a journey of growth and evolution. to find better ways to translate value for the business and our patients. We're always adapting and challenging the status quo, it's what helps us to succeed. But it's not change for change's sake. It's about working together seamlessly and inclusively, sharing ideas to find a better way. As a multi-cultural team, we are a winning combination of deep process knowledge, eye for business and hard work. We always go above and beyond for the collective good of the team. And with a deep personal connection to our patients, there's nowhere we'd rather be.

Ready to make a difference? Apply now!

Job Title: Global Quality Manager

Introduction to Role:
Join us as a Global Quality Manager in our Operations team, where you will be responsible for the enrolment, periodic verification, and removal of materials from the Certification program. This role is pivotal in ensuring compliance with Global quality management systems for the benefit of supply chain sustainability. You will also be responsible for key initiatives/projects in collaboration with global key partners of Supplier Quality, Quality Control, Quality Systems and Pharmaceutical Development that directly support execution of material Certification.

Accountabilities:
As a Global Quality Manager, your responsibilities will include authoring and reviewing Certification reports, supplier quality verification, deviation investigations, quality issue management and customer concern. You will maintain schedule adherence for all certification subprocesses, lead change control, SOPs, and LEAN initiatives to simplify and standardize processes. You will also be responsible for Quality Risk Assessment and collaborating with AZ Sites to achieve schedule adherence. Your role will also involve facilitating process and system improvements via voice of customer, archiving certification documentation as the need arises, and handling internal deviations in deviation system.

Essential Skills/Experience:

• Bachelor’s degree in a science / technical field such as Pharmacy, Biology, Chemistry or Engineering
• Strong proven knowledge of cGMPs, Quality Systems and the pharmaceutical supply chain environment.
• Strong understanding of industry standards such as Pharmacopoeia, ISO standards, etc.
• Excellent oral and written communication skills [English and local language(s)]
• Ability to work independently under their own initiative.
• Ability to travel nationally and internationally as required approximately 10% of their time.
• Desirable Skills/Experience:
• Multi-site / multi-functional experience
• - Confirmed experience in Quality Control

At AstraZeneca, we take Quality seriously. Our work is important and valued. We are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes. We are a team of ambitious people who want to go far. We are strong communicators and networkers. With constant exposure to different tasks we're at our best when we're working together as a team. We follow evidence to reach outcomes that benefit patients and AstraZeneca. Working on an immensely rich pipeline we adapt to get new medicines out quicker. Our focus is on scaling and introducing new technologies, using models to predict and proactively manage risk.

Join us! Be part of a team that works on diversified tasks with a global team. Work on multiple projects while partnering with knowledgeable colleagues across multiple business functions. Be exposed to new ways of thinking, helping us to grow collectively and as individuals. This is a place where you will feel included in the conversation. Every voice is heard and matters. Apply now!

📌Positions are open to Mexican Citizens and official residents of Mexico.
📍Location: Guadalajara (hybrid)
📌Strong Englishinterpersonal skills required.