Head of Global Quality EU Release (f/m/d) (Leiter/in - Qualitätsmanagement)

وصف الوظيفة

 
therapeutic options.

Around 11,700 employees live our values of Integrity, Entrepreneurship,
Agility and One STADA. Together we are on an exciting growth journey and
want to successfully shape the future of STADA.

Do you want to become part of a dynamic, international team and grow with
us? Then apply now as:

Head of Global Quality EU Release (f/m/d) * *

Bad Vilbel | Germany (DE) | Full-time | Permanent | Quality | Management /
Executives

What you can expect

As Head of Global Quality Supply Chain, you will oversee batch release
quality and compliance across internal sites and third-party maufacturers,
ensuring all products (pharmaceutical and non-pharmaceutical products) meet
global standards and align with the company’s Quality Management System.

· You lead and mentor a diverse team, ensuring role alignment and process
efficiency, while promoting continuous improvement
· You oversee the batch release process, ensuring all releases comply with
GMP and meet regulatory and internal standards
· You coordinate batch releases by facilitating smooth communication
between stakeholders and ensuring thorough review and approval of product
testing, packaging, and GMP documentation for all products
· You collaborate with Compliance Team Leads, QPs, the release
coordinator, and Supply Chain to manage quality events and ensure timely
batch releases that meet market demands and supply chain priorities
· You enhance global batch release efficiency through automation, aligning
team tasks for seamless operations and cost reduction
· You ensure regulatory compliance, manage deviations, and address audit
findings, especially for batch releases
· You manage budgets, optimize resources, and streamline operations to
meet financial objectives

-Who we are looking for-

· You have a university degree in Pharmacy, Chemistry, Life Sciences, or a
related field
· You are QP qualified according to § 15 AMG and aligned with European
Union legislation, particularly Directive 2001/83/EC
· You possess over 10 years of experience in quality assurance,
compliance, and batch release within the pharmaceutical industry
· You have in-depth knowledge of GMP, GxP, ICH guideline, and global
regulatory requirements in EMA and FDA regulated countries
· You demonstrate strong leadership and team management skills, with
experience managing global and cross-functional teams
· You combine technical expertise with business vision and a strong
customer orientation
· You are proficient in English and German; knowledge of other languages
is a plus
· You are available to travel internationally as required
· Please submit your CV in English

-What we offer-

· An open corporate culture with fast decision-making processes and a lot
of potential for your personal development
· Individual development and training opportunities
· Flexible working hours and mobile working up to 2 days per week
(depending on the job profile)
· Job ticket for the RMV region and Job Bike
· Childcare allowance
· Health-promoting offers such as or the STADA Gym (free of charge)
· Numerous additional benefits such as group accident insurance or
supplementary pension scheme
· Subsidized cafeteria

We look forward to receiving your application via our . At <a href="http://jobs.stada.com" target="_blank" rel="nofollow">jobs.stada.com</a>
you will also find numerous other job opportunities, as we are always
looking for motivated talents who can strengthen our team with their
expertise and personality. Do you have further questions? Then please reach
out to . We will consider requests to work part-time on an individual
basis. Please contact us in advance by e-mail (<a href="mailto:[email protected]" rel="nofollow">[email protected]</a>) and let
us know how many hours per week you would like to work.