Head of Quality Management / Global Supply Chain Pharma (f/m/d)

„Caring for People’s Health as a Trusted Partner“ – This mission motivates us at STADA every day to improve the health of people worldwide. With our wide range of generics, consumer health products and specialty pharmaceuticals, we offer patients, doctors and pharmacists a wide range of 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 Supply Chain (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 manufacturers, 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; knowledge of other languages is a plus.
• You are available to travel internationally as required.

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 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 website. At our website, 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 us. We will consider requests to work part-time on an individual basis. Please contact us in advance by e-mail and let us know how many hours per week you would like to work.

STADA Group promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology or sexual orientation. We use the strength of this diversity to develop creative ideas, expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation and the promotion of an inclusive working environment.

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