Auf einen Blick
- Aufgaben: Lead global quality supply chain, ensuring compliance and batch release efficiency.
- Arbeitgeber: STADA is a trusted partner in healthcare, offering generics and specialty pharmaceuticals worldwide.
- Mitarbeitervorteile: Enjoy flexible hours, mobile work options, childcare allowance, and health-promoting offers.
- Warum dieser Job: Join a dynamic team focused on improving global health and driving innovation.
- Gewünschte Qualifikationen: Must have a degree in Pharmacy or related field, QP qualified, and 10+ years in quality assurance.
- Andere Informationen: Diversity is valued; part-time requests considered.
Das voraussichtliche Gehalt liegt zwischen 72000 - 100000 € pro Jahr.
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) 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 guidelines, 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 site, 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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Head of Global Quality Supply Chain / QP Pharma (f/m/d) Arbeitgeber: Stada Arzneimittel AG
Kontaktperson:
Stada Arzneimittel AG HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Head of Global Quality Supply Chain / QP Pharma (f/m/d)
✨Tip Number 1
Make sure to highlight your extensive experience in quality assurance and compliance within the pharmaceutical industry during your conversations. This role requires over 10 years of relevant experience, so be prepared to discuss specific examples of how you've successfully managed batch releases and ensured regulatory compliance.
✨Tip Number 2
Demonstrate your leadership skills by sharing instances where you've led diverse teams or managed cross-functional projects. STADA values strong team management, so showcasing your ability to mentor and align team roles will set you apart.
✨Tip Number 3
Familiarize yourself with STADA's corporate culture and values, such as Integrity, Entrepreneurship, Agility, and One STADA. Being able to articulate how your personal values align with theirs can make a significant impact during discussions.
✨Tip Number 4
Prepare to discuss your knowledge of global regulatory requirements, especially those related to EMA and FDA. Being well-versed in GMP, GxP, and ICH guidelines will demonstrate your technical expertise and readiness for this role.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Head of Global Quality Supply Chain / QP Pharma (f/m/d)
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Head of Global Quality Supply Chain position. Highlight key responsibilities and required qualifications that align with your experience.
Tailor Your CV: Customize your CV to reflect your relevant experience in quality assurance, compliance, and batch release within the pharmaceutical industry. Emphasize your QP qualification and any leadership roles you've held.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for improving health and your alignment with STADA's values. Mention specific examples of how you've led teams and improved processes in previous roles.
Highlight International Experience: If you have international experience or language skills, be sure to mention them. This is particularly important for a role that requires collaboration across global teams.
Wie du dich auf ein Vorstellungsgespräch bei Stada Arzneimittel AG vorbereitest
✨Showcase Your Expertise
Make sure to highlight your extensive experience in quality assurance and compliance within the pharmaceutical industry. Be prepared to discuss specific examples of how you've ensured GMP compliance and managed batch releases effectively.
✨Demonstrate Leadership Skills
As a candidate for a leadership position, it's crucial to illustrate your team management abilities. Share experiences where you successfully led cross-functional teams and promoted continuous improvement within your organization.
✨Understand Regulatory Requirements
Familiarize yourself with the relevant regulations, such as the European Union legislation and ICH guidelines. Be ready to discuss how you have navigated these regulations in past roles and how you plan to ensure compliance at STADA.
✨Communicate Effectively
Effective communication is key in this role. Prepare to explain how you facilitate smooth communication between stakeholders during the batch release process and how you handle quality events. Highlight any experience you have in automating processes to enhance efficiency.