At a Glance
- Tasks: Lead the global Quality Management System and ensure compliance across all operations.
- Company: Teva, a leading innovative biopharmaceutical company with a collaborative culture.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Join a high-performing team that values fresh ideas and fosters an inclusive workplace.
- Why this job: Make a real impact on global health while driving quality and compliance in a dynamic environment.
- Qualifications: 15+ years in pharmaceutical quality roles, with strong leadership and strategic thinking skills.
The predicted salary is between 100000 - 130000 € per year.
The Head of Global Quality Management Systems and IT Quality Compliance is a key leadership role, with primary accountability for the strategy, design, governance, and execution of the Teva Global Quality Management System (QMS) across all manufacturing sites and markets. This role is responsible for managing the development, implementation, and continuous improvement of the Teva Global Quality System, ensuring that quality processes, standards, and systems are harmonized, scalable, and consistently executed across the enterprise.
The position serves as the global process owner for the Quality Systems Management program, ensuring the QMS remains fit for purpose, inspection-ready, and aligned with evolving regulatory expectations and business needs. In parallel, this role is the enterprise Quality authority for IT Quality Compliance, accountable for the governance, compliance strategy, and risk management of computerized systems that support regulated business processes.
The role ensures that digital and computerized systems are fully integrated into the QMS, compliant with global GxP requirements, data integrity principles, and regulatory expectations, enabling compliant, efficient, and future-ready operations. Operating with significant autonomy, this position owns enterprise-level quality system and IT compliance risk, inspection outcomes, and organizational capability related to Quality Systems and IT Quality.
The role works cross-functionally with Quality, Manufacturing, Supply Chain, R&D, IT, and Regulatory Affairs to drive alignment, execution, and continuous improvement across the global quality ecosystem.
How You’ll Spend Your Day
- Responsible for leading and governing the following core elements of the Global Quality Systems Management program:
- Global QMS Strategy & Governance - Define and execute the global QMS strategy, ensuring alignment with corporate Quality objectives, regulatory requirements, and business priorities. Establish and maintain global Quality policies, standards, and frameworks as part of the enterprise QMS. Ensure clear process ownership, governance, and accountability across all QMS elements.
- Core QMS Processes Ownership - Quality Metrics and KPI development and implementation. Provide global oversight and accountability for key QMS processes, including Change Control, Deviations, Investigations, and CAPA, Document and Records Management, Training and Learning Management, and Quality Risk Management activities.
- QMS Performance, Compliance & Inspection Readiness - Ensure the Global QMS supports continuous inspection readiness and effective regulatory compliance; Monitor QMS performance, trends, and health metrics to proactively identify and mitigate systemic risk; Sponsor and lead remediation and transformation initiatives to address systemic quality or compliance gaps.
- QMS Modernization & Continuous Improvement - Ensure the QMS evolves to support new operating models, technologies, and business strategies without compromising compliance; Drive QMS simplification, standardization, and modernization through digital enablement and automation.
Key Responsibilities – IT Quality Compliance (Integrated Accountability)
- Own the global IT Quality Compliance framework, fully embedded within the Global QMS. Provide enterprise governance and oversight for computerized systems validation (CSV), SDLC compliance, and data integrity.
- Ensure IT systems supporting regulated processes are fit for intended use, compliant by design, and inspection-ready. Provide executive leadership for IT-related audits, inspections, deviations, and critical quality events.
- Guide compliance approaches for cloud platforms, SaaS solutions, automation, AI/ML, and emerging digital technologies.
Leadership & Enterprise Accountability
- Lead and develop a global Quality Systems and IT Quality organization, including senior leaders and subject-matter experts. Act as a trusted advisor to Global Quality, IT, and business executives.
- Own enterprise risk and inspection outcomes related to Quality Systems and IT Quality Compliance. Balance regulatory rigor, operational efficiency, and innovation while maintaining Quality independence.
- Provide coaching, leadership, and development to regional quality system owners and IT quality professionals. Lead transformation programs focused on digitization, simplification, and standardization of global processes.
- Lead, mentor, and develop a high-performing global team, promoting collaboration and innovation, fostering a culture of accountability, professional growth, and employee engagement.
Qualifications
- BS Degree in Science, Life Sciences, Engineering, Pharmacy or related.
- Minimum of 15 years' pharmaceutical experience in a Quality or Operations role in a GMP environment in a large pharma company.
- At least 5 years in leading direct reports in a site Quality unit, Quality operation and Quality Control.
- Expert knowledge and understanding of cGMP, Risk Management, and in the implementation of Pharmaceutical Quality Management Systems.
- Expert knowledge in regulatory standards in Pharmaceutical Industry, including requirements and expectations of global regulatory bodies, particularly US FDA and EU authorities.
- Practical knowledge of Global Compliance and Regulatory requirements, Industry, cGxP and associated guidelines, Quality System, IT quality compliance and Risk Management.
- Direct interaction with health authorities.
- Experience working in a large, complex matrixed environment with global processes & governance structures; practical knowledge of pharmaceuticals and R&D.
- Practical knowledge on risk management.
Essential Skills
- Strong critical thinking/problem-solving skills to navigate ambiguous situations; Strategic thinking; Excellent storytelling and presentation skills; Cross-functional collaboration and stakeholder management; Effective communication; Strong relationship and senior stakeholder management capabilities.
- Strong leadership, change management & influencing skills; Decision-making under uncertainty skills; Ability to drive transformational change in a large/global/matrixed environment; Proven talent management & people development capabilities (incl. coaching and mentoring); Ability to create an engaging & inclusive work climate and a culture of appreciation and trust; Ability to set a vision and drive organizational change and innovation; Ability to manage effectively complexity within the organization (shifting timelines, projects, priorities).
We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You’ll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
Head of Global Quality Management Systems and IT Quality Compliance in Street employer: Teva Nederland
Teva is an exceptional employer, offering a dynamic and inclusive work culture that prioritises collaboration and innovation. As the Head of Global Quality Management Systems and IT Quality Compliance, you will have the opportunity to lead a high-performing team while driving meaningful change in a global biopharmaceutical environment. With a strong focus on employee growth and development, Teva provides the flexibility to balance work and life, ensuring that you can thrive both personally and professionally.
StudySmarter Expert Advice🤫
We think this is how you could land Head of Global Quality Management Systems and IT Quality Compliance in Street
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their values and how they align with your own. We want you to walk into that interview feeling confident and ready to show them why you’re the perfect fit!
✨Tip Number 3
Practice your storytelling skills! Be ready to share your experiences and achievements in a way that highlights your skills and how they relate to the role. We believe that a good story can make you memorable to interviewers.
✨Tip Number 4
Don’t forget to follow up after your interviews! A simple thank-you email can go a long way in showing your appreciation and keeping you top of mind. We’re all about making those connections last!
We think you need these skills to ace Head of Global Quality Management Systems and IT Quality Compliance in Street
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience in Quality Management Systems and IT Quality Compliance. We want to see how your skills align with the role, so don’t hold back on showcasing relevant achievements!
Showcase Your Leadership Skills:As this is a leadership role, it’s crucial to demonstrate your ability to lead teams and drive change. Share examples of how you've successfully managed teams or projects in the past, especially in complex environments.
Be Clear and Concise:When writing your application, keep it clear and to the point. Use bullet points where possible to make it easy for us to read through your qualifications and experiences. We appreciate straightforward communication!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details you need about the role and our company culture there!
How to prepare for a job interview at Teva Nederland
✨Know Your QMS Inside Out
Before the interview, make sure you thoroughly understand the Teva Global Quality Management System. Familiarise yourself with its core processes, governance structures, and how it aligns with regulatory requirements. This will not only show your expertise but also demonstrate your commitment to the role.
✨Showcase Your Leadership Skills
As a Head of Global Quality Management Systems, you'll need to lead a diverse team. Prepare examples of how you've successfully managed teams in the past, focusing on your ability to drive change and foster collaboration. Highlight any specific initiatives where you’ve improved quality compliance or operational efficiency.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in ambiguous situations. Think of scenarios where you've had to navigate complex regulatory challenges or implement quality improvements. Be ready to discuss your thought process and the outcomes of your decisions.
✨Engage with Cross-Functional Collaboration
This role requires working closely with various departments like R&D, IT, and Regulatory Affairs. Prepare to discuss how you've effectively collaborated across functions in previous roles. Share specific examples of how you’ve built relationships and aligned objectives to achieve common goals.
