At a Glance
- Tasks: Lead the global Quality Management System and ensure compliance across all operations.
- Company: Join Teva, a leading biopharmaceutical company focused on innovation and patient care.
- Benefits: Enjoy a competitive salary, flexible work options, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by driving quality and compliance in a global setting.
- Qualifications: 15+ years in pharma quality roles, with strong leadership and regulatory knowledge.
- Other info: Be part of an inclusive culture that values collaboration and fresh ideas.
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. The 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. This role is also 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
- 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.
- Core QMS Processes Ownership: Provide global oversight and accountability for key QMS processes, including Change Control, Deviations, Investigations, CAPA, Document and Records Management, Training and Learning Management, Quality Risk Management, Complaint Handling, and Product Quality Surveillance.
- 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.
- QMS Modernization & Continuous Improvement: Ensure the QMS evolves to support new operating models, technologies, and business strategies without compromising compliance.
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, SDLC compliance, and data integrity.
- 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.
- Provide coaching, leadership, and development to regional quality system owners and IT quality professionals.
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.
- Expert knowledge and understanding of cGMP, Risk Management, and in the implementation of Pharmaceutical Quality Management Systems.
- Strong critical thinking/problem-solving skills; Strategic thinking; Excellent storytelling and presentation skills; Cross-functional collaboration and stakeholder management.
We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration.
Head of Global Quality Management Systems and IT Quality Compliance in Port Talbot employer: Teva Pharmaceuticals
Contact Detail:
Teva Pharmaceuticals Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Head of Global Quality Management Systems and IT Quality Compliance in Port Talbot
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals 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 showcase how you can contribute to their mission.
✨Tip Number 3
Practice your storytelling skills! Be ready to share your experiences and achievements in a way that highlights your fit for the role. We suggest using the STAR method (Situation, Task, Action, Result) to structure your responses effectively.
✨Tip Number 4
Don’t forget to follow up after your interviews! A simple thank-you email can go a long way in leaving a positive impression. We believe this shows your enthusiasm for the role and keeps you top of mind for the hiring team.
We think you need these skills to ace Head of Global Quality Management Systems and IT Quality Compliance in Port Talbot
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. Use keywords from the job description to show that you understand what we’re looking for.
Showcase Your Leadership Skills: Since this is a leadership role, don’t forget to emphasise your experience in leading teams and driving change. Share specific examples of how you've developed others and managed complex projects in your previous roles.
Be Clear and Concise: When writing your application, keep it clear and to the point. We appreciate well-structured applications that get straight to the heart of your qualifications and experiences without unnecessary fluff.
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 and shows us you’re serious about joining our team at Teva.
How to prepare for a job interview at Teva Pharmaceuticals
✨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 help you demonstrate your expertise and show that you're ready to take on the leadership role.
✨Showcase Your Leadership Skills
Prepare examples of how you've successfully led teams in previous roles, especially in a GMP environment. Highlight your experience in managing change, driving transformation, and fostering a culture of accountability. Be ready to discuss how you can lead the global Quality Systems and IT Quality organisation effectively.
✨Be Ready for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills and strategic thinking. Think about potential challenges in quality management and compliance, and prepare to discuss how you would approach these situations. This will showcase your critical thinking and ability to navigate complex environments.
✨Engage with Cross-Functional Collaboration
Since this role involves working across various functions like R&D, IT, and Regulatory Affairs, be prepared to discuss your experience in cross-functional collaboration. Share specific examples of how you've successfully aligned different teams towards common goals, as this will highlight your stakeholder management capabilities.