Qualified Person (QP) (Fixed-term contract)

We Are Teva

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.

Our Team, Your Impact

We are looking for an experienced Qualified Person (QP) to join our Quality organization and play a key role in safeguarding patient safety through oversight of GMP compliance, batch certification, and product release activities. This is an exciting opportunity to contribute to a highly regulated environment where quality and excellence are at the heart of everything we do.

What You'll Do

As a Qualified Person, you will be responsible for:

• Batch certification and release activities
• Oversight of GMP compliance across manufacturing and quality operations
• Review and approval of quality events, deviations, investigations, and CAPAs
• Supporting regulatory inspections and audit readiness
• Driving quality risk management initiatives
• Ensuring compliance with applicable regulatory requirements and quality standards
• Acting as a key quality partner for cross-functional teams and stakeholders

What You'll Bring

To be successful in this role, you will have:

• Strong GMP and regulatory expertise
• Solid experience within the pharmaceutical industry
• Hands-on experience with batch certification and product release
• In-depth knowledge of Quality Management Systems (QMS)
• Experience supporting inspections and regulatory audits
• Strong understanding of:
  • EU GMP requirements, including Annex 16
  • Validation and qualification processes
  • Deviations, investigations, and CAPA management
  • Data Integrity principles (ALCOA+)
  • Quality Risk Management (ICH Q9)
  • Regulatory compliance requirements
  • Batch release processes

What Makes You Stand Out

You are a quality-focused professional who combines technical expertise with sound judgment and strong decision-making skills. You bring:

• High accountability and integrity
• Exceptional attention to detail
• Strong analytical and problem-solving skills
• Resilience and the ability to perform under pressure
• A patient-focused mindset
• Leadership capabilities and confidence in decision-making

How We’ll Take Care of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.

Already Working @Teva?

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.