Compliance Specialist

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.

The Opportunity

The Compliance Specialist is responsible for supporting and maintaining the site’s and organization’s state of regulatory compliance in accordance with GMP and global quality standards. This role plays a critical part in regulatory inspections, audit readiness, CAPA management, vendor oversight, and global compliance communications. The Compliance Specialist works closely with internal sites, external suppliers, and global quality stakeholders to ensure continuous inspection readiness and effective quality system performance.

How You’ll Spend Your Day

• Supporting regulatory authority inspections and external audits by preparing documentation, coordinating responses, and following up on observations
• Managing and tracking CAPA plans, ensuring actions are implemented on time and effectiveness is verified
• Supporting continuous inspection readiness by reviewing compliance status and addressing gaps proactively
• Planning, coordinating, and participating in scheduled or event driven internal compliance audits
• Reviewing quality performance metrics and helping to develop and track corrective and improvement action plans
• Monitoring regulatory updates and quality system changes and communicating relevant information to management
• Supporting global compliance knowledge management and maintaining compliance related documentation
• Working closely with internal sites and external GMP suppliers on compliance topics and quality requirements
• Supporting vendor audits, Quality Technical Agreements (QTAs), deviation investigations, and change control activities
• Reviewing, maintaining, and updating the Site Master File as required

Your experience and qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, Chemistry, Biology, or a related scientific discipline
• Minimum 2-year experience working in Quality Assurance, Compliance, or Regulatory roles within a GMP regulated environment
• Ability to simplify processes, identify bottlenecks and translate stakeholder feedback into clear processes
• Active listener and decision-making skills
• Team role player with strong analytical and critical thinking approach
• Knowledge of OPEX and implementation of time management tools (i.e. Daily Tier meetings, workplan boards)
• Hands on experience supporting regulatory authority inspections and external or internal audits
• Practical knowledge of CAPA management, including investigation follow up and effectiveness checks
• Good understanding of GMP principles, quality systems, and regulatory requirements (e.g., EMA, FDA, ICH)
• Experience working with suppliers or vendors, including audits, deviation investigations, or change controls
• Familiarity with Quality Technical Agreements (QTAs) and Site Master File maintenance is an advantage
• Ability to review quality performance data and support development of improvement action plans
• Strong documentation, organizational, and communication skills
• Ability to work independently, manage multiple priorities, and collaborate effectively with cross functional and global teams
• Ability to work independently while collaborating effectively with cross functional teams
• Fluent verbal and written communication skills in English

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. 

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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.