Career Opportunities: Quality Assurance Auditor (68928)

Requisition ID 68928 - Posted  - Argentina

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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

This section is where we attract the attention of potential candidates and sell the role. How has the role come about? What makes it appealing? What are the key responsibilities? How is the role better with Teva than with another company? Wherever possible, we should bring through the essence of our EVP pillars, i.e., we care, we’re in it together, and we make work fulfilling.

How You’ll Spend Your Day

• Lead and manage the site's internal, external, and supplier audit programs, ensuring compliance with GMP regulations, corporate quality standards, and applicable health authority requirements.
• Develop, coordinate, and monitor the annual audit plan, including the organization of cross-functional audit teams and follow-up of corrective and preventive actions (CAPAs).
• Drive continuous improvement initiatives by assessing compliance with cGMP requirements, identifying risks and improvement opportunities, and partnering with functional teams to implement corrective actions.
• Ensure audit readiness across the site by maintaining effective audit systems, procedures, and inspection preparedness programs.
• Conduct supplier and third-party audits as part of qualification and approval processes, ensuring vendors meet GMP requirements, quality agreements, and company expectations.
• Prepare, maintain, and update audit-related procedures in alignment with corporate quality policies and global regulatory requirements.
• Support Regulatory Affairs and regional quality teams by providing audit documentation, supplier compliance data, and quality-related information for product registrations and regulatory requests.
• Monitor and report quality compliance metrics and KPIs while supporting a culture of quality, compliance, and continuous improvement throughout the organization

Your Skills and Experience

• Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Engineering, or another relevant scientific or technical discipline.
• 3-5 years of experience in the pharmaceutical industry or other regulated manufacturing environments.
• Experience in Quality Assurance, Quality Control, Manufacturing, or Quality Systems, including process controls and documentation management.Strong knowledge of GMP/cGMP requirements and pharmaceutical quality systems.
• Understanding of pharmaceutical regulations and health authority requirements, including ANMAT and international regulatory standards.
• Experience performing audits, assessing compliance risks, and managing CAPA activities.
• Strong analytical, organizational, and problem-solving skills with attention to detail.
• Effective communication and stakeholder management skills, with the ability to work across multiple functions.
• Proficiency in SAP, Microsoft Office applications and quality documentation systems.
• Intermediate to advanced English proficiency.

Also Good to Have

• Experience conducting supplier, contract manufacturer, or third-party audits.Knowledge of global pharmaceutical regulations and inspection practices from international health authorities.
• Familiarity with supplier qualification programs, quality agreements, and vendor management processes.
• Experience supporting regulatory inspections, submissions, and audit readiness initiatives.
• Understanding of Environment, Health & Safety (EHS) requirements within a manufacturing environment.
• Lead Auditor certification or formal audit training.
• Proven ability to influence cross-functional stakeholders and drive continuous improvement projects.
• Experience working in multinational pharmaceutical organizations and global quality compliance programs.

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?

Make sure to apply through our internal career site on Twist—your one-stop shop for career development

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.

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