You will have the opportunity to:

• Lead investigations for deviations and complaints, ensuring timely root cause analysis and effective CAPA implementation.
• Coordinate and monitor change control processes, ensuring compliance and timely execution of change plans.
• Review and approve manufacturing batch records and local documentation in alignment with GxP and quality system requirements.
• Participate in internal audits, external inspections, and compliance gap assessments, escalating risks as needed.
• Monitor quality system performance indicators, support training oversight, and follow up on validation, maintenance, and calibration activities.

We promise you will own your success.We will empower you with the freedom and autonomy to shape your work, make key decisions, and take ownership of your success. We will trust you to lead, innovate, and make an impact from day one.
And we will also bring you:

• A collaborative and inclusive work environment where your voice matters.
• Opportunities to grow within a leading pharmaceutical company committed to innovation and excellence.
• Exposure to cross-functional projects and international teams.
• A culture that values continuous learning, development, and recognition.