Quality Assurance Specialist

hace 3 semanas


Ciudad de México, Ciudad de México Novo Nordisk AS A tiempo completo

Are you passionate about ensuring the safety and efficacy of pharmaceutical products? Do you have experience in pharmacovigilance and quality oversight? If so, you might be the perfect fit for our LATAM Quality & Pharmacovigilance Analyst position at Novo Nordisk A/S.

The Position

As a LATAM Quality & Pharmacovigilance Analyst, you will be responsible for overseeing the quality and pharmacovigilance compliance of external partners with quality or pharmacovigilance responsibilities. You will also be an active team member in assigned quality and pharmacovigilance regional projects, supporting the implementation of global projects in the region when appointed.

Key Responsibilities

  • Ensure compliance with regulatory requirements for new products and product amendments.
  • Participate in the resolution of any legal liability and comply with governmental regulations.
  • Oversee the quality and pharmacovigilance compliance of external partners.
  • Support the implementation of global projects in the region.

Qualifications

We are looking for a highly motivated and detail-oriented individual with a Bachelor's degree in life sciences or a related field. You should have proficiency in computer skills such as Excel and PowerPoint, as well as 1-2 years of experience in pharmacovigilance, administration, and follow-up of deadlines. Ability to analyze data, generate reports, and provide insights on compliance is also essential.

About the Department

This job family covers both Regulatory Affairs and Safety Pharmacovigilance. The Regulatory Affairs function ensures the organisation gains regulatory approval of clinical trial applications, new drugs, devices, and digital health, as well as expands the availability of existing products. The Safety Pharmacovigilance function works to safeguard patients by ensuring medicines are safe to use.



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