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Regulatory Affairs Executive

Boehringer Ingelheim
Riyadh, منطقة الرياض
دوام كامل
منذ أسبوع

We are IMETA

ROPU IMETA is a Regional Operating Unit of Boehringer Ingelheim consisting of 6 mid-sized Operating Units: India, Turkey, Southern Africa (South Africa & Sub Sahara Africa) Northeast & West Africa, Near East & UAE, Saudi Arabia, Gulf & East Africa (SAGEA).

IMETA is home to more than 47 nationalities. We are a myriad of color and culture and embracing this diversity is one of our greatest opportunities.

We are a powerhouse of talent, and we work together to ensure that we grow, nurture, and retain our talent. Uniting and working together is the key to our success.

The Opportunity

We are hiring a Regulatory Affairs Executive for the SAGEA OPU, based in Riyadh, Saudi Arabia . The successful candidate will be responsible for executing the local regulatory affairs activities to support the local and regional RA strategies and business priorities.

The Regulatory Affairs Executive will report to the SAGEA Head of Regulatory Affairs. The SAGEA region includes Saudi Arabia, Gulf countries and East Africa.

Tasks and Responsibilities:

  • Timely and qualitative execution of regulatory activities.
  • Compilation of dossiers, maintain product registrations and RA databases, ensuring business continuity in compliance with internal and external regulations and requirements.
  • Provide regular regulatory intelligence on changes in regulatory environment, competitor activity to enable the business to realize any risks or opportunities arising in the RA environment.
  • Collaborate cross-functionally and ensure relevant stakeholders are timely and pro-actively updated on relevant RA topics.
  • Have a strong interaction and partnership with the assigned authorities across the OPU/cluster, and maintain efficient relationships with related Regulatory service Providers (local agents and vendors).
  • Carry out agreed actions for the assigned local projects.

Requirements:

  • Graduate in Pharmaceutical Science or related studies.
  • Minimum 2 – 4 years working experience in Regulatory Affairs for Pharma companies
  • Experience networking directly with health and regulatory authorities in Saudi Arabia and Gulf countries.
  • Business fluent in English and Arabic.
  • Saudi National is a must.

Skills and Capabilities:

  • Critical thinking
  • Cross functional collaboration
  • Accountability and ownership
  • Effective negotiation and Communication
  • Agility to changes.

Our differences are our strengths. A global collective. Waiting for you.

What’s Next?

We are looking forward to receiving your application! We will then have a look at your profile. If we see a match, we will invite you for a screening interview.

Screening:

In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (“SPL”). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.

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