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Regulatory Affairs Specialist

We are IMETA

 

ROPU IMETA is a Regional Operating Unit 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 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 Position:

 

The Regulatory Affairs Specialist will be responsible for Regulatory Affairs activities for Tunisia and Algeria and will support regulatory systems and related tasks across the New Africa region, reporting to the Head of Regulatory Affairs New Africa – Animal Health.

This role will be based in Algeria, as a contracted position for 8 months only.

 

Key Responsibilities

  • Manage regulatory activities (registrations, variations, and renewals) for Tunisia and Algeria in compliance with local regulations and country launch plans.
  • Prepare, submit, follow up, and obtain approvals for new registrations, renewals, and variations.
  • Liaise with distributors, RA agents, and Health Authorities, including preparation of responses and submissions.
  • Support and maintain RA systems, databases, and trackers for Tunisia and Algeria, ensuring data accuracy and timely updates, and provide additional RA support for the New Africa region as required.
  • Prepare and review artwork layouts and coordinate product information reviews with marketing, translators, and partners.
  • Review and validate promotional and marketing materials to ensure alignment with the approved SPC.
  • Ensure proper archiving of regulatory documentation.
  • Support PV‑related activities in coordination with the IMETA PV Manager and technical teams.

Requirements

  • Bachelor’s degree in Veterinary Medicine or Life Sciences.
  • Minimum 2 years of experience in Regulatory Affairs (human or animal health).
  • Experience in preparation of registration, renewal, and variation dossiers.
  • Fluency in English, French, and Arabic.

Competencies

  • Planning, organization, and coordination skills.
  • Strong accountability and results‑oriented mindset.
  • Strong written and verbal communication skills.
  • Analytical and problem‑solving skills.
  • Time management skills.
  • Ability to work cross‑functionally in a regional environment.

 

 

What happens Next?

 

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

 

SPL 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.

 

Apply now »