Regulatory Affairs Intern
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 Opportunity
We are looking for a motivated individual to join our Near East & UAE Regulatory Affairs team based in Amman, Jordan as an Regulatory Affairs Intern for 3 months.
Key responsibilities:
- Support the preparation and organization of product dossiers for eCTD baseline submissions
- Review approved regulatory documentation and verify completeness against approved records
- Retrieve, compile, index, and reconcile regulatory documents from internal databases and archives
- Assist in tracking dossier gaps and following up with internal stakeholders to obtain missing documents
- Support the review of documents prior to eCTD publishing activities
- Maintain submission trackers and project dashboards to monitor progress against timelines
- Coordinate with Regulatory Affairs colleagues to ensure documents are accurately filed and version-controlled
- Assist in preparing submission-related documentation, and supporting materials
- Participate in data entry, document QC, and metadata verification activities
Qualification:
- Recent graduate in Pharmacy or life sciences
- Basic understanding of pharmaceutical regulatory affairs
- Familiarity with CTD/eCTD structure is an advantage
- Strong analytical, organizational, and problem-solving abilities
- Willingness to learn and develop professionally
- Ability to manage projects and follow up effectively
- Capable of working independently and collaboratively
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.