Local Patient Safety Lead

ROPU IMETA is a Regional Operating Unit consisting of 6 mid-sized Operating Units: India, Near East & UAE, Saudi Arabia, Gulf & East Africa (SAGEA), Türkiye, North East & West Africa, Southern Africa (South Africa & Sub Saharan Africa). Our strength lies in our exceptional talent and shared commitment to growing, developing, and retaining our people. Together, we collaborate to drive success and create lasting impact.

The Opportunity

We are hiring a Local Patient Safety Lead based in Dubai, UAE. The person responsible will lead the Near East & UAE Patient Safety & Pharmacovigilance function, driving local PV strategy, regulatory compliance, patient safety oversight, and continuous patient-focused improvements while serving as the Local QPPV and Health Authority contact.

The job holder will report to the Medical Director.

Responsibilities:

- Lead and develop the Near East & UAE Patient Safety & Pharmacovigilance (PSPV) team and define the local PSPV strategy based on the framework provided by global PSPV.

- Ensures the establishment and maintenance of a local pharmacovigilance (PV) system to safeguard patient's and clinical trial subject’s safety and public health in Near East & UAE in compliance with regulatory requirements and applicable internal procedures and processes.

- Ensures compliance with external requirements in line with the local PV legislation and applicable internal procedures and processes allowing the company to obtain and maintain marketing authorization of its products.

- Acts as local PV contact person/Local QPPV for the national Health Authority as legally required.

- Initiates, evaluates, implements and supports activities that are patient oriented and improve the status quo.

Requirements:

- Bachelor’s degree in Pharmacy; Doctor of Medicine/Dentistry

- 3 to 5 years of Pharmacovigilance experience

- Experience in the Gulf and Levant countries is a plus

- Holder of a valid UAE Professional Practice License or is eligible to obtain a UAE Professional Practice License.

- Knowledge of Boehringer Ingelheim’s therapeutic areas is a plus

Skills/Competencies

- Strong functional and technical expertise in Pharmacovigilance, including safety database management

- Excellent knowledge of applicable global, regional and local Pharmacovigilance regulations, relevant GxP requirements and patient safety relevant topics

- Proven experience with health authority interactions, inspections, audits, CAPA management, and inspection readiness

- Experience managing license partners, third-party vendors, and PV agreements (PVAs)

- Excellent leadership skills to manage a diverse team

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.