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Regulatory Affairs Specialist

2 weeks ago


الرياض, Saudi Arabia MSD Full time

**Bring energy, knowledge, innovation to carry out the following**:
**(may not be limited to)**:

- For assigned products ensures high quality labelling translation and artwork management.
- Supports the agency interactions to ensure a seamless submission, assessment, and quick approval of the CTAs, according to the new regulations, in cooperation with other internal stakeholders.
- Stay updated on relevant EU and local regulations and guidelines.
- Collects relevant publicly available regulatory information (regulatory intelligence) and keeps relevant persons appropriately informed.
- Maintains a positive relationship with internal and external regulatory contacts on sub-regional, regional and global level, our Manufacturing Division, EUQPPV and GSC&PV are the main contact points within the company. External contacts are regulatory authorities, as well as other key players in the regulatory environment.

**What skills you will need**:
In order to excel in this role, you will more than likely have:

- Must hold a degree in pharmacy or other life science or equivalent. An approx. minimum of 1-2 years’ experience in the pharmaceutical Industry is preferable, in a regulatory, medical or laboratory position.
- Ability to communicate well verbally and in writing, good organizational and planning skills, a meticulous attention to detail and be flexible enough to successfully handle conflicting time pressures and a large volume of work
- A sound appreciation of the interactions and relationships with other groups internally, a client-oriented approach and work according to the company leadership vision

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Regular

**Relocation**:
**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
Not Applicable

**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Job Posting End Date**:
03/3/2025

**Requisition ID**:R336261