Senior Specialist Global Pharmacovigilance

**Job Description**:
We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

We are looking for a **Senior Specialist Global Pharmacovigilance (M/F/d) **to join our team in Schwabenheim. This position is a full-time, fix-term contract for 2 years.

**Major activities and responsibilities**:

- Case review/approval for assigned products
- Expedited case submission according to timelines outlined in applicable regulations
- Case entry for non-PV-Works countries for assigned products
- PV Statement and PSUR preparation in compliance with relevant regulations and policies
- Participation in signal management activities

**Requirements**:

- Knowledge of pharmacology /toxicology or practical veterinary experience of advantage
- Experience in a highly regulated pharmaceutical field, ideally pharmacovigilance or regulatory affairs of advantage
- Strong analytical, communication and writing skills
- Proficient in English

**Our Benefits**:

- Trustbased working hours (37.5 hours/week) and an attractive company pension scheme
- Competitive salary package: 13 monthly salaries + holiday pay (EUR 1,200 annually) + target bonus achievement
- 30 days holiday entitlement
- Hybrid working model
- Internal further training and promotion opportunities
- International cooperation
- On-the-job training
- Contribution of own ideas to the process design
- Insights into the development of veterinary medicinal products
- Corporate benefits and free (e-) parking spaces
- Good company canteen and a company health management system

Our Regulatory Affairs team brings new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world.

**Who we are **
We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

**What we look for **
Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Temporary (Fixed Term)

**Relocation**:
No relocation

**VISA Sponsorship**:
**Travel Requirements**:
10%

**Flexible Work Arrangements**:
Flex Time, Hybrid

**Shift**:
Not Indicated

**Valid Driving License**:
No

**Hazardous Material(s)**:
**Requisition ID**:R223328