QPPV / Qualified Person Responsible for Pharmacovigilance in Heidenheim an der Brenz bei THE FORCE CT GmbH

Location: one of our offices in Heidenheim an der Brenz/Berlin (Germany) or remote (willingness to relocate to Germany preferable)

Starting: at the next possible date

ABOUT THE FORCE:

THE FORCE builds companies for companies in the healthcare and pharmaceutical sector.

We encourage work in a flexible surrounding and as a diverse group when it comes to gender, nationality, religion, and ways of working. This unique culture is aimed to integrate employees and partners seamlessly into one organization.

Likewise, this organization shall easily adapt to customer organizations. Our unique way of operation will release THE FORCE to solve customer problems in a fast, effective, and efficient manner.

PEOPLE ARE OUR STRENGTH:

In all of this, people are and will be at the center of our attention, and the most valuable asset we have: People are our strength. They make us THE FORCE.

For you, this means you are flexible in your working hours, your location, and your work itself. You will also have a big say in what exactly you and we are aiming for. But above all, we are interested in you as a person and focus on your specific talents. We are looking for that certain something – and will give it to you in return.

WHAT ARE WE SEARCHING FOR?

In a growing company, we are looking for people who don’t feel like a fish out of water in new situations and with new customers.

Your current environment doesn’t feel like the best fit anymore? THE FORCE has the right biotope for you. We are searching for a professional with a passion in the field of medical sciences, medical affairs, or pharmacovigilance.

WHAT MAKES YOU FIT RIGHT IN?

• You have a medical degree and a keen interest in people.
• You want to work in the field of medical affairs, and it feels natural for you to interact and engage with players in the medical community.
• Your assets include an entrepreneurial spirit with a humble approach and the ability to influence and persuade stakeholders.
• Your medical knowledge qualifies you to provide medical judgement of the products we are developing as well as reported side effects.
• You are not deterred by taking on tasks that aren’t directly related to your specific role if the team needs you to support.
• You can ensure compliance with applicable local and global laws, regulations, and guidelines, and are willing to implement those in our and our customers’ processes and policies.
• Your proficiency in English and German are the cornerstone for effective communication both in our team and with customers.

WHAT WILL YOU CONTRIBUTE TO YOUR NEW ENVIRONMENT?

• You build all necessary PV systems and procedures to run effective PV activities for our clients.
• You dedicate time to keep up to date with new developments in the field of pharmacovigilance.
• You evaluate products for our customers from a medical point of view.
• You develop concepts in collaboration with the rest of the team on how best to support our customers within the medical community.
• In the launch phase, you use your skills to engage with key opinion leaders and convince them on behalf of our customers.
• After launch, you are a resource for customers looking for explanation, instructions, and guidance on how to use their products.