Do you want to make a significant difference on a global scale?
Is your area of expertise Good Pharmacovigilance Practice (GVP) and pharmacovigilance processes? If you at the same time are looking for a job where you can unfold the full palette of your knowledge including having an impact and being able to influence how we work on a global scale, this is the right job for you. In Ferring you will join a successful, global market leader and work with a broad and exciting product portfolio – and you will do it together with highly skilled colleagues.

 

Audit program development, planning, audit execution, training, advisory
As GVP Specialist and Auditor your overall focus is the safety of patients all over the world. You will become a valuable GVP expert in the Global QA organization meaning you will have ample opportunities to influence our way forward while making an important and tangible difference across the global organization.

 

Your primary tasks will be to:

 

  • Support the preparation of the Global QA program for pharmacovigilance activities
  • Support the preparation of the risk assessment and global audit plan for GVP related audits
  • Plan, execute and report global GVP related audits
  • Contribute to follow up on GVP audit observations and trending of observations and CAPAs
  • Serve as GVP expert supporting colleagues across Ferring globally
  • Support the preparation of training programs and train local and global stakeholders in GVP aspects
  • Participate in preparation for and during Regulatory Inspections

 

You will spend time travelling to perform audits at Ferring Sites, Pharmacovigilance partners and suppliers. However, due to the use of remote methods for auditing there are possibilities for influencing the amount of travelling. Some of your travels will also be to share knowledge, attend trainings and conferences, optimize best practices and build good relations to colleagues in cross-functional GVP compliance meetings.

5+ years’ experience within GVP processes
We are looking for a profile with knowledge, experience and drive to take on a role as outgoing expert and enabler for the business. You must bring at least 5+ years’ experience from working with GVP processes either from a business perspective or QA. If you already are an auditor by training e it is a plus but not a prerequisite for applying.

As you will be working cross-organizationally you will need all of your ability to collaborate and create sustainable relationships – across cultural, professional and geographical borders. This requires very good communication skills including the ability to tailor your messaging to your audience (in fluent English, written and spoken). Additionally, you will need a structured work approach and the ability to keep track of multiple parallel assignments.

 

Your new team and workplace
You will join a new team of approx. 7 competent and dedicated colleagues being responsible for the overall quality assurance and audit of Ferring’s Global R&D and Pharmacovigilance activities. Your new colleagues are experienced Quality Experts like yourself and we primary cover GVP and GCP regulated areas. The working atmosphere is characterized by respect, helpfulness and a shared passion for improving life for our patients. Your new workplace is at the spectacular and state-of-the-art new domicile “SoundPort”, an architectural landmark on the coast next to “Den Blå Planet”, minutes from Copenhagen Airport.

 

Additional information

For additional information, please contact Head of Global Clinical Quality Caroline Sandström on +452878 7211.

Your application and CV in English should be sent as soon as possible and no later than 4 November 2022.

Please note that all applications must be send through our career page:
https://ferring.wd3.myworkdayjobs.com/en-US/Ferring/job/Ferring-Denmark…

Please note that we review applications on an on-going basis and close the process when we find the right match – the sooner you apply the better are your chances.

 

Ferring Pharmaceuticals is a leader in reproductive medicine and maternal health, and in specialty areas within gastroenterology and urology. At Ferring International PharmaScience Center (IPC) in Copenhagen we are nearly 600 people, primarily scientists and specialists breaking new ground to help people live better lives all around the globe. We focus our R&D efforts on peptide-based drugs and biotechnology derived medicines.

 

As a privately-owned company we benefit from the privilege to think and work with a long-term horizon. You will experience the same freedom in your search for new solutions. Your desire to innovate and explore will contribute to fulfilling our ambition of becoming the world’s leading company within reproductive medicine and maternal health. If you need help, you will find it. If you want challenges, they are right in front of you. If you are looking for freedom to find your own way, you are trusted to do so. If you want to make a mark in the world for the better, you feel just like the rest of us. Read more at ferring.com

Job details
Education field:
Work experience:
Work experience is required
Duration of work experience:
More than 5 years
Language skills:
  • English
  • Fluent
Number of positions:
1
Date of expiry:
Link for more information:
About company

The Danish job market is booming and many sectors are facing skills shortages. Therefore, there are many sectors with good job opportunities one of them is Life Science. The Danish life sciences industry, comprising almost 1.500 life sciences companies and approximately 47.300 employees, contribute considerably to both R&D, economic progress and employment in Denmark. Subsidiaries of most of the major international life sciences companies are already present in Denmark, employing over one fourth of all employees in the Danish life sciences industry. In Denmark, there is a long-standing tradition for efficient public-private partnerships in areas such as development and testing… Read more