Senior Regulatory Professional – Regulatory Clinical, Non-Clinical & Operations

Do you have an interest in Regulatory Affairs and experience in working with regulatory submissions? Do you want to be part of a team who are involved in both development activities as well as lifecycle activities and who support each other to reach the goals in a busy everyday life? Do you have an eye for detail but are also capable of seeing the bigger picture? Then you are the right person to apply for our open position!

The position
One of ALK’s important strategic priorities are to build a portfolio in anaphylaxis, and for our adrenaline business we are looking for a regulatory colleague to manage various regulatory activities. You will join the team Injectables, Drops, Diagnostics and Devices in the department Regulatory Clinical, Non-clinical & Operations (RCNO) which is part of Global Regulatory Affairs, Safety & Pharmacovigilance. You will be based in our Head Office in Hørsholm. The working environment is informal and flexible.

The role is of strategic importance, and having experience in centralized EU regulatory procedures is an advantage. You have a can-do attitude to steer a submission team with the main goal of submitting the right documentation at the right time.

Your responsibilities will depend on your experience. Your daily tasks will cover preparation of regulatory documentation and handling of the submissions to authorities. As there are several parallel activities and deadlines to manage your good planning skills will come into play.

In this role you will among others:

• Be responsible for reviewing, compiling and maintaining regulatory clinical and non-clinical documentation for submission of applications for new marketing authorisations for a nasal adrenaline product.
• Be responsible for preparation and submission of life cycle management applications.
• Have cross-functional and external cooperation related to new Marketing Authorisations and product life cycle activities.
• Be responsible for having an overview of submitted and approved clinical and labelling documentation globally.
• Update and maintain Product Information and Printed Packaging Material and ensure timely implementation.
• Handle educational materials for adrenaline drug/device combination products.
• Take part in discussions on regulatory strategies.
• Provide regulatory guidance for various cross-functional areas (e.g. clinical development, commercial operations, safety & pharmacovigilance).

Your qualifications
You have a Master of Science within a relevant field, e.g., in pharmacy, engineering preferably combined with working experience within regulatory submissions. You thrive in scientific discussions with the goal of clarifying needs and identifying solutions, and you enjoy preparing clear and logically organised written material on complex scientific matters.

Moreover, we expect:

• Basic knowledge from the pharmaceutical industry including GxP.
• Openness towards other departments and external stakeholders.
• Service-minded and a profound team-player.
• Excellent communication skills and good English skills, both in writing and orally.
• Taking on responsibility for having the job done and being well-structured and organized.
• Result-oriented and able to keep the perspective in times of increased activity.
• A great sense of humour.

Become a part of ALK
We provide an attractive working environment for individuals looking for both personal and professional development. ALK is a global pharmaceutical company specialized in allergy immunotherapy. We are driven by a high level of professionalism, integrity, an openminded approach and contributing to an inspiring and fun working environment together with our colleagues. You will be part of an engaged and informal team who values skill and knowledge creation.

Our offices in Denmark offer a green view of the DTU Science Park in Hørsholm. We believe that physical presence enforces strong teamwork and collaboration and creates success, so it is important that you enjoy coming to work in our office in Hørsholm but we also provide a degree of flexibility to work from home.

Apply
Apply by attaching your CV and a short letter of motivation, no later than 4 April 2025.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We evaluate applications and call for interviews on an ongoing basis, so don't wait to apply! We reserve the right to take down the advert when we have found the right candidate. Do you want to learn more about our company, we encourage you to visit us at [xxxxx] For further information regarding the position please contact Director, Lotte Bruun Christiansen on +[xxxxx].

We are looking forward to hearing from you!