Analytical Support Professional

Do you like to improve and trouble shoot biochemical analytical methods for pharmaceuticals? Do you like to work with data, and do you enjoy using statistical tools such as SAS-JMP? Do you like to take responsibility, and do you enjoy a collaborative environment?

We are looking for an Analytical Support Professional to join our QC Analytics organization. In this role, you will be troubleshooting analytical challenges, driving continuous improvement, and helping transform complex technical issues into practical and user-friendly solutions. You will work across functions, and stakeholders to ensure analytical processes remain robust, compliant, and efficient while continuously improving the way we work.

The position
QC Support is a team within QC consisting of 10 academics and 4 technicians. As a QC Support professional, you will have a varied role in which you will take part in optimizing methods and processes within our area of responsibility. In QC Support, we are responsible for the critical reagents including in-house references for immunochemical methods such as TAPE, RID, CIE, SDS, and HPLC. This includes qualification and implementation of critical reagents and ensuring that any change in reagent does not affect analytical performance. In addition, we are responsible for stability monitoring of drug substance (DS) and in-house references (IHRP), preparation of Justifications of Specifications for IHRP and DS, as well as validation, verification, and comparability of methods and reagents. Finally, we support our regulatory department with source documentation for regulatory submissions.

We have close collaboration with the other teams in QC and with Product Leads, CMC analytical development, Global Regulatory Affairs and Production and QC sites in and outside of Denmark.

Your primary tasks will be:

• Drive life cycle management of immunochemical methods including troubleshooting, optimization, development, and validation.
• Prepare and update Justifications of Specifications, including statistical calculation of specification limits.
• Be responsible for developing user friendly statistical methods for QC, and establish statistical foundations e.g. for the justification of acceptance criteria.
• Act as a problem solver for complex laboratory and data-related challenges.
• Translate technical complexity into clear recommendations and practical solutions.
• Participate in the routine tasks within the team, including reporting on stability studies, implementation of new lots of critical reagents etc.

Your profile
We expect that you:

• Have a relevant academic background, e.g. cand.scient or cand.pharm, with a minimum of 5 years of relevant experience.
• Have experience with validation of biochemical analytical methods and knowledge of analytical method development.
• Have in-depth knowledge and understanding of immunochemistry within the pharmaceutical industry and are up-to date with the guidelines.
• Have experience in submission of new analytical methods to authorities.
• Have flair for statistics and solid experience with statistical software such as SAS-JMP.
• Can provide support and create solutions within the frames of GMP.
• Can make complex issues understandable and actionable.
• Preferably experience working with laboratory systems, automation, digitalization, or data analytics.
• Possess strong collaboration skills.
• Takes pride in reaching agreed deadlines and lead times. 
• Strive to be the best colleague and always have a focus on team excellence.

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 specialised in allergy immunotherapy. We are driven by a high level of professionalism, integrity, an open-minded 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. The result of your efforts will be significant throughout the organisation, and you will be able to actively influence and challenge the status quo.

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 at our site with a degree of flexibility to also work from home.

Apply
Apply by attaching your CV and a short letter of motivation, no later than 6 September 2026.

We commit to an inclusive recruitment process and equal opportunity for all our job applicants. Hence, we prefer that you do not add images in your application documents. 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 www.alk.net. For further information regarding the position please contact Senior QC Support Manager, Rikke Stavnsbjerg on +45 41959025.

We are looking forward to hearing from you!