About this role
Location: Høje-Taastrup Are you an experienced analytical scientist, who is thrilled about the idea of bringing new products to market? Join us on an exciting journey as we pursue an ambitious strategy for synthetic chemical API Ingredients If this sounds like you, we look forward to welcoming you to our department for External Analysis in Synthetic API and Contract manufacturing. Submit your application today!
The Position As an Analytical Scientist your primary role is providing scientific and GMP expertise to CMOs. Our department is responsible for ensuring that a robust and efficient analytical program is implemented at the CMO’s and maintained throughout the life-cycle. Moreover we are also taking lead on regulatory submissions.
Your key responsibilities will include: Scientific and/or procedural support and expertise to CMOs or to other stakeholders Supporting analytical activities (incl. submission) from post phase 3 clinical studies throughout commercial life cycle Handling technical transferring and implementing analytical methods to/from collaborative partners Authoring and editing SOPs, reviewing protocols, reports, tech transfer plans, and other documentation Build and optimize internal processes and SOP’s to support our daily work As we are a developing area, you must be comfortable in situations where the path is not clear and not afraid of challenging the status quo. You will be part of a team of subject matter experts, fostering an open, positive, and collaborative atmosphere for discussing ideas, problems, and solutions. Given that many CMOs are internationally based, the position may involve some travel, and meetings outside of normal working hours can occur.Travel is expected to be less than 14 days a year.
Qualifications To succeed in this role, you: Hold a minimum of a Master’s degree in Pharmacy, Chemistry, Biochemistry, Chemical Engineering, or other similar scientific disciplines Have a minimum of 3 years of experience in a similar position, ideally within the pharmaceutical sector You have hands-on experience working in a GMP regulated environment, e.g. QC laboratory Possess strong knowledge within GMP, ICH guidelines, and pharmaceutical regulatory requirements Working with deviations, change request, out of specifications is part of your experience Showcase full professional proficiency in both spoken and written English Knowledge of late phase (phase 3 and ongoing) pharmaceutical development and validation combined with previous experience working with chemical synthesis (e.g. small molecules or peptides) is an advantage. Having experience or interest in exploring and implementing AI tools within a regulated environment is also seen as an advantage.
As a person, you thrive on a high level of flexibility and adaptation, enabling you to excel in a role where the quality of your work is paramount. You have “a firm hand” when it comes to science and possess good skills at communicating with all types of stakeholders both verbally and in writing, and you are motivated by the opportunity to expand your network within our field. About the Department External Analysis & QC is a department currently with teams based in USA and Denmark.
We have a growing pipeline, many of which are based on new technology platforms coming through internal development projects or acquisitions. You will join a diverse team of Analytical Project Managers, Senior Analytical Professionals & Analytical Professionals. ET is well-known for having a pioneering spirit as well as a curious and daring approach and we play a key role in developing and producing future treatments for millions of patients around the world.
What we offer At Novo Nordisk, you’ll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage. Salary: For this role, the Annual Base Salary ranges from .............. to ................
DKK, corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience. Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area, and relevant market benchmarks.
Learn more about our Reward Philosophy her e . Deadline: 23 of August. Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare.
We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.