Specialist for CMC Injectable Drug Product Development

Specialist 
CMC Product & Process Development
CMC Injectable Drug Product Development
Måløv, Denmark.

Transform scientific insights into tomorrow’s therapies

As our new Specialist, you will help influence Novo Nordisk’s promising pipeline and contribute to the development of tomorrow’s drug products. This role involves driving both early- and late‑stage development projects, supported by deep scientific expertise within formulation development of peptides, proteins, antibodies, or minibinders.

If you are driven by scientific curiosity, technical leadership, and the opportunity to push formulation innovation forward, this role offers a strong platform for impact and growth within Chemistry, Manufacturing and Control (CMC) Injectable Drug Product Development. Apply today and lead with scientific impact.

Your new role 

As our new Specialist, you will take scientific ownership of one drug modality in the pipeline, bridging insights across projects and anticipating future formulation challenges.

As part of a dynamic CMC environment in Måløv, you will collaborate closely with experts in Global Research, Regulatory Affairs, Quality Assurance, and Analytical Development to translate molecular innovation into clinical‑ready drug products and strengthening our way of bridging knowledge between projects and foresee future formulation challenges across the portfolio. 

You will play a pivotal role in leading product and process development to secure optimal pharmaceutical characteristics and stability. Furthermore, you will:

• Lead formulation and small-scale process development activities for one of our drug modalities from early to late phase development (Ph I–III)
• Develop strategies to design, execute, and interpret formulation and stability studies, and prepare clear study reports for internal use, patent filings, and regulatory submissions
• Drive innovation initiatives and propose new formulation strategies or technologies
• Mentor and guide colleagues and lab staff on experimental approaches and problem solving
• Collaborating with a wide variety of internal stakeholders in the Novo Nordisk value chain.

This role offers growth toward senior scientific leadership, technical authority roles, or project lead responsibilities.

Your skills and qualifications

To succeed in this role, you hold a PhD or Master’s degree within Pharmaceutical Sciences, Engineering or another relevant natural science field. You also bring:

• A minimum 6+ years of working experience within one of the above-mentioned molecular drug modalities.
• In-depth knowledge of working within R&D or drug product development across all phases of development (Ph I-III)
• Demonstrate an innovative, proactive and engaging mindset to move projects forward and inspire teammates.
• Ability to work independently and with others across a complex stakeholder environment.
• Communicate fluently in written and spoken English.

On a personal level, you thrive in a collaborative scientific environment while confidently driving your own area of expertise. You take the lead when needed and are comfortable influencing colleagues and stakeholders through evidence‑based reasoning. You enjoy a dynamic setting where priorities and projects evolve, and you adapt quickly to new data and challenges. You communicate complex scientific insights clearly to diverse audiences and inspire others to engage with and act on your ideas.

Your new area

Chemistry, Manufacturing and Control (CMC) Injectable Drug Product Development is part of CMC Product & Process Development. We develop formulations and production processes for injectable biopharmaceutical products. We are approximately 100 employees organised into six teams, all located in Måløv. We manage projects from early development (Phase 1–2) through late‑stage and process validation (Phase 3–PV), covering GLP‑1 products, insulins, monoclonal antibodies and minibinders. 

In our department we put in an effort for a culture where we care for another and a culture where you have a possibility to take initiatives and drive projects forward and grow professionally. 

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.

More information

Due to the volume of applications, we do not offer pre-interview calls. However, if there are practical challenges related to the application process, please contact Senior Talent Acquisition Partner Helle Krogsgaard at HKGS@novonordisk.com

Deadline

22 March 2026.

While not mandatory, we strongly encourage the submission of a cover letter, explaining why you are the ideal candidate to join us in CMC Injectable Drug Product Development. Please refrain from adding a photo to your CV to ensure fair and efficient processing.

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.