Product Specialist - Oral Solid Dosage Forms

Are you passionate about providing expert product knowledge and setting the direction for future tablet production to the benefit of our patients? Do you have intense knowledge and interest in the stability of products in oral solid dosage forms as well as solid experience in working with requirements from Health Authorities to ensure a compliant product? Are you a specialist within products in Oral Solid Dosage Forms, if so, this is a unique job opportunity for you, apply now!

The Position

As product specialist you will be a key player in ensuring product quality across our marketed drug products. Keeping the helicopter perspective across the different drug products with APIs (Active Pharmaceutical Ingredients) in the form of e.g. proteins, synthetic peptides and small molecules is key to your role. You will have a wide variety of collaborative partners across the entire ET organisation thus supporting our 3 manufacturing sites and QC labs in Måløv DK, Durham US and Athlone IE.

You will also be responsible for

Qualifications

Our ideal candidate has:

The complexity of the role requires you to have excellent skills within stakeholder management and as a person, you have a high-quality mindset and meet your deadlines. You need to have extensive business understanding across the SVP area to ensure optimal use of resource, cost, environmental impact as well as keeping the quality standards.

With your structured approach to your tasks, you maintain an overview - even in a changing environment where priorities can change quickly. Personal drive, energy and a positive attitude are essential. We continuously look for opportunities to introduce modern technology into our existing facilities, so a keen interest in digitalization and automation will be an advantage.

About the Department

Emerging Technologies (ET) is a newly established area in Novo Nordisk. We have a growing pipeline of new products, many of which are based on emerging technology platforms coming into Product Supply via internal development projects and externally acquired assets. ET are 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. The area is anchored in Product Supply, Quality & IT, which globally employ approx. 25,000 of Novo Nordisk’s 55,000 employees.

You will be joining the area Drug Product Manufacturing Development & Quality Control (DP MDev & QC), which has process and product responsibility for existing and future oral drug products post-launch, as well as performing all analyses on products after method transfer. We work across the ET organization to improve productivity of our production and analytical processes. You’ll be joining the Project Office of DP MDev&QC that anchors top specialists and strategic project managers within tablet product, production and supporting processes.