Product Specialist - Oral Solid Dosage Forms (Denmark, Måløv)

Jobbeskrivelse
Placering
Måløv, Denmark

Jobkategori
Manufacturing

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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

• Supporting our Drug Product Project Managers and Life Cycle Management department upon critical product related cases and ensuring our drug product lives up to its specification.
• Providing specialist product knowledge upon implementing process optimisations and new technology.
• Identifying and taking initiatives to build product knowledge across the entire ET organisation e.g. by initiating projects to be run by master students.
• Providing product specialist knowledge in due diligence projects upon acquiring potential new assets, production processes and products.

Qualifications
Our ideal candidate has:

• Relevant academic background such as pharmacist, chemist, engineer or similar scientific/technical education.
• Solid experience from a GMP-regulated production environment.
• + 10 years of experience in product stability and product specifications, preferably within solid dosage forms.
• Keen interest in supporting and mentoring junior employees.
• English communication skills in writing and spoken is essential.

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.

Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.

Contact
For further information, please contact Snr. Manager Mie Houlberg Danielsen; [email protected]

Deadline
May 5,2024.

Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified.

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 in your CV.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.