Jobdetaljer

Jobtype

Fuldtid

Permanent

Komplet jobbeskrivelse

Descripción del puesto:

Are you passionate about optimising tablet manufacturing processes and investigating the raw materials’ impact on product quality? Do you want to be part of a dynamic department who among other exciting tasks holds the responsibility of bringing new oral products for the treatment of diabetes and obesity from development to market readiness? Then this might be the right position for you!

The Position

In this job you will participate in the transfer of new products from R&D to the production sites in both DK and US. You will also be responsible for continuous optimization of already approved products – also called Life Cycle Management (LCM). Sometimes with special focus on the raw material characteristics on the tablet production performances.

As we expand our product portfolio and our production sites, we are also expanding our use of raw material and raw material suppliers. We expect you to participate in the ongoing implementation of new variations of our raw materials.

You will contribute to:

  • Life Cycle Management of tablet production

  • The implementation of new raw material suppliers, including the responsibility of testing the raw material in full-scale production equipment

  • Challenging test methods of powder materials and contributing to developing these to improve tablet production processes.

  • Project Management by leading projects and tasks across the organisation.

To succeed with all this, you will need to combine your process and drug product understanding with a good quality mindset for the finished product. You will also have to build relations with your colleagues in the production, Quality Control, Quality Assurance and Regulatory Affairs areas.

When necessary you will be driving root cause analysis and trouble-shooting sessions in cooperation with the production and analytical departments.

Qualifications

  • You hold a master’s degree and/or a PhD in science within Pharmacy, Chemistry, Engineering, or a similar field.

  • You have extensive and documented experience from within the field of CMC or manufacture, e.g. product development, support, transfer, or process validation.

  • You have experience within oral formulation and tablet production

  • You collect and evaluate production process data and understand the impact on tablet production

  • You possess good communication skills in both oral and written English and preferable also Danish.

  • You possess a project management toolbox to coordinate tasks between sites.

About the department

Oral Finished Products (OFP) MDev Support and stability employs approximately 50 highly skilled and motivated employees with the missions to bring products from late development to market production, optimize the processes and products, support the production sites, document the stability for the products and build up the documentation for authorities for new products and for marketed products.

The department consist of 3 teams: Drug Product & Stability, Support for marked products and Support for New Product Entry products.

What we do is an important part of Novo Nordisk, and as an agile department, we solve exciting and challenging tasks every day.

Working at Novo Nordisk

At Novo Nordisk, we don’t wait for change. We drive it. We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today, is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.

Contact

For further information, please contact Jacob Holst Madsen at +xx xxxxxxx0.

Deadline 1 August 2022

You do not need to attach a cover letter to your application, but please include a few lines about your motivation for applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo onto your CV. You can apply in either Danish or English.

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

Skriv i din ansøgning, at du fandt jobbet på ofir.dk

Indrykket: 5 aug 2022

Indrykket: 5 aug 2022

ID: 331254136

Adresse

iAgora Europa

Fuldtid

Permanent

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