Analytical academics with experience and motivation for Quality Control - Oral Finished...

• Quality
• Måløv

Do you want to join us on a journey where you, as a true pioneer, will break new land? Then apply now for a position in our Oral Finished Products QC (OFP QC) department in Måløv, as we are expanding and looking for dedicated, professional and enthusiastic new colleagues to join our team. You can look forward to a job where you will set direction for the future work in a recently established department and where your effort will be of invaluable importance for the lives of people living with diabetes.

About the department

In OFP we are approximately 400 dedicated employees in Måløv and the area is still growing. For the future we have many ambitions - together we will succeed and still strive being at the forefront of the development of technology, systems and processes etc.

Oral Finished Products Quality Control (OFP QC) employs approximately 70 highly skilled and motivated employees in five teams. The department delivers analytical support to oral protein products from clinical phase 3 to marked product. OFP QC support the production of oral finished products and ensure analytical support to manufacturing development. We are working with standardisation and optimisation of our procedures to ensure robust QC processes.

In OFP we make a huge effort for you as a new employee to be off to a good start. During the first few days you will spend some time with other new employees, where you will go through an exciting introducing plan together. The department manager will welcome you, and a colleague will act as a mentor and go through your individual training plan. We know how important it is, and we are looking forward to meeting you.

The position

As an analytical scientist in OFP QC, you will ensure valid analytical results by approval of analytical test results and provide support to HPLC/UPLC based methods e.g. assay, dissolution, impurity, content uniformity and other methods such as Karl Fischer, UV, disintegration and particle size distribution. Maintenance, optimisation and validation of analytical methods will also be a part of the job, as well as leading projects on relevant issues when they arise. You will be working to continuously ensure optimal performance of the analyses and apply LEAN principles to trouble-shoot and improve our working procedures. You will communicate and coordinate with stakeholders internally as well as externally within various subject areas.

Qualifications

You have a background as a pharmacist, cand. scient. or similar, and you have a solid background from laboratory work in a GMP regulated environment. You have experience with approval of analytical test results, validation and standardisation of analyses. Competences within tasks such as method validation, preparing, updating and reviewing instructions, Non-Conformity reports and Change Requests will be considered as a plus.

As a person you thrive on a high level of flexibility – and with your ability to adapt you will enjoy a position where two days are not the same. You work in a structured manner with a non-compromised focus on quality. At the same time, you appreciate a good working environment where you with your dedication, good personality and initiative contribute actively to solutions to various types of challenges. Finally, you contribute to a healthy working climate and the continuous improvement of processes.

Contact
For further information please contact Maria Berg on [email protected].

Deadline

March 20, 2020

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.