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QP delegate for a fast-growing tablet production

Category:  Quality
Location: 

Måløv, Capital Region of Denmark, DK

   

Are you an experienced QA Professional or QPd who is eager to set direction and to ensure compliance together with our stakeholders in close collaboration? Do you thrive in a constant changing environment?  

 

Then you can be part a team with responsibility for quality assurance for production and packaging of tablets in Oral Finished Product QA. We are also involved in the transfer of new tablet products from development to marked production. You will have influence and set directions in setting the right level of compliance, optimizing our processes and establish new processes in collaboration with stakeholders.    

 

We can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. In OFP QA our department consist of colleagues based in both Måløv and Durham US.

 

The job

You will be trained to become a QP delegate and you will have the overview of the processes within production of oral medicinal products. In QA we have the quality oversight and are physically present in the production to observe performed processes and help solve issues in real time.

You will perform review of batch documentation as well as review of batch and process related documentation from our stakeholders including deviations, change requests, SOPs etc. Our core task is to ensure that we get products out to our patients at the right quality and in a timely manner.

You will set directions and deliver results which have a significant impact within the context of our business. Your focus will be assuring that the documentation related to the manufacture of drug product for the market is compliant with internal and external requirements. You have a risk-based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.

We can offer an exciting and challenging position, where you become part of a competent team that acts as sparring partners and problem solvers in quality issues for the production. You will drive optimizations and projects to continue improve processes and implementing new tablets.

 

Qualifications

You hold a MSc in Pharmacy, Microbiology, Veterinary medicine or similar. You have 4+ years of experience with GMP and quality assurance - preferably within batch release/status assignment.

We are looking for an open-minded person with high level of energy, an outgoing attitude and have very strong communication and collaboration skills. We are looking for a person with an innovative mind, who is able to see new and optimized solutions.

You have a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production and hence can navigate without adding complexity.

You are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks. You thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders.

As we operate both in a national and an international environment, you must speak and write Danish and English fluently.

 

About the department

Oral Finished Products QA is a department which employ approximately 50 skilled and motivated colleagues. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets for the market. We are proud to work in a fast-growing and ambitious part of Novo Nordisk.

 

Contact

For further information, please contact Associate Manager Linea Frenk Alsing +45 3075 6596.

We will conduct interviews continually.

 

Deadline

Deadline to apply for this position is February 6th 2022.

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.