Novo Nordisk

QA Professional/QP Delegate - 2 years maternity cover

Fuldtid

Tidsbegrænset

Novo Nordisk Park 1, 2760 Måløv, Danmark

SE PÅ KORT

ID: 2715751

Indrykket for 4 dage siden

Are you a pharmacist or do you have a similar education that enables you to function as a Qualified Person Delegate in the pharmaceutical production? We are seeking qualified professional to join our dedicated and dynamic QA team in Måløv . If you are ready to contribute to something impactful and make a difference for many, we invite you to apply and be a part of our team.

The position
As a QA Professional/QP Delegate, you will be part of the process of launching the next generation of RYBELSUS® tablets. In collaboration with production, you will ensure timely production, review and release of our new products. You will be responsible for continuously optimizing our workflows and ensuring that our processes are ready for the future.
Your primary tasks will be:

Batch review, with a focus on reviewing batch documentation for both blend and tablet batches to ensure correct production processes, guaranteeing both quality and compliance

Ensure daily review and release of a specified number of batches to prevent QA from becoming an impediment for delivery, while offering support and professional collaboration as needed

Collaborating with colleagues and production supporters in an open-plan office, fostering dynamic and energetic collaboration, and maintaining pace with production requirements to ensure on-time medication delivery

Qualifications
To be successful in this position, we expect you to have:

As required by the Danish Medicines Agency's for a QP or QP Delegate, you must have a university degree of at least 4 years’ duration in pharmacy, medicine, veterinary medicine, chemistry, pharmaceutical chemistry and technology or biology. This is a non-negotiable requirement, as you will eventually be responsible for releasing our products

Preferably experience in either tablet production or QA in the pharmaceutical industry

Thorough and detail-oriented approach to documentation, ensuring quality and compliance without compromising patient safety

Proficiency in LEAN methodologies and digitization, actively contributing to process efficiency and optimization efforts, working closely with production to enhance process flow

Flency in Danish language

On a personal level, you are proactive and take the lead in problem-solving, both in daily tasks and when coordinating efforts with colleagues. You should be adept at meeting deadlines and committed to ensuring that our patients receive their medication in optimal quality and on schedule. Additionally, we value a curious mindset that challenges the status quo, as our team is dedicated to continuous optimization and discovering smarter approaches to our work.

About the Department
The department consists of approximately 50 colleagues, divided into 4 teams who handle QA tasks related to tablet production. The entire area we support is rapidly evolving, and production volume is increasing significantly year after year. You will be part of a team of about 9 people, where collaboration, coordination, and effective communication are key to success. We are QA for tablet production in Måløv. This means that, together with production and various support units, we are responsible for maintaining our license to operate and ensure a sufficient level of compliance and quality. We have a strong team spirit and we prioritize having fun while at work. We believe in creating a work-life balance with flexibility and understanding of individual needs, but at the same time, the whole team is also ready if situations arise that occasionally require extra effort.

Husk at skrive i din ansøgning, at du så jobbet hos Ofir