Novo Nordisk

Due Diligence & Integration Quality Director

Fuldtid

Permanent

Gladsaxe

SE PÅ KORT

ID: 2600934

Indrykket for 13 dage siden

Are you an expert in GMP, GCP, GLP, and health authority regulations? Are you ready to make a significant impact on the quality of our products and services? We are seeking a dedicated professional to join our NNQ Due Diligence & Integration team at Novo Nordisk. If you are passionate about ensuring compliance and driving improvements, read on and apply today for a life-changing career.

The position
As a Due Diligence & Integration Quality Director at NovoNordisk, you will play a critical role in ensuring compliance with health authority regulations and requirements all the way from the Due Diligence activities and until the new project is fully handed over to NovoNordisk. You will be a significant contributor to the development and execution of the Q functional integration strategies.
Your responsibilities include supporting and leading pre-due diligence and due diligence projects, providing expertise in GMP, GCP, and GLP. You will actively be building up and maintaining a network related to Quality topics on Due Diligence and Integration, ensuring optimal integration of acquired assets, technology, and companies into NovoNordisk QMS.

Furthermore, you will:

Act as NNQ expert within Due Diligence and Integration in Quality across the EVP areas; Product Supply, Corporate Quality, IT, Corporate Development and Business Development ensuring compliance with health authority requirements.

Lead evaluation of all Quality aspects of new asset opportunities and potential new companies, contributing to the development of the Q functional integration strategy.

Maintain state-of-the-art competences and know-how within Due Diligence and Integration in Quality, actively capturing and sharing novel substance matter.

Anticipate internal and/or external business challenges and recommend process, product, or service improvements within Due Diligence and Integration in Quality.

Advise on deals, potential risks, and impact from a quality perspective on behalf of the global quality organisation.

Train and mentor others.

Qualifications
To be successful in this role, we are looking for a candidate with the following qualifications:

An academic degree, e.g., B.Sc. in Engineering.

Extensive and relevant experience in the pharmaceutical industry.

Expertise in GMP, GCP, GLP, and/or device regulations (MD/DCC).

Experience in M&A in Pharma, including Due Diligence and Integration.

Have a profound business understanding.

Good English skills and experienced presenter.

As a person, you operate with an exceptional degree of independence, adding value to every deal phase by providing crucial professional insights and shaping potential integration strategies from a quality perspective. You excel in driving changes, fostering innovation, and embracing new ways of working. Your ability to engage stakeholders, collaborate across boundaries, and lead discussions to mutual conclusions is fundamental to your approach. Additionally, your talent for improving work processes and documentation structures to enhance efficiency and compliance sets you apart in complex environments.

About the department
The NNQ Due Diligence & Integration team is responsible for ensuring the quality of our products and services throughout the due diligence and integration process. We work closely with various EVP areas and stakeholders to evaluate new asset opportunities, develop integration strategies, and drive improvements in quality. Our team is dedicated to maintaining compliance with health authority requirements and driving innovation in our ways of working.

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