Corporate Vice President, Head of Quality for Research and Development
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Are you passionate about quality and leading others across Research and Development to raise the quality ambition for Novo Nordisk? Then this could be the opportunity for you! We are seeking an ambitious Corporate Vice President as head of Research and Development Quality.
About the person
The person we are seeking will be ambitious on behalf of Novo Nordisk and our Research and Development organisations to ensure robustness, elevate compliance and drive simplicity for our quality management systems across GxP processes. The person should be comfortable with and possess extensive experience in building strategy, clearly communicating a vision, adapting to change, being empowered to act and lead others within their area and across a large R&D organisation.
About the position
The Corporate Vice President (CVP) is responsible for setting the strategic direction, and for defining, organising, and leading the quality assurance activities covering Research and Development in Novo Nordisk. The position leads an organisation which sets the ambition for quality and compliance activities of approximately 7000 colleagues working closely with Process Owners for GxP regulated processes.
The CVP and R&D quality team area are working to execute on the recently updated strategic priorities within Novo Nordisk covering optimized clinical trial processes, new device platforms, new cloud based GxP process delivery solutions, Software as Medical Device (SaMD), as well as external partnerships. The position is responsible for quality assurance leadership impacting ICH, GxP, MDR and ISO requirements as well as Novo Nordisk internal requirements. The right candidate has experience in ensuring inspection readiness, leading, and supervising activities for GCP inspections at an executive level and ensures inspection or audit findings are communicated and actions taken. The candidate will also lead the QA function’s role in business development and integration as Novo Nordisk continues to enhance our development pipeline.
Across R&D, we have a strong focus on adapting processes and the way we work, and as the future leader of this function, you will be playing a key role in driving new strategic and improvement initiatives. Through this, you will have excellent opportunities to drive impact across the R&D value chain by leading and developing an industry-leading Quality function. You will be comfortable working with all levels of seniority and diverse stakeholders across Research & Development and Quality. You will report to the Senior Vice President of Submissions and Life Cycle Management in Development with a dotted line to the Senior Vice President of Novo Nordisk Quality, where you will also be part of the Novo Nordisk Quality Management team.
Qualifications
You have a relevant educational background, e.g., MD, PhD or master’s degree in pharmacy, natural sciences or engineering and extensive experience within drug and biologic development as well as: Substantial business understanding and experience from positions within the R&D value chain Demonstrated ability to drive the establishment of lean and fit for purpose process landscapes in regulated environments – prior QA leadership experience within/impacting pharmaceutical/biotech Research and Development is a requirement. Extensive experience of GCP regulated processes is a distinct advantage. Strong focus on continuous improvements to enable a highly productive quality organisation Proven experience with change management Strong People management track record both through their own team as well as ability to lead through the matrix We are looking for a candidate who sets direction, builds, and leads a strong team able to impact our development portfolio as QA partners and QA responsible. With increasingly new external requirements coming forward there is a need to address these proactively and prepare the organisation from QA and into the line perspective. We expect that you are curious to learn, change prepared and have great communication and collaborative skills to ensure enhanced collaboration with key stakeholders across organisational borders.
About the area
R&D Quality is a growing, dynamic area with responsibility for assuring quality across both the Research and Early Development and the Development organisation. We are over 130 dedicated colleagues divided into 4 different areas, R&D Quality Operations, Clinical Quality, Global Safety Regulatory Affairs & IT Quality and Device and Delivery Solutions Quality. You will be part of a high performing culture with focus on quality, patient safety, cross-functional collaboration and both personal growth and professional development. We are passionate about reaching ambitious goals as a team, we are curious and courageous, always striving for simplicity and we believe in developing people through trust and empowerment.
Contact
To learn more about the position, well qualified candidates are welcome to contact Robin Evers on +45 30795206 between 17th- 21st July. No agency calls please.
Deadline for applications
4 August 2023 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.
About the person
The person we are seeking will be ambitious on behalf of Novo Nordisk and our Research and Development organisations to ensure robustness, elevate compliance and drive simplicity for our quality management systems across GxP processes. The person should be comfortable with and possess extensive experience in building strategy, clearly communicating a vision, adapting to change, being empowered to act and lead others within their area and across a large R&D organisation.
About the position
The Corporate Vice President (CVP) is responsible for setting the strategic direction, and for defining, organising, and leading the quality assurance activities covering Research and Development in Novo Nordisk. The position leads an organisation which sets the ambition for quality and compliance activities of approximately 7000 colleagues working closely with Process Owners for GxP regulated processes.
The CVP and R&D quality team area are working to execute on the recently updated strategic priorities within Novo Nordisk covering optimized clinical trial processes, new device platforms, new cloud based GxP process delivery solutions, Software as Medical Device (SaMD), as well as external partnerships. The position is responsible for quality assurance leadership impacting ICH, GxP, MDR and ISO requirements as well as Novo Nordisk internal requirements. The right candidate has experience in ensuring inspection readiness, leading, and supervising activities for GCP inspections at an executive level and ensures inspection or audit findings are communicated and actions taken. The candidate will also lead the QA function’s role in business development and integration as Novo Nordisk continues to enhance our development pipeline.
Across R&D, we have a strong focus on adapting processes and the way we work, and as the future leader of this function, you will be playing a key role in driving new strategic and improvement initiatives. Through this, you will have excellent opportunities to drive impact across the R&D value chain by leading and developing an industry-leading Quality function. You will be comfortable working with all levels of seniority and diverse stakeholders across Research & Development and Quality. You will report to the Senior Vice President of Submissions and Life Cycle Management in Development with a dotted line to the Senior Vice President of Novo Nordisk Quality, where you will also be part of the Novo Nordisk Quality Management team.
Qualifications
You have a relevant educational background, e.g., MD, PhD or master’s degree in pharmacy, natural sciences or engineering and extensive experience within drug and biologic development as well as:
About the area
R&D Quality is a growing, dynamic area with responsibility for assuring quality across both the Research and Early Development and the Development organisation. We are over 130 dedicated colleagues divided into 4 different areas, R&D Quality Operations, Clinical Quality, Global Safety Regulatory Affairs & IT Quality and Device and Delivery Solutions Quality. You will be part of a high performing culture with focus on quality, patient safety, cross-functional collaboration and both personal growth and professional development. We are passionate about reaching ambitious goals as a team, we are curious and courageous, always striving for simplicity and we believe in developing people through trust and empowerment.
Contact
To learn more about the position, well qualified candidates are welcome to contact Robin Evers on +45 30795206 between 17th- 21st July. No agency calls please.
Deadline for applications
4 August 2023 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.
Information og data
Denne ledige stilling har jobtypen "Administrativ medarbejder", og befinder sig i kategorien "Kontor, handel og service".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 30.6.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Administrativ medarbejder
- Søborg
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