Director of Technology and Innovation
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Måløv
Are you our new strategic leader who can build and develop the future QC Innovation strategy? Are you a passionate leader who can lead, coach, and develop a skilled team? Are you passionate about technology? As our new Director of the Analytical Technology & Innovation Department, you provide new, innovative solutions every day.
The position
We are looking for a leader who has technology and innovation in the blood, and who can build and execute the technology and innovation strategy by heading up – and developing - the team with a focus on improving QC capacity and productivity.
You will set the strategic direction and deploy new technology solutions that increase QC performance and helps production meet our capacity and development demands.
You will head up the Oral Finished Products (OFP) Analytical Technology and Innovation department which consists of 3 teams – responsible for existing and novel OFP QC equipment as well as Innovation Solutions that can serve as means to improve QC performance, such as Real-time performance visualization, Machine Learning, Artificial Intelligence, Automation, etc. You will be responsible for the OFP QC ambitions in developing cross-functional automated and digital QC solutions to increase productivity.
The role and responsibilities:
• Responsible for the roadmap and implementation of innovation activities including setting direction for the digitalization and automation journey across OFP QC, • Ensuring success by hiring core competencies within data scientists, project managers and technicians with talent and competencies within digitalization and automation • Driving a department capable of identifying and managing innovation activities in the OFP QC area such as paperless QC, robotic process automation, etc. • Facilitating and driving a rollout of Quality Control solutions across neighboring QC departments to ensure continued productivity and quality improvements • Liaising with other Novo Nordisk units within Manufacturing Intelligence, Advanced Analytics, Artificial Intelligence, Machine Learning, and other relevant Digital Production Enhancement tools. You will also be identifying and managing a portfolio of development projects in close collaboration with other QC areas, production sites, IT, and relevant units with relevant capabilities. The portfolio of activities ranges from simple evolution of existing solutions to Industry First’s advanced and revolutionary solutions. Qualifications:
You are an experienced and proactive leader who leads through others and sets clear strategic directions. You have demonstrated the ability to manage complex projects, cross-functional teams, and global experience.
You hold a master’s degree/Ph.D. or similar and you have several years of international GMP-relevant experience from quality control or production. You do not need QC experience, but at a minimum, you understand the analytical field preferably from the pharmaceutical industry. You have a proven track record in running a portfolio of projects successfully as well as building and maintaining relationships and networks on a global level and with higher-ranking stakeholders. You are comfortable being challenged by senior stakeholders and your high level of personal integrity and robustness enables you to integrate different views into the decision making process. On a personal level, you have a high level of integrity, credibility, personal engagement, and energy. Moreover, you can motivate and make all participants focus on the promised deadlines. Leadership style must be open and honest with a strong focus on cultural differences. You are result oriented with a broad business understanding and high analytical skills. You have the ability to handle high-pressure and conflicting interests without stress. Fluency in English, written and verbal on a technical level is required.
About the Area
OFP QC employs 200 skilled lab technicians, scientists, and chemists. In QC we provide fast efficient and reliable analytical results from phase 3 to market. We also provide analytical support to OFP Manufacturing Development and secure method validation at project transfer. As Director of OFPQC AT&I you will be responsible for 40 employees and 6 direct reports including an agile team developing a digitalization solution on behalf of all Novo Nordisk laboratories. You will report to the VP of OFP QC and work closely with Directors of QC New Product Entry and QC Market Release.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them.
Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life-changing. Contact
If you have any questions, you are welcome to reach out to VP QC Pia Bru Petersen, at +45 3075 3031.
Deadline 28th of February 2023
Send your application soon as we call for interviews on an ongoing basis. 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.
The position
We are looking for a leader who has technology and innovation in the blood, and who can build and execute the technology and innovation strategy by heading up – and developing - the team with a focus on improving QC capacity and productivity.
You will set the strategic direction and deploy new technology solutions that increase QC performance and helps production meet our capacity and development demands.
You will head up the Oral Finished Products (OFP) Analytical Technology and Innovation department which consists of 3 teams – responsible for existing and novel OFP QC equipment as well as Innovation Solutions that can serve as means to improve QC performance, such as Real-time performance visualization, Machine Learning, Artificial Intelligence, Automation, etc. You will be responsible for the OFP QC ambitions in developing cross-functional automated and digital QC solutions to increase productivity.
The role and responsibilities:
• Responsible for the roadmap and implementation of innovation activities including setting direction for the digitalization and automation journey across OFP QC, • Ensuring success by hiring core competencies within data scientists, project managers and technicians with talent and competencies within digitalization and automation • Driving a department capable of identifying and managing innovation activities in the OFP QC area such as paperless QC, robotic process automation, etc. • Facilitating and driving a rollout of Quality Control solutions across neighboring QC departments to ensure continued productivity and quality improvements • Liaising with other Novo Nordisk units within Manufacturing Intelligence, Advanced Analytics, Artificial Intelligence, Machine Learning, and other relevant Digital Production Enhancement tools. You will also be identifying and managing a portfolio of development projects in close collaboration with other QC areas, production sites, IT, and relevant units with relevant capabilities. The portfolio of activities ranges from simple evolution of existing solutions to Industry First’s advanced and revolutionary solutions. Qualifications:
You are an experienced and proactive leader who leads through others and sets clear strategic directions. You have demonstrated the ability to manage complex projects, cross-functional teams, and global experience.
You hold a master’s degree/Ph.D. or similar and you have several years of international GMP-relevant experience from quality control or production. You do not need QC experience, but at a minimum, you understand the analytical field preferably from the pharmaceutical industry. You have a proven track record in running a portfolio of projects successfully as well as building and maintaining relationships and networks on a global level and with higher-ranking stakeholders. You are comfortable being challenged by senior stakeholders and your high level of personal integrity and robustness enables you to integrate different views into the decision making process. On a personal level, you have a high level of integrity, credibility, personal engagement, and energy. Moreover, you can motivate and make all participants focus on the promised deadlines. Leadership style must be open and honest with a strong focus on cultural differences. You are result oriented with a broad business understanding and high analytical skills. You have the ability to handle high-pressure and conflicting interests without stress. Fluency in English, written and verbal on a technical level is required.
About the Area
OFP QC employs 200 skilled lab technicians, scientists, and chemists. In QC we provide fast efficient and reliable analytical results from phase 3 to market. We also provide analytical support to OFP Manufacturing Development and secure method validation at project transfer. As Director of OFPQC AT&I you will be responsible for 40 employees and 6 direct reports including an agile team developing a digitalization solution on behalf of all Novo Nordisk laboratories. You will report to the VP of OFP QC and work closely with Directors of QC New Product Entry and QC Market Release.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them.
Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life-changing. Contact
If you have any questions, you are welcome to reach out to VP QC Pia Bru Petersen, at +45 3075 3031.
Deadline 28th of February 2023
Send your application soon as we call for interviews on an ongoing basis. 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 2.2.2023, 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.
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