Senior Project Manager
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Do you want to be at the forefront of driving the improvement technology agenda in our tablet productions and QC area? Do you enjoy managing dynamic and challenging projects and collaborating with diverse global stakeholders? If yes, then you could be our new Senior Project Manager for Process Analytical Technology (PAT) implementation. Read more below and apply for a life-changing career! The position This position as Senior Project Manager is a unique opportunity where you will be responsible for managing cross-organizational PAT projects with the main aim of designing and implementing PAT in operations. You will work closely together with the PAT specialists, process teams, IT/OT organization, and quality across our organisation. Areas of responsibility will include:
•Liaise, where necessary, with key stakeholders such as process engineers, data modelers, analytical scientists, quality assurance and PAT vendors
•Facilitating and owning operational risk assessment
•Ensure standards are being followed and continuously updated based on new experiences with PAT
•Support and impact the organizational journey and change management process that we are faced with due to the implementation of new technologies
Qualifications To be successful in this position, you will need:
•Bachelor’s or Master’s degree within science, engineering, or a similar scientific field
•Experience with PAT from development or production
•Solid experience with project management within the pharmaceutical or similar industry
•Excellent stakeholder management skills
•Ability to communicate complex content in a simple way
•Fluency in written and spoken English Having Project Management certification, e.g., PMP® or PRINCE2® would be beneficial. As a person, you set high standards for your work, and you are data-driven. You are a team player who works well managing complex dependencies between different areas in a structured way. Your curious mind can challenge the status quo in a positive way. About the department Emerging Technologies (ET) is a newly established SVP area in Novo Nordisk. We have a growing pipeline of new products, many of which are based on emerging technology platforms coming into Product Supply via internal development projects and externally acquired assets. ET are well-known for having a pioneering spirit as well as a curious and daring approach and we play a key role in developing and producing future treatments for millions of patients around the world. You will be joining the VP area Drug Product Manufacturing Development & Quality Control (DP MDev & QC), which has process and product responsibility for existing and future oral drug products post-launch, as well as performing all analyses on products after method transfer. We work across the ET organization to improve productivity of our production and analytical processes. The area currently consists of 5 departments and is expanding to prepare for new drug products. 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. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact If you have any questions, please contact Snr. Manager, Mie Houlberg Danielsen at +45 3448 8695 Deadline 3 January 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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.
•Liaise, where necessary, with key stakeholders such as process engineers, data modelers, analytical scientists, quality assurance and PAT vendors
•Facilitating and owning operational risk assessment
•Ensure standards are being followed and continuously updated based on new experiences with PAT
•Support and impact the organizational journey and change management process that we are faced with due to the implementation of new technologies
Qualifications To be successful in this position, you will need:
•Bachelor’s or Master’s degree within science, engineering, or a similar scientific field
•Experience with PAT from development or production
•Solid experience with project management within the pharmaceutical or similar industry
•Excellent stakeholder management skills
•Ability to communicate complex content in a simple way
•Fluency in written and spoken English Having Project Management certification, e.g., PMP® or PRINCE2® would be beneficial. As a person, you set high standards for your work, and you are data-driven. You are a team player who works well managing complex dependencies between different areas in a structured way. Your curious mind can challenge the status quo in a positive way. About the department Emerging Technologies (ET) is a newly established SVP area in Novo Nordisk. We have a growing pipeline of new products, many of which are based on emerging technology platforms coming into Product Supply via internal development projects and externally acquired assets. ET are well-known for having a pioneering spirit as well as a curious and daring approach and we play a key role in developing and producing future treatments for millions of patients around the world. You will be joining the VP area Drug Product Manufacturing Development & Quality Control (DP MDev & QC), which has process and product responsibility for existing and future oral drug products post-launch, as well as performing all analyses on products after method transfer. We work across the ET organization to improve productivity of our production and analytical processes. The area currently consists of 5 departments and is expanding to prepare for new drug products. 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. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact If you have any questions, please contact Snr. Manager, Mie Houlberg Danielsen at +45 3448 8695 Deadline 3 January 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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.
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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 7.12.2023, 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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