Associate Manager for Qualification and User Manager
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Kalundborg
Are you a highly motivated leader, driven by complex challenges and a broad area of responsibility? Are you motivated by challenges requiring a high level of professional competencies and leadership experience? Are you passionate about working with people and make them succeed in a complex environment with diverse stakeholder groups?Then you may be the new colleague we are looking for in IM1, Kalundborg. The position
You will be the Associate Manager for the team with technical experts within Qualification and Validation. The team consists of internal employees and consultants.
In addition to your role as Associate Manager you will also have a role as Usermanager in the matrix organization – a complex role with many stakeholders. You and the team is responsible for supporting projects from early idea phase to implementation in the factory, driving tasks and setting the direction within qualification and validation. The amount of stakeholders to manage is high, and we create fantastic results, by cooperation and communication across the organization. As a leader you will have a central position in the team, but also within the department and other parts of the organisation primarily Production, Quality and Engineering teams. Your tasks will be diverse ranging from: · Coordination of daily activities · Balancing resources · Overseeing and following up on projects · Managing staffing in the Q group with consultants · Supporting our journey within Qualification and Validation However, your main and equally important task will include you being an engaged, involving and present leader for your employees, where you need to balance short term needs with long term development of both the individual and the team. Qualifications
You have solid experience leading highly qualified professionals and probably you have a background as BSc/MSc within Pharmacy, Chemical Engineering, Chemistry/Biology or similar. Preferably with experience from the pharmaceutical or medical device industry or similarly related areas. · It’s important that you can think and act with a broad and strategic perspective, seeing “The Big Picture” without losing sight or interest in important details · You are familiar and confident with complex production processes · You have experience from GMP regulated areas · Experience with project management from GMP regulated areas will be a plus · You are fluent verbally and in writing in English as well as Danish As an individual you are positive, corporative, action and solution orientated, and you work systematically, logically and proactive. You are robust and capable of handling a, from time to time, high and complex work-pace without losing the overview and motivation. As a leader, you see and respect the individual and naturally adapt your leadership style to the competences, experience, engagement and need of the individual employee from both a business and personal perspective. About the department
IM1 Projects is responsible for the investment portfolio and execution of projects in the production facilities. The department is organized in a matrix with approx. 160 colleagues executing the portfolio, consisting of many projects in different phases. Working at Novo Nordisk 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 the communities we operate in. Contact
If you want to know more about the position, please contact Director Steffan Christensen at +45 3075 6145. Deadline
July, 15. Please note that applications will be reviewed after the deadline. 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.
You will be the Associate Manager for the team with technical experts within Qualification and Validation. The team consists of internal employees and consultants.
In addition to your role as Associate Manager you will also have a role as Usermanager in the matrix organization – a complex role with many stakeholders. You and the team is responsible for supporting projects from early idea phase to implementation in the factory, driving tasks and setting the direction within qualification and validation. The amount of stakeholders to manage is high, and we create fantastic results, by cooperation and communication across the organization. As a leader you will have a central position in the team, but also within the department and other parts of the organisation primarily Production, Quality and Engineering teams. Your tasks will be diverse ranging from: · Coordination of daily activities · Balancing resources · Overseeing and following up on projects · Managing staffing in the Q group with consultants · Supporting our journey within Qualification and Validation However, your main and equally important task will include you being an engaged, involving and present leader for your employees, where you need to balance short term needs with long term development of both the individual and the team. Qualifications
You have solid experience leading highly qualified professionals and probably you have a background as BSc/MSc within Pharmacy, Chemical Engineering, Chemistry/Biology or similar. Preferably with experience from the pharmaceutical or medical device industry or similarly related areas. · It’s important that you can think and act with a broad and strategic perspective, seeing “The Big Picture” without losing sight or interest in important details · You are familiar and confident with complex production processes · You have experience from GMP regulated areas · Experience with project management from GMP regulated areas will be a plus · You are fluent verbally and in writing in English as well as Danish As an individual you are positive, corporative, action and solution orientated, and you work systematically, logically and proactive. You are robust and capable of handling a, from time to time, high and complex work-pace without losing the overview and motivation. As a leader, you see and respect the individual and naturally adapt your leadership style to the competences, experience, engagement and need of the individual employee from both a business and personal perspective. About the department
IM1 Projects is responsible for the investment portfolio and execution of projects in the production facilities. The department is organized in a matrix with approx. 160 colleagues executing the portfolio, consisting of many projects in different phases. Working at Novo Nordisk 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 the communities we operate in. Contact
If you want to know more about the position, please contact Director Steffan Christensen at +45 3075 6145. Deadline
July, 15. Please note that applications will be reviewed after the deadline. 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 Kalundborg.
Jobbet er oprettet på vores service den 13.6.2023, 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.
- Øvrige
- Kalundborg
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Statistik over udbudte øvrige i Kalundborg over tid
| Dato | Alle jobs som øvrige |
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