Environmental Monitoring Responsible
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Kalundborg
Are you looking for a career opportunity where you unfold your skills within the workflow process of Environmental Monitoring (EM) for our new factory in Kalundborg? We are expanding to provide capacity for the production of Novo Nordisk’s current and future oral and injectable products by establishing new and ground-breaking biotech facility in Novo Nordisk Kalundborg. Now is your opportunity to join a newly established team, where you will be able to improve and exercise your technical and analytical skills.
The Position
You will be responsible for fulfilling a high level of Quality within the technical area of Environmental Management (EM) in close cooperation with the project team and project managers. You will play a key role for our ability to be operational ready within EM, ensure preparation and completion of various qualification tasks. Later when the project transfers from project to operations, you will also work with periodic EM systems reviews, change requests, standard operating procedures and protocols to support future improvement projects. On top of that you can support within environmental monitoring in general and conduct data clarifications and root cause analysis. It is a vital success criterion to enhance and standardise the system compliance in regard to documentation and improve the analytical approach with data based investigations.
Qualifications
Academic background – GMP knowledge as well as microbiology is an advantage. You have a relevant degree at bachelor level or similar, for instance as an Bsc. Or Msc. in Natural Science, engineering. Maybe you only have few years of experience and are a quick learner.
Your personal qualities define you as structured, self-starting and capable of finalising tasks with a high level of quality mind set. In your daily challenges you have the personal skills of understanding complex systems, subsequently define necessary arrangements and set direction with the right level of GMP focus.
In addition, you have the ability of understanding requirements for working with classified room areas or HVAC systems. Last but not least, you have proficiency in writing various documents related to quality activities within the area of responsibility of the team. Documents will be prepared in Danish most of the time.
About the Department
We are currently building a new factory and our department will continue to expand over the coming years as we go from project phase to production. In this new team, you will be collaborating closely with colleagues with backgrounds within chemistry, engineering, project management, automation and facility planning.
We know that a diverse group of people, performs the best results, and we are eager to build teams where collaboration across professional backgrounds ensures a right first-time execution of highly complex projects. You will play a vital role in building and maintaining a healthy and inspiring work culture and have an abundance of opportunities for professional and personal development.
Working at Novo Nordisk
BRD Active Pharmaceutical Ingredient (API) Denmark is located in Gentofte, Hilleroed and Kalundborg. This is where the active ingredients, going into all our life-saving biotech products, are made by app. 500 committed colleagues. We manufacture through complex chemical and biotechnological processes requiring a high level of expertise, commitment, and engagement from our employees and including cultivation, recovery, purification and freeze-drying. We are producing at full speed in existing facilities, while building and ramping up new state of the art additions to keep up with demand and new Novo Nordisk products. We bring value to patients by delivering the purest possible high-quality API made in compliance with Good Manufacturing Process (GMP). We drive change by always looking for improvements within our processes, but also in the way we work together to make our products reach as many patients as possible.
Contact
For further information, please contact Morten Lomholt, +45 30 75 35 66
Deadline
20 November, 2022.
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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The Position
You will be responsible for fulfilling a high level of Quality within the technical area of Environmental Management (EM) in close cooperation with the project team and project managers. You will play a key role for our ability to be operational ready within EM, ensure preparation and completion of various qualification tasks. Later when the project transfers from project to operations, you will also work with periodic EM systems reviews, change requests, standard operating procedures and protocols to support future improvement projects. On top of that you can support within environmental monitoring in general and conduct data clarifications and root cause analysis. It is a vital success criterion to enhance and standardise the system compliance in regard to documentation and improve the analytical approach with data based investigations.
Qualifications
Academic background – GMP knowledge as well as microbiology is an advantage. You have a relevant degree at bachelor level or similar, for instance as an Bsc. Or Msc. in Natural Science, engineering. Maybe you only have few years of experience and are a quick learner.
Your personal qualities define you as structured, self-starting and capable of finalising tasks with a high level of quality mind set. In your daily challenges you have the personal skills of understanding complex systems, subsequently define necessary arrangements and set direction with the right level of GMP focus.
In addition, you have the ability of understanding requirements for working with classified room areas or HVAC systems. Last but not least, you have proficiency in writing various documents related to quality activities within the area of responsibility of the team. Documents will be prepared in Danish most of the time.
About the Department
We are currently building a new factory and our department will continue to expand over the coming years as we go from project phase to production. In this new team, you will be collaborating closely with colleagues with backgrounds within chemistry, engineering, project management, automation and facility planning.
We know that a diverse group of people, performs the best results, and we are eager to build teams where collaboration across professional backgrounds ensures a right first-time execution of highly complex projects. You will play a vital role in building and maintaining a healthy and inspiring work culture and have an abundance of opportunities for professional and personal development.
Working at Novo Nordisk
BRD Active Pharmaceutical Ingredient (API) Denmark is located in Gentofte, Hilleroed and Kalundborg. This is where the active ingredients, going into all our life-saving biotech products, are made by app. 500 committed colleagues. We manufacture through complex chemical and biotechnological processes requiring a high level of expertise, commitment, and engagement from our employees and including cultivation, recovery, purification and freeze-drying. We are producing at full speed in existing facilities, while building and ramping up new state of the art additions to keep up with demand and new Novo Nordisk products. We bring value to patients by delivering the purest possible high-quality API made in compliance with Good Manufacturing Process (GMP). We drive change by always looking for improvements within our processes, but also in the way we work together to make our products reach as many patients as possible.
Contact
For further information, please contact Morten Lomholt, +45 30 75 35 66
Deadline
20 November, 2022.
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.
Print job Send to e-mail
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 11.10.2022, 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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