Validation and Quality Responsible for Equipment in OFP
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Måløv
In Oral Finished Products (OFP) at Målev, we set ourselves the ambitious goal of being the first on the market with a tablet containing a GLP-1 based drug. An ambitious goal has been achieved as the product has gained approval in several markets worldwide. With this ground-breaking tablet, Rybelsus®, we are extremely proud that we finally offer patients with type 2 diabetes an alternative to the injectable preparations.
Our next ambitious goal is to ramp up, to secure the overwhelming demand for Rybelsus® tablets for our patients. Therefore, we are pleased if you take the opportunity to join this exciting and ground-breaking journey that offers completely new possibilities for diabetes treatment.
So, do you want to help implement, validate and maintain equipment? Are you an academic with strong maintenance and validation skills, ready to take responsibility for keeping our operational equipment running in a manufacturing setup with very high-quality standards? If yes, then you could be our new equipment responsible.
About the department
OFP Production consists of approx. 230 dedicated employees in 2 areas; Bulk Tablet Production and Pack. The vacant position as Validation and Quality Responsible is part of the team Rybelsus Equipment Support, which consists of approx. 20 dedicated employees with responsibility for tablet production, where we focus on production for the market, ramp-up and optimization of our processes in close collaboration with the other teams in the Bulk area.
The position
As our new colleague, your days will be highly varied. You will be part of the equipment support team responsible for securing stable performance for a variety of equipment in the tablet production such as tablet press, V-shell blenders, roller compactors and IPC equipment. Your job will also be focusing on optimization and maintenance of the equipment and the validated state in close collaboration with your highly skilled and dedicated colleagues. We highly prioritize presence in the production facility and good collaboration with operators and technicians.
You will be appointed responsible for specific equipment and must ensure that the equipment is ready for production within the pharmaceutical industry's requirements. You will be a part of the daily support with expert knowledge for handling incidents, change requests, deviations, and projects. Your expertise will be needed for systematic problem solving (A3) – ensuring that we find the correct root cause on which we can base corrective and preventive measures. At other times, optimizations and projects will be your focus – making sure that we will be able to meet the growing demands of the future.
In OFP, we make a significant effort to ensure that you as a new employee get the best possible start in your new job. Therefore, you will go through an exciting introductory course and a colleague from your own team will act as a mentor and review your individual training plan.
Qualifications
As our work is carried out and documented in accordance with GMP regulations, a systematic approach and a strong quality mindset is expected to be successful in the role we expect you to have:
You will work closely with different professional groups, so good collaboration and communication skills are highly valued. On a personal level you are result-oriented, good at planning and you take pride in driving tasks forward and meeting deadlines. We also emphasize that you are a team-player with a good sense of humour and that you can motivate others around you. In our team we prioritize a social and relaxed atmosphere.
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 are all working to move the needle on patient care.
Contact
For questions about the position, please contact Associate Manager Jan Kristiansen at +45 3079 6809.
Deadline
11 December 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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Our next ambitious goal is to ramp up, to secure the overwhelming demand for Rybelsus® tablets for our patients. Therefore, we are pleased if you take the opportunity to join this exciting and ground-breaking journey that offers completely new possibilities for diabetes treatment.
So, do you want to help implement, validate and maintain equipment? Are you an academic with strong maintenance and validation skills, ready to take responsibility for keeping our operational equipment running in a manufacturing setup with very high-quality standards? If yes, then you could be our new equipment responsible.
About the department
OFP Production consists of approx. 230 dedicated employees in 2 areas; Bulk Tablet Production and Pack. The vacant position as Validation and Quality Responsible is part of the team Rybelsus Equipment Support, which consists of approx. 20 dedicated employees with responsibility for tablet production, where we focus on production for the market, ramp-up and optimization of our processes in close collaboration with the other teams in the Bulk area.
The position
As our new colleague, your days will be highly varied. You will be part of the equipment support team responsible for securing stable performance for a variety of equipment in the tablet production such as tablet press, V-shell blenders, roller compactors and IPC equipment. Your job will also be focusing on optimization and maintenance of the equipment and the validated state in close collaboration with your highly skilled and dedicated colleagues. We highly prioritize presence in the production facility and good collaboration with operators and technicians.
You will be appointed responsible for specific equipment and must ensure that the equipment is ready for production within the pharmaceutical industry's requirements. You will be a part of the daily support with expert knowledge for handling incidents, change requests, deviations, and projects. Your expertise will be needed for systematic problem solving (A3) – ensuring that we find the correct root cause on which we can base corrective and preventive measures. At other times, optimizations and projects will be your focus – making sure that we will be able to meet the growing demands of the future.
In OFP, we make a significant effort to ensure that you as a new employee get the best possible start in your new job. Therefore, you will go through an exciting introductory course and a colleague from your own team will act as a mentor and review your individual training plan.
Qualifications
As our work is carried out and documented in accordance with GMP regulations, a systematic approach and a strong quality mindset is expected to be successful in the role we expect you to have:
- A scientific background, a Master's degree, for example a Cand. Scient, Cand. Pharm, Cand. Polyt. or similar, but over all a curiosity for pharmaceutical production.
- Preferably, +3 years of experience with maintenance and validation from the pharmaceutical or other regulated industry, together with insight into GMP regulation. If you have newly graduated (or in the process of finishing your thesis) you are welcome to apply, but you should be curious to learn and be prepared for a steep learning curve.
- A Go-Look-See mindset and collaboration skills across different teams and roles.
- Experience in working with change requests, requirement specifications, validation, and test, as well as deviations will be an advantage.
- Good Danish and English language skills.
You will work closely with different professional groups, so good collaboration and communication skills are highly valued. On a personal level you are result-oriented, good at planning and you take pride in driving tasks forward and meeting deadlines. We also emphasize that you are a team-player with a good sense of humour and that you can motivate others around you. In our team we prioritize a social and relaxed atmosphere.
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 are all working to move the needle on patient care.
Contact
For questions about the position, please contact Associate Manager Jan Kristiansen at +45 3079 6809.
Deadline
11 December 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 Måløv.
Jobbet er oprettet på vores service den 13.8.2022, 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
- Måløv
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