Quality Supporter
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Kalundborg
Improvement oriented Quality coordinator with the right mindset in Novo Nordisk PS API Are compliance and efficiency core values for you as an individual? Are you always ready to initiate and join activities that will elevate the level of quality and compliance by applying LEAN principles? Do you enjoy analysing data to spot trends that call for action? If you say yes to the above, we would like to welcome you in IM2 (Insulin Manufacturing 2) Purification, as we are looking for a talented Quality Coordinator.
The position
As Quality Coordinator you are part of the department’s staff function. In collaboration with the management-team you drive the quality and compliance agenda of the department. Together with a network of Quality Coordinators from other departments in IM2 you drive audits and inspections, you ensure overall inspection readiness and provide training within cGMP for the organisation. Your daily tasks include sparring, training, and coaching of employees as well as leaders across the department. As Quality Coordinator for the department, we expect you to be the “go to” person on quality subjects.
In the department we strive to be more agile, to think bigger and to cut complexity. You will be involved in relevant projects to ensure quality is built in simultaneously with development and implementation of new technology.
At Novo Nordisk quality and LEAN is tightly linked together. As part of daily operation, you will help improving the quality in the department. Your main tasks will be
• To support to the Quality Management System (QMS) by ensuring compliance of the department procedures to existing and upcoming requirements. • To perform trend analysis on key KPI’s to spot improvement projects in the department. • To participate in the IM2 Quality Coordinator network and to coordinate input to the Quality Management Review on behalf of the department • To join the planning, preparation, and execution of audits in IM2/API • To drive Quality improvement initiatives applying PDCA (Plan Do Check Act), systematic problem solving (A3s), process mapping (VSM’s) or other LEAN methodologies. • To participate in reduction of deviations. Qualifications
To succeed in this role, you hold an academic degree as Engineer, Pharmacist, or another degree within natural science. Have a well-developed Quality Mindset and have at least 2 years of experience within Good Manufacturing Practice (GMP). In addition, we will look for candidate that:
• Have experience with quality and GMP requirements applicable to a production environment. Take responsibility, work independently, and make decisions that balance quality requirements, authority expectations and business needs. • Demonstrate a LEAN mindset and possess project management skills. • Organise your time and tasks to keep your deadlines. You try to solve issues on your own, but do not hesitate to ask for support when that is required to secure success in your deliveries. • Have excellent communication and collaboration skills and are fluent in English and Danish • Additionally, we would enjoy welcoming a straightforward person with a good sense of humour to our department. About the department
You will join Purification, IM2 in Kalundborg, Denmark. We are approximately 150 colleagues, working in 6 teams. We produce Human Insulin, which play a significant role in Novo Nordisk’s social responsibility strategy. We deliver massive quantities to third world countries. We are dedicated to deliver strong results that add to the success of Novo Nordisk in crucial ways by ensuring high quality API at a competitive cost for our patients. We share a relaxed tone and big ambitions, and we are proud to never compromise on quality or safety. Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at various stages of our career is never easy. That is why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it is a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we are life changing.
Contact
If you have any questions about the job, please do not hesitate to call Director Kathrine Holm Juliussen +4530752599.
Deadline
Please apply before 27th January 2023. Interviews will be conducted on an ongoing basis.
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.
The position
As Quality Coordinator you are part of the department’s staff function. In collaboration with the management-team you drive the quality and compliance agenda of the department. Together with a network of Quality Coordinators from other departments in IM2 you drive audits and inspections, you ensure overall inspection readiness and provide training within cGMP for the organisation. Your daily tasks include sparring, training, and coaching of employees as well as leaders across the department. As Quality Coordinator for the department, we expect you to be the “go to” person on quality subjects.
In the department we strive to be more agile, to think bigger and to cut complexity. You will be involved in relevant projects to ensure quality is built in simultaneously with development and implementation of new technology.
At Novo Nordisk quality and LEAN is tightly linked together. As part of daily operation, you will help improving the quality in the department. Your main tasks will be
• To support to the Quality Management System (QMS) by ensuring compliance of the department procedures to existing and upcoming requirements. • To perform trend analysis on key KPI’s to spot improvement projects in the department. • To participate in the IM2 Quality Coordinator network and to coordinate input to the Quality Management Review on behalf of the department • To join the planning, preparation, and execution of audits in IM2/API • To drive Quality improvement initiatives applying PDCA (Plan Do Check Act), systematic problem solving (A3s), process mapping (VSM’s) or other LEAN methodologies. • To participate in reduction of deviations. Qualifications
To succeed in this role, you hold an academic degree as Engineer, Pharmacist, or another degree within natural science. Have a well-developed Quality Mindset and have at least 2 years of experience within Good Manufacturing Practice (GMP). In addition, we will look for candidate that:
• Have experience with quality and GMP requirements applicable to a production environment. Take responsibility, work independently, and make decisions that balance quality requirements, authority expectations and business needs. • Demonstrate a LEAN mindset and possess project management skills. • Organise your time and tasks to keep your deadlines. You try to solve issues on your own, but do not hesitate to ask for support when that is required to secure success in your deliveries. • Have excellent communication and collaboration skills and are fluent in English and Danish • Additionally, we would enjoy welcoming a straightforward person with a good sense of humour to our department. About the department
You will join Purification, IM2 in Kalundborg, Denmark. We are approximately 150 colleagues, working in 6 teams. We produce Human Insulin, which play a significant role in Novo Nordisk’s social responsibility strategy. We deliver massive quantities to third world countries. We are dedicated to deliver strong results that add to the success of Novo Nordisk in crucial ways by ensuring high quality API at a competitive cost for our patients. We share a relaxed tone and big ambitions, and we are proud to never compromise on quality or safety. Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at various stages of our career is never easy. That is why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it is a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we are life changing.
Contact
If you have any questions about the job, please do not hesitate to call Director Kathrine Holm Juliussen +4530752599.
Deadline
Please apply before 27th January 2023. Interviews will be conducted on an ongoing basis.
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.
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 4.1.2023, 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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