Quality Coordinator
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Kalundborg
Do you have passion for quality, and are you motivated by setting compliance standards and ensuring that we continuously simplify and improve our processes and ways of working? Then, this is your chance to take the next step in your career and gain more responsibility for processes and quality in our expanding area.
The job It is an exciting and challenging position with a wide variety of tasks and many different stakeholders. It is therefore a prerequisite that you can work independently and have the ability to collaborate with various groups of employees with different backgrounds. Key tasks: Provide support and work as sparring partner on quality matters to ensure compliance with existing and new requirements Identify trends and possibilities for improvements across the department, that can reduce complexity and build quality and robustness into the processes Prepare the department for internal audits and inspections Plan and host training in GMP and QMS Attend in the preparation of quality oversight tools, trending reports, Quality Management Review etc. As quality coordinator you will be a part of the department’s management team and refer to the department manager. You will also have the possibility to be a member of the cross functional process groups, setting direction for quality management across API. Qualifications You hold a master’s degree within chemistry, life sciences or another relevant field To succeed in the role, we expect that you have a good understanding of GMP and Quality in production from years of relevant experience in the Pharma industry. You have experience with some of the following processes: deviation handling, change requests, qualification and validation, environmental monitoring and quality control You are curious and able to see opportunities for improvement. You speak and write English and Danish About the department
You will be part of a dynamic business area in a constant development which produce Active Pharmaceutical Ingredients (API) for patients across the world. IM1 is located in JC, Kalundborg and the department consists of 230 employees split into 6 production teams and 3 Support teams and a staff function. You will be employed in the M1 Purification department that is a multiline facility. We share an informal tone and ambitions to be the best at what we do – and we are good at helping each other and share both challenges and victories alike. About Novo Nordisk Kalundborg Become a part of Novo Nordisk Manufacturing in Kalundborg and get a developing career among the most talented people in a successful company. Together, we make a real difference every day for more than 30 million people living with diabetes and other chronic diseases. We have 50 years of expertise in biotechnological production at Novo Nordisk in Kalundborg. Generations of employees have developed their professional qualifications, personal skills and careers at Novo Nordisk and have helped develop the production facility to become the largest insulin-producing facility in the world. Today, our 3,000 employees produce half of the world’s insulin and a number of biopharmaceutical products. Furthermore, our finished product sections assemble and pack diabetes and biopharmaceutical products. You will soon sense why Novo Nordisk Kalundborg is a highly unique place and why we are passionate about working here. You will be met with trust and responsibility by welcoming and dedicated colleagues. Contact If you have any questions regarding the position, please feel free to contact Director Brian Bech Daugaard at +45 30752759 or CVP Quality Coordinator Helle Lundberg Nielsen at +45 30757991. Deadline 15th January 2024 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. Please note that we will be reviewing applications on an ongoing basis and feel free to apply in Danish or English as you wish. 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 job It is an exciting and challenging position with a wide variety of tasks and many different stakeholders. It is therefore a prerequisite that you can work independently and have the ability to collaborate with various groups of employees with different backgrounds. Key tasks:
You will be part of a dynamic business area in a constant development which produce Active Pharmaceutical Ingredients (API) for patients across the world. IM1 is located in JC, Kalundborg and the department consists of 230 employees split into 6 production teams and 3 Support teams and a staff function. You will be employed in the M1 Purification department that is a multiline facility. We share an informal tone and ambitions to be the best at what we do – and we are good at helping each other and share both challenges and victories alike. About Novo Nordisk Kalundborg Become a part of Novo Nordisk Manufacturing in Kalundborg and get a developing career among the most talented people in a successful company. Together, we make a real difference every day for more than 30 million people living with diabetes and other chronic diseases. We have 50 years of expertise in biotechnological production at Novo Nordisk in Kalundborg. Generations of employees have developed their professional qualifications, personal skills and careers at Novo Nordisk and have helped develop the production facility to become the largest insulin-producing facility in the world. Today, our 3,000 employees produce half of the world’s insulin and a number of biopharmaceutical products. Furthermore, our finished product sections assemble and pack diabetes and biopharmaceutical products. You will soon sense why Novo Nordisk Kalundborg is a highly unique place and why we are passionate about working here. You will be met with trust and responsibility by welcoming and dedicated colleagues. Contact If you have any questions regarding the position, please feel free to contact Director Brian Bech Daugaard at +45 30752759 or CVP Quality Coordinator Helle Lundberg Nielsen at +45 30757991. Deadline 15th January 2024 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. Please note that we will be reviewing applications on an ongoing basis and feel free to apply in Danish or English as you wish. 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 20.12.2023, 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.
- Øvrige
- Kalundborg
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