QA Professional - Production, QC or IT
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Are you seeking new challenges or maybe you are a newly graduated that are ready to start your career? If, yes, then this might be the job for you. We are currently looking for a QA Professional to join the QA Operations team at Novo Nordisk Pharmatech A/S in Køge.
Working in our team you will have both great professional and personal development opportunities. We can offer you a great working environment with a high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. The position Due to an increasing demand of both current production as well as new products, we are looking for a new QA Professional to join the team. In the role, you are responsible for setting direction for our quality system and ensuring compliance with the requirements from both customers and authorities around the world. You will coordinate several tasks with different deadlines in a dynamic and flexible team. To succeed in this job, it is important to have a close and good collaboration with your colleagues in production and be able to communicate with a wide range of people. Your primary responsibilities will be approval of deviations, change requests, release of products and qualification and validation documentation related to the production. Furthermore, there may be a possibility to be involved in approval of documents related to QC and IT operations and to be trained in internal and customer audits. In the coming years Novo Nordisk Pharmatech A/S has various projects in the pipeline, so you may also be involved as QA responsible in both minor and major projects. These projects cover implementation of new equipment, changing the existing processes and reconstruction of facilities to production of new products. We offer an exciting and challenging position in an amazing department where focus on collaboration and team spirit are key. As a new member of the team, we will prioritize your training and support you in gaining the competencies needed. Qualifications To succeed in this role, you have: A master’s degree in pharmacy, engineering or similar Experience from QA, QC, Production Support or similar will be an advantage but not a requirement Experience with good manufacturing practice (GMP) Great interpersonal as well as communication skills As a person, you have an innovative mind-set and the ability to work effectively in a team-oriented setting. Openness, honesty, curiosity to learn and focus on continuous improvements and quality mindset are natural parts of your personality and the way you work. You have a can-do attitude and focus on opportunities rather than on limitations. About the department Novo Nordisk Pharmatech A/S is a fully owned subsidiary of Novo Nordisk A/S situated in Køge. Novo Nordisk Pharmatech A/S is a leading global supplier of high-quality ingredients for the biopharmaceutical and pharmaceutical industries, supplying products such as recombinant insulin for cell growth media and pharmaceutical grade quaternary ammonium compounds as well as raw materials for Novo Nordisk A/S. QA Operations team is a part of the QA/RA department at Novo Nordisk Pharmatech A/S. QA/RA department currently consists of 25 employees working diligently to support the entire value chain, from Research & Development to Production and finally Sales & Marketing. We also cover quality and regulatory affairs related communication with the authorities, our B2B customers, our distributors, and our suppliers. Working at Novo Nordisk Pharmatech Novo Nordisk Pharmatech A/S has approximately 400 employees and is 100% owned by Novo Nordisk A/S. The ability of Novo Nordisk Pharmatech A/S to produce and deliver quality products to the pharmaceutical industry, combined with our complete range of services within the regulatory requirements, makes us a preferred supplier to many global pharmaceutical companies. Novo Nordisk Pharmatech A/S is a growing company, which will provide many exciting projects in the future and good development opportunities in the job. Contact For further information, you can contact Associate Manager, Daniel Grundahl, on +45 31 97 00 09. Deadline
February 11th 2024. You do not need to attach a cover letter to your application, but please include a few sentences about your motivation in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. novonordisk.papirfly.com/readimage.aspx/asset.mp4?pubid=VtFlwVFsztejayHeAcn7pg 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.
Working in our team you will have both great professional and personal development opportunities. We can offer you a great working environment with a high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. The position Due to an increasing demand of both current production as well as new products, we are looking for a new QA Professional to join the team. In the role, you are responsible for setting direction for our quality system and ensuring compliance with the requirements from both customers and authorities around the world. You will coordinate several tasks with different deadlines in a dynamic and flexible team. To succeed in this job, it is important to have a close and good collaboration with your colleagues in production and be able to communicate with a wide range of people. Your primary responsibilities will be approval of deviations, change requests, release of products and qualification and validation documentation related to the production. Furthermore, there may be a possibility to be involved in approval of documents related to QC and IT operations and to be trained in internal and customer audits. In the coming years Novo Nordisk Pharmatech A/S has various projects in the pipeline, so you may also be involved as QA responsible in both minor and major projects. These projects cover implementation of new equipment, changing the existing processes and reconstruction of facilities to production of new products. We offer an exciting and challenging position in an amazing department where focus on collaboration and team spirit are key. As a new member of the team, we will prioritize your training and support you in gaining the competencies needed. Qualifications To succeed in this role, you have:
February 11th 2024. You do not need to attach a cover letter to your application, but please include a few sentences about your motivation in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. novonordisk.papirfly.com/readimage.aspx/asset.mp4?pubid=VtFlwVFsztejayHeAcn7pg 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 Køge.
Jobbet er oprettet på vores service den 11.1.2024, 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.
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