Senior QA Professional
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Senior QA professional to Supply Chain QA – focusing on Master Data Are you ready to ensure compliance and high quality in the supply chain of Novo Nordisk products produced worldwide? Do you want to cooperate with stakeholders all over the world? Are you interested in Master Data and data integrity and want to set direction for how Novo Nordisk works with Master Data in the future? Then we may have just the right job for you in Supply Chain QA.
About the department
Supply Chain QA is responsible for Quality Assurance and support of Supply Chain Planning and Logistic activities including cold chain distribution of Novo Nordisk products worldwide, production planning across the entire Novo Nordisk supply chain, and data management and governance across Novo Nordisk. The department has 18 employees and is expected to grow in the coming years.
In our daily work we work closely together with Supply Chain Planning & Logistic (SCP&L) – our Line of Business, whom we support in quality matters, are involved in high impact projects, and set quality direction for. You will become part of a team focusing on the digital part of our supply chain incl. master data and planning processes. It is a team which have a high level of self-governance, good working relations, are informal and value professional sparring and good humour highly.
The job
You will be responsible for quality assurance of Novo Nordisk supply chain processes with focus on Master Data. You will head up a Master Data Quality network consisting of process experts across Novo Nordisk and will take part of a master data advisory board, setting direction for the way Novo Nordisk work with master data. You will work closely with our colleagues in Digital Supply Chain, an area in our Line of Business, and with international stakeholders both within and outside Novo Nordisk and you should expect a high level of complexity in your daily tasks. Beside this you and your collages in SC QA are responsible for ensuring compliance, product quality and patient safety in SC QA’s daily operations and have to offer QA support and GMP guidance internally to Supply Chain Planning & Logistic (SAP, planning processes and handling of master data among other). Your tasks will be to review and approve quality related documents such as SOP’s, deviations, and change control cases, participate, and set quality direction for major projects, and you will also participate in relevant audits and inspections. Qualifications You hold a M.Sc. in pharmacy, engineering, IT or equivalent, You have at least 3-5 years of work experience related to quality assurance in the pharmaceutical industry, preferably within supply chain and Master Data. You are skilled within interpretation and application of quality requirements. As a person, you: Are known for your positive mindset, flexibility, and persistence. You take responsibility for your assignments, and you are solution oriented and exhibit a pragmatic attitude when solving complex issues leading you to find constructive solutions. You can take leadership in projects, and secure implementation of agreed solutions and thereby can develop our internal processes and affect the way we work with our stakeholders both internally and externally. Quality mindset is an integrated part of your personality, and you can balance compliance and product quality when making decisions and can stay firm when needed to secure the quality and compliance aspects. As you will work in an international organisation with many internal and external stakeholders you must have excellent communication, collaboration, and presentation skills and you will need to be proficient in English both in speaking and writing.
Contact For further information, please contact QA Director Cecilie Weiersøe Højer at +45 3075 7005. Deadline February 28th, 2024 Please notice that interviews are held on an ongoing basis. Working at Novo Nordisk 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. 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.
About the department
Supply Chain QA is responsible for Quality Assurance and support of Supply Chain Planning and Logistic activities including cold chain distribution of Novo Nordisk products worldwide, production planning across the entire Novo Nordisk supply chain, and data management and governance across Novo Nordisk. The department has 18 employees and is expected to grow in the coming years.
In our daily work we work closely together with Supply Chain Planning & Logistic (SCP&L) – our Line of Business, whom we support in quality matters, are involved in high impact projects, and set quality direction for. You will become part of a team focusing on the digital part of our supply chain incl. master data and planning processes. It is a team which have a high level of self-governance, good working relations, are informal and value professional sparring and good humour highly.
The job
You will be responsible for quality assurance of Novo Nordisk supply chain processes with focus on Master Data. You will head up a Master Data Quality network consisting of process experts across Novo Nordisk and will take part of a master data advisory board, setting direction for the way Novo Nordisk work with master data. You will work closely with our colleagues in Digital Supply Chain, an area in our Line of Business, and with international stakeholders both within and outside Novo Nordisk and you should expect a high level of complexity in your daily tasks. Beside this you and your collages in SC QA are responsible for ensuring compliance, product quality and patient safety in SC QA’s daily operations and have to offer QA support and GMP guidance internally to Supply Chain Planning & Logistic (SAP, planning processes and handling of master data among other). Your tasks will be to review and approve quality related documents such as SOP’s, deviations, and change control cases, participate, and set quality direction for major projects, and you will also participate in relevant audits and inspections. Qualifications
Contact For further information, please contact QA Director Cecilie Weiersøe Højer at +45 3075 7005. Deadline February 28th, 2024 Please notice that interviews are held on an ongoing basis. Working at Novo Nordisk 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. 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 Bagsværd.
Jobbet er oprettet på vores service den 25.1.2024, 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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