QA IT Specialist
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Do you want to use your IT and quality skills to make good decisions and set direction in IT projects across our global organisation in chemistry manufacturing and controls (CMC) and CMC Quality Assurance (CMC QA)? Are you always looking for improvements and keep challenging the status quo within IT? If so, this position as CMC QA IT Specialist can be a unique opportunity for you.
The position As our CMC QA IT Specialist, you will be one point of contact between Quality IT (NNQ IT), Digital Data & IT(DD&IT) and local CMC QA for cross-organisational IT solutions. You will be the channel for local QA to challenge global IT solutions and the link for escalating local perspectives to the global organisation. Part of the job is to ensure efficient and effective implementation of global IT solutions and optimisations, alignment with local processes to the global approach. You will be empowered to make decisions on behalf of CMC QA, work closely with CMC QA MGMT on the IT strategy, and use your skills to create followership in the organisation. In the role, you will support and equip local CMC QA to make robust quality decisions and increase the IT confidence levels in QA. Your responsibility Be one point of entry between NNQ IT / DD & IT and CMC QA Utilize own expert knowledge on complex IT QA related challenges across CMC and CMC QA Influence the quality and compliance strategy and agenda on CMC and corporate levels Spearhead CMC QA IT group across our departments and be responsible for the development and training of the group System Owner of our local QA IT system for Clinical Trials applications Use your good leadership skills and ability to create followship in our organisation Have a good understanding for processes and quality requirements Set direction, drive projects, and deliver results in an environment that fosters innovation and creative thinking Qualifications
To succeed in this role, you have: A master’s degree or PhD within IT, pharmacy, engineering, or other related fields At least 5 years of experience from the pharmaceutical industry within IT project management, quality, or production A flair for stakeholder management and networking at various organisational levels Strong communication skills, with proficiency in English; understanding Danish is an advantage In-depth understanding of IT compliance requirements As a person, you are ambitious, proactive, and curious. You never lose focus, despite changing demands. You share a positive energy and can see the unreleased potential in new ideas. Most importantly you have a passion for IT and Compliance to ensure the highest quality to our patients. About the department
Our CVP area are located across sites around greater Copenhagen area and in the US. We consist of around 175 dedicated and highly talented employees. Our main purpose is to safeguard patient safety and ensure product quality and compliance in the CMC area, and ultimately release drug candidates for clinical trials. As part of Quality, we support the business and strive for simplicity every single day, to ensure Novo Nordisk’s critical delivery of medicine to patients.
You will be part of a strong culture, where we strive for high psychological safety, give regular feedback, and understand that the most important thing we have is our people. Working at
At , we always strive for excellence and continuously develop our expertise to stay ahead - both as a company and as individuals. We believe that innovation and creativity thrive in a healthy and engaging working environment. Therefore, we give you the opportunity to bring your personal ambition and passion to work to improve the quality of life of the patients. Contact
For further information, please contact QA Director Casper Yding +.
Deadline
5 April 2024. Note that applications will be reviewed on an ongoing basis and the position will be closed when we find the right candidate.
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 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 our CMC QA IT Specialist, you will be one point of contact between Quality IT (NNQ IT), Digital Data & IT(DD&IT) and local CMC QA for cross-organisational IT solutions. You will be the channel for local QA to challenge global IT solutions and the link for escalating local perspectives to the global organisation. Part of the job is to ensure efficient and effective implementation of global IT solutions and optimisations, alignment with local processes to the global approach. You will be empowered to make decisions on behalf of CMC QA, work closely with CMC QA MGMT on the IT strategy, and use your skills to create followership in the organisation. In the role, you will support and equip local CMC QA to make robust quality decisions and increase the IT confidence levels in QA. Your responsibility
To succeed in this role, you have:
Our CVP area are located across sites around greater Copenhagen area and in the US. We consist of around 175 dedicated and highly talented employees. Our main purpose is to safeguard patient safety and ensure product quality and compliance in the CMC area, and ultimately release drug candidates for clinical trials. As part of Quality, we support the business and strive for simplicity every single day, to ensure Novo Nordisk’s critical delivery of medicine to patients.
You will be part of a strong culture, where we strive for high psychological safety, give regular feedback, and understand that the most important thing we have is our people. Working at
At , we always strive for excellence and continuously develop our expertise to stay ahead - both as a company and as individuals. We believe that innovation and creativity thrive in a healthy and engaging working environment. Therefore, we give you the opportunity to bring your personal ambition and passion to work to improve the quality of life of the patients. Contact
For further information, please contact QA Director Casper Yding +.
Deadline
5 April 2024. Note that applications will be reviewed on an ongoing basis and the position will be closed when we find the right candidate.
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 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 Måløv.
Jobbet er oprettet på vores service den 19.3.2024, 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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