Process and Compliance Expert
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Søborg
Do you want to be part of transforming the way Regulatory Affairs operates ensuring compliant and efficient processes in a global pharma company? This role is an excellent opportunity to make a significant impact on product quality, patient safety, regulatory compliance and business performance and shape the future of Regulatory Affairs. We are searching for a person who is motivated by looking for opportunities for improvement and drive changes. In this role you will get a Regulatory Affairs network to collaborate with you in challenges like process digitalisation to support compliant and efficient processes. The Position
Together with our Process Managers you will be responsible for a dedicated area ensuring compliance and continuous optimisation of the labelling processes. The role will develop over time along with the department and area. The main responsibilities will include: Use data insights to identify optimisation opportunities, bottlenecks and facilitate decisions Engage with stakeholders, provide process guidance and regulatory input to ensure fit for purpose processes and solutions Develop new ways of working that impact processes and solutions while ensuring compliance and business value Ensure alignment with external regulatory requirements Be responsible for the onboarding programs for new employees within Regulatory Affairs Drive audit/inspection readiness activities Qualifications
We believe in building a culture of individual accountability and ownership and need people that can embrace that mentality. The ideal candidate should have: A bachelor’s and / or master’s degree in a relevant field, such as science, pharmacy, engineering or equivalent At least, 5 years of experience working in a GxP regulated environment, such as food, oil and gas, medical devices, financial services; pharmaceutical industry experience is a plus Demonstrated experience working with business processes improvement, and compliance Strong compliance, and quality mindset Fluency in English both written and spoken As a person, you are curious to learn, well organised, and a proactive problem solver, enjoying working in a diverse and global team and good at communicating complex ideas clearly, effectively and with impact to enable business decisions.
About the Department
Regulatory Affairs is an exciting area involved across the full value chain. We are responsible for global regulatory strategies to obtain and maintain regulatory licenses for current and future products, responsive to the worldwide business needs of Novo Nordisk. In this role, you will be part of a strategically crucial business transformation program and take active part in shaping the way Regulatory Affairs will work in the future. You will join the new department RA Business Compliance that plays a key role in supporting and enabling this transformation. The department consists of Process Experts, Business Analysts and Data Analysts located in Denmark and India. In this position you will be based with our team in Søborg, Denmark. The atmosphere in the department is informal and our commitment to innovation also applies to the way we work. We embrace a flexible workplace, with a blend of in-office and remote work. Working At Novo Nordisk
At Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases. By combining our innovation and commercial excellence, we draw upon insights from patients and partners to transform bold ideas into life-saving and preventive medicines. Our ambition is to take the lead in each of these areas, driving change with an unfailing belief that it can be done. Contact
For further information, please contact Fredrik Wikström at +45 3079 2317 or [email protected]. Deadline
23 June 2024. You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Please assist us in maintaining a fair and inclusive selection process by not attaching a photo to your application. 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.
Together with our Process Managers you will be responsible for a dedicated area ensuring compliance and continuous optimisation of the labelling processes. The role will develop over time along with the department and area. The main responsibilities will include:
We believe in building a culture of individual accountability and ownership and need people that can embrace that mentality. The ideal candidate should have:
About the Department
Regulatory Affairs is an exciting area involved across the full value chain. We are responsible for global regulatory strategies to obtain and maintain regulatory licenses for current and future products, responsive to the worldwide business needs of Novo Nordisk. In this role, you will be part of a strategically crucial business transformation program and take active part in shaping the way Regulatory Affairs will work in the future. You will join the new department RA Business Compliance that plays a key role in supporting and enabling this transformation. The department consists of Process Experts, Business Analysts and Data Analysts located in Denmark and India. In this position you will be based with our team in Søborg, Denmark. The atmosphere in the department is informal and our commitment to innovation also applies to the way we work. We embrace a flexible workplace, with a blend of in-office and remote work. Working At Novo Nordisk
At Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases. By combining our innovation and commercial excellence, we draw upon insights from patients and partners to transform bold ideas into life-saving and preventive medicines. Our ambition is to take the lead in each of these areas, driving change with an unfailing belief that it can be done. Contact
For further information, please contact Fredrik Wikström at +45 3079 2317 or [email protected]. Deadline
23 June 2024. You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Please assist us in maintaining a fair and inclusive selection process by not attaching a photo to your application. 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 "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 8.3.2024, 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.
- Apoteker
- Søborg
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