Senior QA Process Manager
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Gentofte
Would you like to play a pivotal role in implementing our Data Integrity and becoming a part of exciting journey? Are you eager to contribute to our data integrity vision, sharing best practices through effective collaboration? If yes, then this might be the right opportunity for you. Read more below and apply today! The position
This role requires a dynamic individual who can establish robust process groups, providing essential support to Data Owners, Data Integrity Stewards, and QAs. You will share your insight in planning, data mapping, and performing risk assessments, which will lead to strong mitigating actions that strengthen our availability of high-integrity data. Your main responsibilities will also include:
•Guiding the process group members in the practice of data integrity governance, audit trail requirements, data mapping, and risk assessments
•Facilitating the identification of potential risks and formulating effective mitigating actions to ensure optimal data integrity
•Cultivating a culture of continuous process improvement and promoting best practices in data management and audit trail requirements
•Advising and training relevant stakeholders on Data Integrity-related topics
•Reviewing and updating training materials related to Data Integrity
•Participating in the Records Management Corporate Process Group by sharing insights and best practices
Qualifications
We envision that you have a robust background in developing and maintaining quality processes within the pharmaceutical or medical device industry. Additionally, you have demonstrated prowess as a strong partner and advisor in quality-related issues. To excel in this role, you:
•Hold a master’s degree in life sciences or other relevant field
•Have strong experience in Quality Assurance within Pharmaceuticals or Medical Devices
•Have experience in data governance and data integrity
•Possess strong experience in project and stakeholder management
•Are fluent in English About the department
The Biotech & Rare Diseases QA area has 275 employees, organized across six departments. Five of these departments are in Denmark and one in the US. You will have the opportunity to join our cross-functional QA Business Support Team, which includes our most experienced QA professionals, project managers, and specialists. The team has a high level of self-governance, and our working relationships are informal. We appreciate a colleague who takes responsibility, has a positive and curious approach to new challenges, and contributes to a great working atmosphere, as we are convinced that this is the key to creating strong results. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
If you want to know more about the position, please contact Associate Manager, Søren Tomra at +45 34 48 88 42 Deadline
9 January 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified.
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 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.
This role requires a dynamic individual who can establish robust process groups, providing essential support to Data Owners, Data Integrity Stewards, and QAs. You will share your insight in planning, data mapping, and performing risk assessments, which will lead to strong mitigating actions that strengthen our availability of high-integrity data. Your main responsibilities will also include:
•Guiding the process group members in the practice of data integrity governance, audit trail requirements, data mapping, and risk assessments
•Facilitating the identification of potential risks and formulating effective mitigating actions to ensure optimal data integrity
•Cultivating a culture of continuous process improvement and promoting best practices in data management and audit trail requirements
•Advising and training relevant stakeholders on Data Integrity-related topics
•Reviewing and updating training materials related to Data Integrity
•Participating in the Records Management Corporate Process Group by sharing insights and best practices
Qualifications
We envision that you have a robust background in developing and maintaining quality processes within the pharmaceutical or medical device industry. Additionally, you have demonstrated prowess as a strong partner and advisor in quality-related issues. To excel in this role, you:
•Hold a master’s degree in life sciences or other relevant field
•Have strong experience in Quality Assurance within Pharmaceuticals or Medical Devices
•Have experience in data governance and data integrity
•Possess strong experience in project and stakeholder management
•Are fluent in English About the department
The Biotech & Rare Diseases QA area has 275 employees, organized across six departments. Five of these departments are in Denmark and one in the US. You will have the opportunity to join our cross-functional QA Business Support Team, which includes our most experienced QA professionals, project managers, and specialists. The team has a high level of self-governance, and our working relationships are informal. We appreciate a colleague who takes responsibility, has a positive and curious approach to new challenges, and contributes to a great working atmosphere, as we are convinced that this is the key to creating strong results. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
If you want to know more about the position, please contact Associate Manager, Søren Tomra at +45 34 48 88 42 Deadline
9 January 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified.
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 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 Gentofte.
Jobbet er oprettet på vores service den 8.12.2023, 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.
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