Lead Auditor
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Do you have what it takes to initiate, prepare and conduct audits of suppliers to Novo Nordisk and report on them effectively? Are you excited about the opportunity to impact digitalization processes and support your colleagues in this area? Do you want to be a part of knowledge sharing and implementing standards across the company while opening up new development opportunities and career paths for your future?
Then you can be part of a life-changing career in Novo Nordisk Supplier Audits, read more and apply now!
The position
As our new Lead Auditor, you will join our Supplier Audits department and be responsible for auditing Novo Nordisk suppliers world-wide.
Your daily tasks will focus on:
• Initiating and preparing the audits in close collaboration with stakeholders
• Conducting and reporting on routine-, for cause-, and qualification audits
• Sharing up-to-date knowledge of external requirements and best practices with peers and internal stakeholders
• Identifying and reporting compliance trends and signals
• Acting as subject matter expert in own business area by making recommendations and setting directions.
Moreover, you will have the opportunity to demonstrate personal impact through your competencies and knowledge deployed critically to the core processes in your own business area, the anticipation of opportunities and threats, and adjustment of own objectives.
Your impact will also extend to digitalization processes as well as lead and support your colleagues in this area.
As Lead Auditor you will get to see many Novo Nordisk suppliers and be part of knowledge sharing and setting standards across the company. The position will as well open new development opportunities, as well as new career paths for the future.
Qualifications
To succeed in this role, you:
• Hold a master’s degree within a relevant field
• Have several years of experience in the pharmaceutical industry either as an auditor or in QA roles
• Have solid knowledge and experience within GMP and ISO
• Have extensive knowledge of the potential risk of key processes and relevant regulatory requirements
• Are fluent in English, both written and spoken We will also positively evaluate good IT skills and understanding of digitalization processes. On a personal level, you possess strong stakeholder and collaboration skills in a multinational context, other than the ability to identify risk areas, keep time and conclude while being flexible and adaptable to change. Finally, you should be open to travel internationally, as you will be conducting audits for international suppliers.
About the department
Supplier Audits is a part of Novo Nordisk Quality Audits & Inspections and delivers value by conducting independent, objective and risk-based supplier audits, escalating signals, trends, and recommendations to senior management and seizing opportunities to maximize value creation for Novo Nordisk using the unique role and expertise of quality auditors.
Our mission is to provide executive management with assurance of the highest quality for patients, to ensure product quality and compliance, and to drive improvements and simplicity for Novo Nordisk.
We employ 20 highly specialized auditors and we are one of four departments in the Quality Audits & Inspections area, which has 90+ employees in Denmark, India, US, Israel, UK, Canada and China. Quality Audits & inspections conduct more than 700 audits annually and have process responsibility for the audits conducted globally within GMP, ISO, GCP, GDP, PV and GLP. Quality Audits & Inspections offers an engaging work environment, with collaboration across the organization and people with many different backgrounds. 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
For further information, please contact Saso Kotevski at +45 3079 1868 or Lars Mortensen at +45 3079 9809.
Deadline
29 October 2023 Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is 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.
Then you can be part of a life-changing career in Novo Nordisk Supplier Audits, read more and apply now!
The position
As our new Lead Auditor, you will join our Supplier Audits department and be responsible for auditing Novo Nordisk suppliers world-wide.
Your daily tasks will focus on:
• Initiating and preparing the audits in close collaboration with stakeholders
• Conducting and reporting on routine-, for cause-, and qualification audits
• Sharing up-to-date knowledge of external requirements and best practices with peers and internal stakeholders
• Identifying and reporting compliance trends and signals
• Acting as subject matter expert in own business area by making recommendations and setting directions.
Moreover, you will have the opportunity to demonstrate personal impact through your competencies and knowledge deployed critically to the core processes in your own business area, the anticipation of opportunities and threats, and adjustment of own objectives.
Your impact will also extend to digitalization processes as well as lead and support your colleagues in this area.
As Lead Auditor you will get to see many Novo Nordisk suppliers and be part of knowledge sharing and setting standards across the company. The position will as well open new development opportunities, as well as new career paths for the future.
Qualifications
To succeed in this role, you:
• Hold a master’s degree within a relevant field
• Have several years of experience in the pharmaceutical industry either as an auditor or in QA roles
• Have solid knowledge and experience within GMP and ISO
• Have extensive knowledge of the potential risk of key processes and relevant regulatory requirements
• Are fluent in English, both written and spoken We will also positively evaluate good IT skills and understanding of digitalization processes. On a personal level, you possess strong stakeholder and collaboration skills in a multinational context, other than the ability to identify risk areas, keep time and conclude while being flexible and adaptable to change. Finally, you should be open to travel internationally, as you will be conducting audits for international suppliers.
About the department
Supplier Audits is a part of Novo Nordisk Quality Audits & Inspections and delivers value by conducting independent, objective and risk-based supplier audits, escalating signals, trends, and recommendations to senior management and seizing opportunities to maximize value creation for Novo Nordisk using the unique role and expertise of quality auditors.
Our mission is to provide executive management with assurance of the highest quality for patients, to ensure product quality and compliance, and to drive improvements and simplicity for Novo Nordisk.
We employ 20 highly specialized auditors and we are one of four departments in the Quality Audits & Inspections area, which has 90+ employees in Denmark, India, US, Israel, UK, Canada and China. Quality Audits & inspections conduct more than 700 audits annually and have process responsibility for the audits conducted globally within GMP, ISO, GCP, GDP, PV and GLP. Quality Audits & Inspections offers an engaging work environment, with collaboration across the organization and people with many different backgrounds. 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
For further information, please contact Saso Kotevski at +45 3079 1868 or Lars Mortensen at +45 3079 9809.
Deadline
29 October 2023 Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is 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 Bagsværd.
Jobbet er oprettet på vores service den 10.10.2023, 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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