GCP Lead Auditor
- Quality
- Denmark - Bagsværd
Do you want to be part of one of the world’s most successful pharmaceutical companies? Do you have a dream of a job with a high level of responsibility and interaction with many different cultures? Do you have a strong quality mindset and solid experience within GCP? Then you may be one of our four new GCP lead auditors.
About the department
As a GCP lead auditor, you will be part of GCP Audits. The department is located in Bagsværd at the Head Quarter in Denmark and has global responsibility for performing audits of clinical trials throughout all development phases. Due to increased activities we will expand with four new GCP lead auditor positions.
The job
We share audit experiences and GCP issues in the department, and work together to develop a consistent auditing approach at a high professional level. The job is characterized by a high level of responsibility and interaction with many different types of people at all levels of the organization across many different cultures. As GCP lead auditor you will perform audits of clinical trials and related quality systems worldwide. Novo Nordisk sponsors clinical trials in 70+ countries, and you should expect approximately 80 annual travel days outside Denmark. You will communicate and interact with management, auditors and employees at all organisational levels within Novo Nordisk and at CROs. Your audits will help to ensure ethical conduct, safety of subjects, and validity and quality of data. Through audits, you will have a significant influence on maintaining and implementing internal procedures and on continuous improvement of the Novo Nordisk quality system.
Qualifications
You hold a university degree in pharmaceutical or natural science or a related discipline. In addition, you have clinical development and/or quality assurance experience. You have up-to-date knowledge of relevant GCP requirements and the ability to interpret applicable standards and make objective decisions. You are a committed and open-minded person who likes to be in daily contact with different cultures and colleagues around the world. In addition, you have excellent communication skills and high cultural awareness in order to interact with many different stakeholders and manage conflicts in a constructive way. You thrive in a busy environment with changing priorities. Since most of the audits are conducted outside Denmark, you must be fluent in English both orally and in writing.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Bilal Ghazal at +45 4443 3122.
Deadline
27 January 2014.
- Quality
- Denmark - Bagsværd
Do you want to be part of one of the world’s most successful pharmaceutical companies? Do you have a dream of a job with a high level of responsibility and interaction with many different cultures? Do you have a strong quality mindset and solid experience within GCP? Then you may be one of our four new GCP lead auditors.
About the department
As a GCP lead auditor, you will be part of GCP Audits. The department is located in Bagsværd at the Head Quarter in Denmark and has global responsibility for performing audits of clinical trials throughout all development phases. Due to increased activities we will expand with four new GCP lead auditor positions.
The job
We share audit experiences and GCP issues in the department, and work together to develop a consistent auditing approach at a high professional level. The job is characterized by a high level of responsibility and interaction with many different types of people at all levels of the organization across many different cultures. As GCP lead auditor you will perform audits of clinical trials and related quality systems worldwide. Novo Nordisk sponsors clinical trials in 70+ countries, and you should expect approximately 80 annual travel days outside Denmark. You will communicate and interact with management, auditors and employees at all organisational levels within Novo Nordisk and at CROs. Your audits will help to ensure ethical conduct, safety of subjects, and validity and quality of data. Through audits, you will have a significant influence on maintaining and implementing internal procedures and on continuous improvement of the Novo Nordisk quality system.
Qualifications
You hold a university degree in pharmaceutical or natural science or a related discipline. In addition, you have clinical development and/or quality assurance experience. You have up-to-date knowledge of relevant GCP requirements and the ability to interpret applicable standards and make objective decisions. You are a committed and open-minded person who likes to be in daily contact with different cultures and colleagues around the world. In addition, you have excellent communication skills and high cultural awareness in order to interact with many different stakeholders and manage conflicts in a constructive way. You thrive in a busy environment with changing priorities. Since most of the audits are conducted outside Denmark, you must be fluent in English both orally and in writing.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Bilal Ghazal at +45 4443 3122.
Deadline
27 January 2014.