QA Professional
- Quality
- Denmark - Måløv
Do you have a mind for Quality Assurance? Do you see yourself contributing to high quality and compliance of products used for Novo Nordisk clinical trials globally?
About the department
You will be part of a dedicated team of 19 colleague located in Måløv. We are part of CMC Quality Assurance organization, which is responsible for all QA activities related to Investigational Medicinal Products used for the increasing number of Novo Nordisk clinical trials globally. We are looking for a new colleague to support the quality activities in the clinical supplies part of the Novo Nordisk R&D organisation.
The job
You will, as a delegated Qualified Person, be responsible for status assignment of products for Novo Nordisk clinical trials. The organisations continuing high level of compliance, audit and inspection readiness is on top of your agenda. You contribute to finding the right balance between patient safety, compliance to requirements and effective business conduct. You represent the department in quality issues where the ability to apply Novo Nordisk and authority regulations and requirements is key to support solving challenges in both daily operation and long term development of the business. As the department does have relations across the organisation to areas that work according to GCP regulations you will be involved in issues that relate directly to the conduct of the trials across the world. On an operational level you will also be responsible for quality assurance of activities and documents related to the labeling, packaging and supplying of IMP for Novo Nordisk trials globally. You review and approve procedures, requests for changes, processes and cases of non-conformities and customer complaints. You can look forward to entering into an energetic and positive working environment where cooperation amongst engaged and dedicated Novo Nordisk colleague is a keyword.
Qualifications
Your approach to this position is a master’s degree as a Pharmacist. The preferred candidate has a minimum of 3-4 years experience working according to GMP requirements (production/QA) in a pharmaceutical business with a manufacturing authorization from DHMA. On a personal level, you demonstrate engagement, credibility and empowerment. You are a positive and open minded team player who can co-operate at all organizational levels. You like a professional and dynamic environment with many simultaneous tasks and changing priorities. You are a team player and a skilled communicator, and you thrive on unfolding your high level of energy and spirit in an international, dynamic environment.
Feel free to submit your job application in either English or Danish, whichever you prefer. Also please share this add with friends and professional connections you might think would be interested in pursuing a career opportunity at Novo Nordisk.
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information please contact Birthe Boldvig Rottwitt at +45 3075 0158.
Deadline
20 September 2013.
- Quality
- Denmark - Måløv
Do you have a mind for Quality Assurance? Do you see yourself contributing to high quality and compliance of products used for Novo Nordisk clinical trials globally?
About the department
You will be part of a dedicated team of 19 colleague located in Måløv. We are part of CMC Quality Assurance organization, which is responsible for all QA activities related to Investigational Medicinal Products used for the increasing number of Novo Nordisk clinical trials globally. We are looking for a new colleague to support the quality activities in the clinical supplies part of the Novo Nordisk R&D organisation.
The job
You will, as a delegated Qualified Person, be responsible for status assignment of products for Novo Nordisk clinical trials. The organisations continuing high level of compliance, audit and inspection readiness is on top of your agenda. You contribute to finding the right balance between patient safety, compliance to requirements and effective business conduct. You represent the department in quality issues where the ability to apply Novo Nordisk and authority regulations and requirements is key to support solving challenges in both daily operation and long term development of the business. As the department does have relations across the organisation to areas that work according to GCP regulations you will be involved in issues that relate directly to the conduct of the trials across the world. On an operational level you will also be responsible for quality assurance of activities and documents related to the labeling, packaging and supplying of IMP for Novo Nordisk trials globally. You review and approve procedures, requests for changes, processes and cases of non-conformities and customer complaints. You can look forward to entering into an energetic and positive working environment where cooperation amongst engaged and dedicated Novo Nordisk colleague is a keyword.
Qualifications
Your approach to this position is a master’s degree as a Pharmacist. The preferred candidate has a minimum of 3-4 years experience working according to GMP requirements (production/QA) in a pharmaceutical business with a manufacturing authorization from DHMA. On a personal level, you demonstrate engagement, credibility and empowerment. You are a positive and open minded team player who can co-operate at all organizational levels. You like a professional and dynamic environment with many simultaneous tasks and changing priorities. You are a team player and a skilled communicator, and you thrive on unfolding your high level of energy and spirit in an international, dynamic environment.
Feel free to submit your job application in either English or Danish, whichever you prefer. Also please share this add with friends and professional connections you might think would be interested in pursuing a career opportunity at Novo Nordisk.
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information please contact Birthe Boldvig Rottwitt at +45 3075 0158.
Deadline
20 September 2013.