QA Professional
- Quality
- Denmark - Måløv
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 department of 20 colleagues located in Måløv. We are part of the CMC Quality Assurance organisation, 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
The organisation’s continuing high level of compliance, audit and inspection readiness is on top of your agenda.
As a Qualified Persons delegate you will certify final packed products for use in clinical trials worldwide. You will be responsible for quality assurance of activities and documents related to labelling, packaging and supplying products for Novo Nordisk trials globally. You will review and approve procedures, change requests and cases of non-conformities and customer complaints.
You will provide quality support where your ability to apply Novo Nordisk and authority regulations and requirements is key to solving challenges in both daily operation and long term development of the business and its quality system. You will interact with colleagues across the CMC Supply organisation and also with colleagues from other parts of Novo Nordisk A/S both in Denmark but also with affiliates worldwide.
You can look forward to entering into an energetic and positive working environment where cooperation amongst highly engaged and dedicated Novo Nordisk colleagues is key to your and the company’s success.
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 (§39). Direct experience with GMP work related to clinical trials should be highlighted in your application as this will be weighted highly when evaluating applicants.
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 organisational levels. You like a professional and dynamic environment with many simultaneous tasks and changing priorities.
You are 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 help 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
19 January 2014.
- Quality
- Denmark - Måløv
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 department of 20 colleagues located in Måløv. We are part of the CMC Quality Assurance organisation, 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
The organisation’s continuing high level of compliance, audit and inspection readiness is on top of your agenda.
As a Qualified Persons delegate you will certify final packed products for use in clinical trials worldwide. You will be responsible for quality assurance of activities and documents related to labelling, packaging and supplying products for Novo Nordisk trials globally. You will review and approve procedures, change requests and cases of non-conformities and customer complaints.
You will provide quality support where your ability to apply Novo Nordisk and authority regulations and requirements is key to solving challenges in both daily operation and long term development of the business and its quality system. You will interact with colleagues across the CMC Supply organisation and also with colleagues from other parts of Novo Nordisk A/S both in Denmark but also with affiliates worldwide.
You can look forward to entering into an energetic and positive working environment where cooperation amongst highly engaged and dedicated Novo Nordisk colleagues is key to your and the company’s success.
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 (§39). Direct experience with GMP work related to clinical trials should be highlighted in your application as this will be weighted highly when evaluating applicants.
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 organisational levels. You like a professional and dynamic environment with many simultaneous tasks and changing priorities.
You are 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 help 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
19 January 2014.