Biopharm QA internal auditor
- Quality
- Denmark - Gentofte
Would you like to go on a compliance mission? And are GMP and auditing your areas of interest? Then we have the right job for you as QMS professional. Here is the opportunity for a career with good possibilities of development, a dynamic work day and many contacts across the entire Biopharm.
About the department
In Biopharm QA Support we have the overall responsibility for quality assurance tasks across the organisation – from inspections to QA/GMP training to quality KPI reporting. Furthermore we have the responsibility for Biopharm MDev and Biopharm Business Support.We are 6 employees and 1 department manager.
About the job
You will play an important role in our organisation, as you will be part of the first Biopharm internal audit teamYou will be responsible for implementing internal auditing function in Biopharm which should ensure a regular check of the level of compliance in the organisation and secure inspection readiness. This will be achieved by performing systematic spot checks on main GMP documents and production activities. The checks can be performed both from your desk and in the departments.As QMS professional, you will interact with all the functions in the Biopharm organisation and your knowledge on GMP should be broad to cover all the areas in Biopharm (from API to FP, from tablets to biotech products).The position is new and therefore you have the chance to shape your job
Qualifications
You hold a masters degree within natural sciences, e.g. pharmacist, engineer, chemist etc. Furthermore, you have a strong quality mind-set and a high degree of responsibility. You have a minimum of 3-4 years of practical experience with GMP and QA and it will be an advantage if you have practical experience leading audits and a hence you have a structured approach to planning and carrying out activities.You are able to cooperate and communicate with all types of colleagues and other stakeholders. You are able to prioritise your time and to manage several tasks at the same time.
On a personal level, we expect you to be outgoing, trustworthy and able to communicate your messages clearly. You have a balanced robust personality and enjoy the high activity of the QA work across functions, processes and products.Fluency in written and spoken Danish is required as well as English.You are welcome to apply for this position either in Danish or in English.
Learn more about Novo Nordisk ProductSupply and working in QA using this link www.novonordisk.com/careers/QA.
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 Cristina De Simoni Klitgaard on +45 3075 6783.
Deadline
12 August 2013.
- Quality
- Denmark - Gentofte
Would you like to go on a compliance mission? And are GMP and auditing your areas of interest? Then we have the right job for you as QMS professional. Here is the opportunity for a career with good possibilities of development, a dynamic work day and many contacts across the entire Biopharm.
About the department
In Biopharm QA Support we have the overall responsibility for quality assurance tasks across the organisation – from inspections to QA/GMP training to quality KPI reporting. Furthermore we have the responsibility for Biopharm MDev and Biopharm Business Support.We are 6 employees and 1 department manager.
About the job
You will play an important role in our organisation, as you will be part of the first Biopharm internal audit teamYou will be responsible for implementing internal auditing function in Biopharm which should ensure a regular check of the level of compliance in the organisation and secure inspection readiness. This will be achieved by performing systematic spot checks on main GMP documents and production activities. The checks can be performed both from your desk and in the departments.As QMS professional, you will interact with all the functions in the Biopharm organisation and your knowledge on GMP should be broad to cover all the areas in Biopharm (from API to FP, from tablets to biotech products).The position is new and therefore you have the chance to shape your job
Qualifications
You hold a masters degree within natural sciences, e.g. pharmacist, engineer, chemist etc. Furthermore, you have a strong quality mind-set and a high degree of responsibility. You have a minimum of 3-4 years of practical experience with GMP and QA and it will be an advantage if you have practical experience leading audits and a hence you have a structured approach to planning and carrying out activities.You are able to cooperate and communicate with all types of colleagues and other stakeholders. You are able to prioritise your time and to manage several tasks at the same time.
On a personal level, we expect you to be outgoing, trustworthy and able to communicate your messages clearly. You have a balanced robust personality and enjoy the high activity of the QA work across functions, processes and products.Fluency in written and spoken Danish is required as well as English.You are welcome to apply for this position either in Danish or in English.
Learn more about Novo Nordisk ProductSupply and working in QA using this link www.novonordisk.com/careers/QA.
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 Cristina De Simoni Klitgaard on +45 3075 6783.
Deadline
12 August 2013.