Senior QMS professional
- Research & Development
- Denmark - Søborg
Would you enjoy working with Quality Management System (QMS) in the Research & Development area in a large company? Can you with an open minded attitude argue for adhering to the requirements covering QMS, GCP and ISO9001 internally as well as externally? If you find challenges like this exciting and inspiring, you may be our new Senior QMS Professional with focus on QMS.
About the department
The QA R&D department, a part of Quality R&D in Global Development, is looking for a replacement for our competent Senior QMS Professional.
QA R&D works with quality activities including QA responsibilities across R&D units, and has responsibilities within maintenance of QMS and quality improvement activities. The department is split into teams and is organised with professional Team Coordinators in each team and visible leadership characterises the department.
The Job
The position is placed in the QMS team focusing on processes in R&D locally as well as globally. The main responsibility as Senior QMS Professional is to have an academic focus on continuous maintenance and improvement of quality. This includes participation and planning of audits, quality training, support to stakeholders and management of minor quality projects. Review of documents and QA approval of quality records is also an important part of the job. You will take an active role as the QA and QMS Advisor in R&D globally and travel will to a limited extent be a part of the job. Our stakeholders’ primary regulatory requirements are QMS, GCP and ISO9001. You will cooperate with other types of professionals and international cultures, and personal flexibility is a must. Together with the team and the stakeholders, you will be able to influence the quality mind-set within R&D at Novo Nordisk.
Qualifications
You hold a scientific academic degree or equivalent and have a strong command of written and spoken English on a professional level. It is an advantage if you have been in a pharmaceutical company before and have worked with QMS, GCP, ISO9001 and QA.
You have robust and strong interpersonal skills. You must be detail-oriented with a strong quality mind-set, but take a pragmatic approach to problem solving. You are a team player who thrives with working across departments in an international organisation.
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 Pia Sandau on+45 3075 8334 or Lone Bau on +45 3075 7225.
Deadline
4 August 2013.
- Research & Development
- Denmark - Søborg
Would you enjoy working with Quality Management System (QMS) in the Research & Development area in a large company? Can you with an open minded attitude argue for adhering to the requirements covering QMS, GCP and ISO9001 internally as well as externally? If you find challenges like this exciting and inspiring, you may be our new Senior QMS Professional with focus on QMS.
About the department
The QA R&D department, a part of Quality R&D in Global Development, is looking for a replacement for our competent Senior QMS Professional.
QA R&D works with quality activities including QA responsibilities across R&D units, and has responsibilities within maintenance of QMS and quality improvement activities. The department is split into teams and is organised with professional Team Coordinators in each team and visible leadership characterises the department.
The Job
The position is placed in the QMS team focusing on processes in R&D locally as well as globally. The main responsibility as Senior QMS Professional is to have an academic focus on continuous maintenance and improvement of quality. This includes participation and planning of audits, quality training, support to stakeholders and management of minor quality projects. Review of documents and QA approval of quality records is also an important part of the job. You will take an active role as the QA and QMS Advisor in R&D globally and travel will to a limited extent be a part of the job. Our stakeholders’ primary regulatory requirements are QMS, GCP and ISO9001. You will cooperate with other types of professionals and international cultures, and personal flexibility is a must. Together with the team and the stakeholders, you will be able to influence the quality mind-set within R&D at Novo Nordisk.
Qualifications
You hold a scientific academic degree or equivalent and have a strong command of written and spoken English on a professional level. It is an advantage if you have been in a pharmaceutical company before and have worked with QMS, GCP, ISO9001 and QA.
You have robust and strong interpersonal skills. You must be detail-oriented with a strong quality mind-set, but take a pragmatic approach to problem solving. You are a team player who thrives with working across departments in an international organisation.
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 Pia Sandau on+45 3075 8334 or Lone Bau on +45 3075 7225.
Deadline
4 August 2013.