QA Technician
- Quality
- Denmark - Måløv
Are you looking for new challenges within QA – development of galenical bulk product for clinical trials and do you want to make a difference? The project portfolio is increasing, and therefore we are looking for a dedicated, professional and enthusiastic new colleague.
About the department
In CMC OPF QA we have the responsibility for quality assurance of oral formulations and release of investigational medicinal products for clinical trials. We have the QA responsibility of the oral pilot production. The department is recently established to support the development of oral protein formulations in our stakeholder departments.
The job
In close cooperation with your 9 colleagues in QA, you act as a consultant for our pilot and formulation departments. The job is a combination of development project and facility related QA tasks. You will review documentation related to manufacturing of drug product for clinical trials, i.e. master batch records, batch documentation, logbooks and SOP’s. You will assure that the documentation is compliant with internal and external requirements.CMC Supply’s continuing high level of audit and inspection readiness is on top on your agenda. In CMC Supply QA we work with QA oversight where you proactive together with your colleagues will identify areas where our stakeholders’ compliance can be strengthened. You have a risk based approach to the development process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
Qualifications
Ideally, you have a background as pharmaconomist, laboratory technician or corresponding qualifications and experience within the pharmaceutical industry. You have knowledge within cGMP and galenical production. You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. Also, you are quite adaptable and challenge our way of doing things, so that we will get even better. You focus on results and quality – and contribute to the right level of compliance.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Janne Lavritsen at+45 3075 7333.
Deadline
6 September 2013.
- Quality
- Denmark - Måløv
Are you looking for new challenges within QA – development of galenical bulk product for clinical trials and do you want to make a difference? The project portfolio is increasing, and therefore we are looking for a dedicated, professional and enthusiastic new colleague.
About the department
In CMC OPF QA we have the responsibility for quality assurance of oral formulations and release of investigational medicinal products for clinical trials. We have the QA responsibility of the oral pilot production. The department is recently established to support the development of oral protein formulations in our stakeholder departments.
The job
In close cooperation with your 9 colleagues in QA, you act as a consultant for our pilot and formulation departments. The job is a combination of development project and facility related QA tasks. You will review documentation related to manufacturing of drug product for clinical trials, i.e. master batch records, batch documentation, logbooks and SOP’s. You will assure that the documentation is compliant with internal and external requirements.CMC Supply’s continuing high level of audit and inspection readiness is on top on your agenda. In CMC Supply QA we work with QA oversight where you proactive together with your colleagues will identify areas where our stakeholders’ compliance can be strengthened. You have a risk based approach to the development process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
Qualifications
Ideally, you have a background as pharmaconomist, laboratory technician or corresponding qualifications and experience within the pharmaceutical industry. You have knowledge within cGMP and galenical production. You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. Also, you are quite adaptable and challenge our way of doing things, so that we will get even better. You focus on results and quality – and contribute to the right level of compliance.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Janne Lavritsen at+45 3075 7333.
Deadline
6 September 2013.