Production Chemist
- Production
- Denmark - Måløv
Are you committed to manage a cleaning validation project and strengthen the support to a tablet production in Novo Nordisk? Right now, we are looking for an experienced candidate with a high quality mindset and GMP experience to join us working in the HRT bulk production of Biopharm Tablets & Finished Products.
About the department
Biopharm T&FP HRT Bulk production is producing HRT (Hormone Replacement Therapy) products. The production consist of the processes; granulation, compression and coating and includes manual cleaning as well as CIP processes. The department consists of 45 employees and is based in Måløv, Denmark. The vacancy is in the Process Support Team that consists of 8 dedicated supporters and a manager.
The job
The primary responsibility of this position will be to manage and perform our cleaning validation in the tablet production and secure that we live the requirements of our quality management system. You will have the responsibility of our cleaning processes and you will handle deviations from standard procedures, implement corrective actions, handle change requests, write protocols and reports and various documentations related to the HRT bulk production. In this job, you will have daily contact with our QA department, Product Support, our Production Team and Technical Team. The department is highly motivated and this position offers you a unique opportunity to strengthen your experience in a GMP production environment, realise personal as well as department goals and see the benefits of your work. You will experience an enthusiastic working climate focused on quality, teamwork and delivery.
Qualification
We imagine you have solid theoretical background, an academic degree (Cand. Pharm, chemical engineer or the equivalent). You have experience with cleaning validation in a pharmaceutical production including experience with ISO 9001 and managing projects in a GMP environment. Preferable you have knowledge of the LEAN principles. On a personal level you have a positive attitude, you are engaged and systematic. You enjoy working with major challenges and can maintain an overview in a busy work day while complying with the requirements of manufacturing drug products. You are flexible in novel situations in a continuously developing environment and you are fluent in both written and spoken Danish and English.
Feel free to submit your job application in either Danish or English whichever you prefer.
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 Julie Månsson on +45 3075 6397.
Deadline
18 August 2013.
- Production
- Denmark - Måløv
Are you committed to manage a cleaning validation project and strengthen the support to a tablet production in Novo Nordisk? Right now, we are looking for an experienced candidate with a high quality mindset and GMP experience to join us working in the HRT bulk production of Biopharm Tablets & Finished Products.
About the department
Biopharm T&FP HRT Bulk production is producing HRT (Hormone Replacement Therapy) products. The production consist of the processes; granulation, compression and coating and includes manual cleaning as well as CIP processes. The department consists of 45 employees and is based in Måløv, Denmark. The vacancy is in the Process Support Team that consists of 8 dedicated supporters and a manager.
The job
The primary responsibility of this position will be to manage and perform our cleaning validation in the tablet production and secure that we live the requirements of our quality management system. You will have the responsibility of our cleaning processes and you will handle deviations from standard procedures, implement corrective actions, handle change requests, write protocols and reports and various documentations related to the HRT bulk production. In this job, you will have daily contact with our QA department, Product Support, our Production Team and Technical Team. The department is highly motivated and this position offers you a unique opportunity to strengthen your experience in a GMP production environment, realise personal as well as department goals and see the benefits of your work. You will experience an enthusiastic working climate focused on quality, teamwork and delivery.
Qualification
We imagine you have solid theoretical background, an academic degree (Cand. Pharm, chemical engineer or the equivalent). You have experience with cleaning validation in a pharmaceutical production including experience with ISO 9001 and managing projects in a GMP environment. Preferable you have knowledge of the LEAN principles. On a personal level you have a positive attitude, you are engaged and systematic. You enjoy working with major challenges and can maintain an overview in a busy work day while complying with the requirements of manufacturing drug products. You are flexible in novel situations in a continuously developing environment and you are fluent in both written and spoken Danish and English.
Feel free to submit your job application in either Danish or English whichever you prefer.
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 Julie Månsson on +45 3075 6397.
Deadline
18 August 2013.