Process Supporter
- Production
- Denmark - Måløv
Are you committed to support a GMP production in Novo Nordisk? Right now, we are looking for a production chemist with a high quality mindset and GMP experience to join us in the HRT bulk production, a part of Biopharm Tablets & Finished Products.
About the department
The job is located in Biopharm T&FP HRT Bulk production, which is a tablet production producing HRT (Hormone Replacement Therapy) products including the processes; granulation, compression and coating. The department consists of 50 employees and is based in Måløv, Denmark and consists of three teams; Production, Tech Support and Process Support. The Process Support Team consists of 10 dedicated supporters.
The job
The primary responsibilities of this position will be to support the operators in the daily production and secure that we live the requirements of our quality management system and that we work systematically according to the LEAN principles implemented in the department. Furthermore, you will handle deviations from standard procedures, implement corrective actions, handle change requests, write protocols, reports and various documentations related to the HRT bulk production. You will also be a part of the team releasing the bulk batches. In this job, you will be in close contact with professional colleagues both in the department as well as in QA and QC department, Product Support and our Technical Team.
Our 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 where we take a personal responsibility for quality, delivery and each other.
Qualifications
You hold an academic degree (Cand. Pharm, chemical engineer or the equivalent). You have experience from pharmaceutical and knows how to perform in a GMP environment. Preferable you have knowledge of the LEAN principles. On a personal level you have a positive can-do attitude, you are engaged, systematic and take responsibility to ensure deadlines are met. You enjoy working with major challenges and can maintain an overview in a busy work day while complying with the requirements for manufacturing of drug products. You are fluent in both written and spoken Danish and English.
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 Charlotte Lex on +45 3075 2559.
Deadline
6 January 2014
- Production
- Denmark - Måløv
Are you committed to support a GMP production in Novo Nordisk? Right now, we are looking for a production chemist with a high quality mindset and GMP experience to join us in the HRT bulk production, a part of Biopharm Tablets & Finished Products.
About the department
The job is located in Biopharm T&FP HRT Bulk production, which is a tablet production producing HRT (Hormone Replacement Therapy) products including the processes; granulation, compression and coating. The department consists of 50 employees and is based in Måløv, Denmark and consists of three teams; Production, Tech Support and Process Support. The Process Support Team consists of 10 dedicated supporters.
The job
The primary responsibilities of this position will be to support the operators in the daily production and secure that we live the requirements of our quality management system and that we work systematically according to the LEAN principles implemented in the department. Furthermore, you will handle deviations from standard procedures, implement corrective actions, handle change requests, write protocols, reports and various documentations related to the HRT bulk production. You will also be a part of the team releasing the bulk batches. In this job, you will be in close contact with professional colleagues both in the department as well as in QA and QC department, Product Support and our Technical Team.
Our 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 where we take a personal responsibility for quality, delivery and each other.
Qualifications
You hold an academic degree (Cand. Pharm, chemical engineer or the equivalent). You have experience from pharmaceutical and knows how to perform in a GMP environment. Preferable you have knowledge of the LEAN principles. On a personal level you have a positive can-do attitude, you are engaged, systematic and take responsibility to ensure deadlines are met. You enjoy working with major challenges and can maintain an overview in a busy work day while complying with the requirements for manufacturing of drug products. You are fluent in both written and spoken Danish and English.
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 Charlotte Lex on +45 3075 2559.
Deadline
6 January 2014