Advanced QC Chemist
Gentofte
Are you driven by continuous optimization and securing a high level of compliance? Are you highly motivated to work in an analytical laboratory and ensure the fast delivery of quality products to our patients? We are looking for a new Chemist to join one of our HPLC teams in Biotech & Rare Disease (BRD) Quality Control (QC) in Gentofte and it might be you! If you are as ambitious as we are, you can look forward to an exciting job in an environment where we always strive to be the best in class in everything we do. The Position
As Analytical QC Chemist you will be responsible for approving analytical results and providing support to laboratory technicians in the analytical work, offering guidance and coaching, to secure timely delivery of analytical results. Additionally, you will collaborate closely with the chemists in the team and ensure that analytical performance and equipment meet industry standards and cGMP. It is essential to have a genuine interest in chromatography and a desire to delve into obtained results to understand analytical variations. The core tasks for the team are: • Ensuring timely delivery of analytical results to our stakeholders to guarantee that medicine reaches the patients.
• Solving laboratory investigations and deviations utilising systematic problem solving methodologies.
• Continuous improvement and optimisation of our processes using cLEAN principles. The role offers an exciting and varied opportunity where you will play a crucial part in ensuring that your team reaches its targets. We aim to work smarter and implement digital and innovative improvements in our processes. This position provides the possibility to influence your daily routines and responsibilities, offering significant opportunities for personal and professional development. Additionally, this role presents the chance to build a strong network within while further developing your skills. Qualifications
We value the following competencies in our new colleague: • Academic degree in chemistry, pharmacy, engineering or related field.
• Experience in the pharmaceutical industry and adherence to cGMP standards.
• Knowledge of chromatographic analysis and HPLC equipment.
• Professional proficiency in both written and spoken Danish and English. As an individual, you are responsible, dedicated, and possess an open-minded approach. Additionally, it should be natural for you to take initiative and be proactive. You excel in creating an overview and have the courage to solve new types of tasks, both individually and in close collaboration with your colleagues and stakeholders. Moreover, you are skilled in maintaining an organized approach to task management and documentation, enabling effective prioritization. About the department
BRD is part of , which delivers products for treatment of rare blood and endocrine disorders. BRD QC consist of six departments supporting our production facilities by performing QC analysis on the whole product portfolio in BRD.
Our department's area of responsibility is chemical, biological, and general compendial analysis of stability samples, drug substance samples, drug product samples and intermediate samples. In our QC department in Gentofte, we are approximately 100 motivated and talented colleagues divided into 6 teams. Your new department is characterized by high professionalism, quality mindset and an informal tone.
Working at BRD,
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
If you want to know more about the position, please contact Julie Kruse Jensen, Associate Manager at +.
Deadline
23 June 2024. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying for this job in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
As Analytical QC Chemist you will be responsible for approving analytical results and providing support to laboratory technicians in the analytical work, offering guidance and coaching, to secure timely delivery of analytical results. Additionally, you will collaborate closely with the chemists in the team and ensure that analytical performance and equipment meet industry standards and cGMP. It is essential to have a genuine interest in chromatography and a desire to delve into obtained results to understand analytical variations. The core tasks for the team are: • Ensuring timely delivery of analytical results to our stakeholders to guarantee that medicine reaches the patients.
• Solving laboratory investigations and deviations utilising systematic problem solving methodologies.
• Continuous improvement and optimisation of our processes using cLEAN principles. The role offers an exciting and varied opportunity where you will play a crucial part in ensuring that your team reaches its targets. We aim to work smarter and implement digital and innovative improvements in our processes. This position provides the possibility to influence your daily routines and responsibilities, offering significant opportunities for personal and professional development. Additionally, this role presents the chance to build a strong network within while further developing your skills. Qualifications
We value the following competencies in our new colleague: • Academic degree in chemistry, pharmacy, engineering or related field.
• Experience in the pharmaceutical industry and adherence to cGMP standards.
• Knowledge of chromatographic analysis and HPLC equipment.
• Professional proficiency in both written and spoken Danish and English. As an individual, you are responsible, dedicated, and possess an open-minded approach. Additionally, it should be natural for you to take initiative and be proactive. You excel in creating an overview and have the courage to solve new types of tasks, both individually and in close collaboration with your colleagues and stakeholders. Moreover, you are skilled in maintaining an organized approach to task management and documentation, enabling effective prioritization. About the department
BRD is part of , which delivers products for treatment of rare blood and endocrine disorders. BRD QC consist of six departments supporting our production facilities by performing QC analysis on the whole product portfolio in BRD.
Our department's area of responsibility is chemical, biological, and general compendial analysis of stability samples, drug substance samples, drug product samples and intermediate samples. In our QC department in Gentofte, we are approximately 100 motivated and talented colleagues divided into 6 teams. Your new department is characterized by high professionalism, quality mindset and an informal tone.
Working at BRD,
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
If you want to know more about the position, please contact Julie Kruse Jensen, Associate Manager at +.
Deadline
23 June 2024. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying for this job in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Gentofte.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Gentofte