Senior QC Professional
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Hillerød
Are you driven by taking responsibility, setting direction, and ensuring high standards in Quality Control (QC) for both new and existing products? Do you have a passion for chemical analysis and a desire to lead the transformation of processes toward increased automation, digitalization, and optimization while maintaining a high level of compliance?
If so, you could be the experienced QC Professional we are looking for. Apply now for a life-changing career! The position
As a Senior QC Professional, you will work in close collaboration with the QC chemists, laboratory technicians and QC Area Specialist to ensure that the analytical performance and equipment live up to industry standards, GMP and regulatory requirements (ICH guidelines, pharmacopeia, etc.)
Your responsibilities will include: Serving as the method responsible chemist, ensuring alignment between product requirements and QC analyses.
Approving and supporting delivery of analytical results within lead time, while supporting documentation preparation for customers and authorities.
Leading the transfer and implementation of new analytical methods as well as new digital and automated solutions in current processes.
Driving continuous improvement and optimization of processes, including systematic problem solving (SPS).
Collaborating with stakeholders across the organization, participating in projects and facilitating audits and inspections.
Working within GMP requirements, managing Change Requests, updating SOPs, and handling deviations, including OOS/OOT/OOE incidents, are integral aspects of the role.
Qualifications
To succeed in this role, you have: A scientific academic degree such as cand. pharm., cand. scient., chemical engineer or similar; a Ph.D. in a relevant area could be an advantage.
Experience from a GMP-regulated laboratory.
Working experience as an analytical chemist with techniques such as HPLC, GC, titration and Spectrophotometer.
Relevant LEAN experience from a comparable position or education, combined with a natural eye for upscaling work processes and reduce waste is an advantage.
Strong communication skills and professionally proficient in both written and spoken Danish and English.
Moreover, it will be considered an advantage if you have scientific experience within analytical work, impurity profiles and validation of QC methods. On a personal level, you are a team player with a solution-oriented mindset and a positive attitude. You bring strong analytical skills while maintaining a broad perspective. You thrive in a dynamic, collaborative environment with frequent interaction both within and outside the team. Meeting deadlines is important to you, and you excel at doing so. We value candidates who embrace change and proactively suggest new solutions, processes, and improvements. You are adaptable in a fast-paced setting where priorities can shift quickly. A good sense of humor and a strong drive for success are highly appreciated in our team culture. About the department
The QC department in AMSAT QC consists of 75 employees divided into 4 teams. You will be joining a team of 20 highly professional and motivated chemists, laboratory technicians, an operator, a student assistant and a GMP Coordinator. We perform a wide range of chemical drug product analysis, as well as mechanical injection tests on insulin pens. We work with many stakeholders across the organization and have a broad interface with other QC areas in .
Daily delivery of analytical results is in focus and the working pace is high. We continuously look to optimize and stabilize our processes to improve lead time. To ensure that medicine reaches the patients in due time, one of the focus areas in QC is not to be delayed the final release of the products.
Working at
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 energize 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
For further information, you can contact Associate Manager, Sultan Colak on +.
Deadline
09 September 2024.
Please submit your resume in English. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying 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.
If so, you could be the experienced QC Professional we are looking for. Apply now for a life-changing career! The position
As a Senior QC Professional, you will work in close collaboration with the QC chemists, laboratory technicians and QC Area Specialist to ensure that the analytical performance and equipment live up to industry standards, GMP and regulatory requirements (ICH guidelines, pharmacopeia, etc.)
Your responsibilities will include:
Qualifications
To succeed in this role, you have:
Moreover, it will be considered an advantage if you have scientific experience within analytical work, impurity profiles and validation of QC methods. On a personal level, you are a team player with a solution-oriented mindset and a positive attitude. You bring strong analytical skills while maintaining a broad perspective. You thrive in a dynamic, collaborative environment with frequent interaction both within and outside the team. Meeting deadlines is important to you, and you excel at doing so. We value candidates who embrace change and proactively suggest new solutions, processes, and improvements. You are adaptable in a fast-paced setting where priorities can shift quickly. A good sense of humor and a strong drive for success are highly appreciated in our team culture. About the department
The QC department in AMSAT QC consists of 75 employees divided into 4 teams. You will be joining a team of 20 highly professional and motivated chemists, laboratory technicians, an operator, a student assistant and a GMP Coordinator. We perform a wide range of chemical drug product analysis, as well as mechanical injection tests on insulin pens. We work with many stakeholders across the organization and have a broad interface with other QC areas in .
Daily delivery of analytical results is in focus and the working pace is high. We continuously look to optimize and stabilize our processes to improve lead time. To ensure that medicine reaches the patients in due time, one of the focus areas in QC is not to be delayed the final release of the products.
Working at
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 energize 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
For further information, you can contact Associate Manager, Sultan Colak on +.
Deadline
09 September 2024.
Please submit your resume in English. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying 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 Hillerød.
Jobbet er oprettet på vores service den 19.8.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- 19.08.2024
- Øvrige
- Hillerød
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