Advanced QA Professional
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Værløse
Are you ready to play a crucial role in ensuring the quality and safety of our products for patients worldwide? Do you thrive in a challenging and ever-changing environment? Would you like to help us on our journey of an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and capacity expansions as well as personal development? If your response to this questions is yes, then you may be our new colleague in Biotech and Rare Disease (BRD) QA,apply today and join us for a life changing career! The position
As a Quality Assurance (QA) professional you are the gatekeeper for Good Manufacturing Practice (GMP) compliance. After a period of introduction and training it will be one of your primary responsibilities to ensure compliance through review of batch documentation and status assignment of assembly and packaging orders according to GMP and our Standard Operating Procedures (SOP). Based on your experience, future tasks can entail quality assurance of our many exciting validation projects.
As part of the QA team, you will have the opportunity to work with highly skilled people and get a solid understanding of GMP and manufacturing processes in a packaging department. The work environment is informal, and the team is characterized by a high-quality mind-set and a cooperative spirit.
Qualifications
To succeed in this job, it is important to have great communication skills, other than a close and good collaboration with our production and being able to communicate with a wide range of people, also by being present in our production facilities. The ideal candidate has: • a master’s degree in pharmacy, engineering or similar
• some experience in QA/production related roles in the pharmaceutical industry
• GMP knowledge
• full English proficiency, and at least reading understanding of Danish It will be an advantage if you have some level of IT flair and knowledge of digitalization tools, as we are facing a lot of new exciting opportunities to improve our processes through digitalization. Finally, your drivers are a great personal commitment and accountability in every aspect of your work. We urge you to apply no matter your previous experience. Both newcomers and very experienced candidates are more than welcome to apply. We have great opportunities for personal and professional development for all. About the department
We are a diverse department with 29 employees divided into two areas within BRD QA. We are responsible for the quality assurance of our pharmaceutical products of assembled and finished packed products. You will become part of a dedicated team of academics in a casual atmosphere and where we take good care of each other. The team covers two separate packaging departments located in Værløse (assembly and packaging) and Gentofte (packaging). Our department is in an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and personal development. Working at At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Manager Benedicte Hvidberg at +. Deadline
26 May 2024 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.
As a Quality Assurance (QA) professional you are the gatekeeper for Good Manufacturing Practice (GMP) compliance. After a period of introduction and training it will be one of your primary responsibilities to ensure compliance through review of batch documentation and status assignment of assembly and packaging orders according to GMP and our Standard Operating Procedures (SOP). Based on your experience, future tasks can entail quality assurance of our many exciting validation projects.
As part of the QA team, you will have the opportunity to work with highly skilled people and get a solid understanding of GMP and manufacturing processes in a packaging department. The work environment is informal, and the team is characterized by a high-quality mind-set and a cooperative spirit.
Qualifications
To succeed in this job, it is important to have great communication skills, other than a close and good collaboration with our production and being able to communicate with a wide range of people, also by being present in our production facilities. The ideal candidate has: • a master’s degree in pharmacy, engineering or similar
• some experience in QA/production related roles in the pharmaceutical industry
• GMP knowledge
• full English proficiency, and at least reading understanding of Danish It will be an advantage if you have some level of IT flair and knowledge of digitalization tools, as we are facing a lot of new exciting opportunities to improve our processes through digitalization. Finally, your drivers are a great personal commitment and accountability in every aspect of your work. We urge you to apply no matter your previous experience. Both newcomers and very experienced candidates are more than welcome to apply. We have great opportunities for personal and professional development for all. About the department
We are a diverse department with 29 employees divided into two areas within BRD QA. We are responsible for the quality assurance of our pharmaceutical products of assembled and finished packed products. You will become part of a dedicated team of academics in a casual atmosphere and where we take good care of each other. The team covers two separate packaging departments located in Værløse (assembly and packaging) and Gentofte (packaging). Our department is in an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and personal development. Working at At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Manager Benedicte Hvidberg at +. Deadline
26 May 2024 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 Værløse.
Jobbet er oprettet på vores service den 13.5.2024, 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.
- 13.05.2024
- Øvrige
- Værløse
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