Senior GMP Supporter
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Køge
Are you ready to make an impact in the pharmaceutical industry? Join our team at Novo Nordisk Pharmatech in Køge as a Senior GMP supporter and play a vital role in ensuring the highest quality standards from our contract manufacturing partners. If you thrive in a dynamic environment and have a passion for quality, we want to hear from you! As Senior GMP Supporter within Excipient production you will mainly support our outsourced product production at selected CMOs (Contract Manufacturing Organizations) The primary responsibility of the position is to act as our GMP support for excipient manufacturing in project teams with a special focus on facility, equipment and QMS, and you will be an important interface between the Novo Nordisk Pharmatech stakeholders and our external manufacturing partners.
The Job To be the ideal candidate for this position, we image that you:
• Have insights into technical process equipment
• Thrive in a cross-functional team
• Can author and review project documentation, deviations, batch records, change requests etc.
• Are motivated by gaining knowledge of the production through the project work, including the chemistry behind the process, the production equipment, the facility and other processes related to manufacturing We expect you to make procedural or process suggestions for achieving team goals or performing team functions; providing necessary resources and help to remove obstacles, ensuring the team accomplishes specific results.
Qualifications You are an outgoing person that always seeks solutions to achieve the best outcome for the team and organization but never compromises on quality. You will have a wide variety of stakeholders, therefore the ability to work across boundaries is critical for your success. • Master’s Degree within a relevant area, e.g. Biochemistry, Pharmacy, Engineering or similar
• Theoretical background is combined with 4+ years of practical experience within the pharmaceutical industry and manufacturing of pharmaceutical products under GMP
• You should be able to demonstrate knowledge of excipient or API production within e.g. protein / enzyme production
• Knowledge within SAP is an advantage
• You have an analytical mind-set with the ability to work in a structured way and an ability to support multiple activities
• Strong communication skills in the English language As a person you are good at building trust with stakeholders, and you naturally share important and relevant information with your team. Working location will be in Køge 45 minutes from Copenhagen and since international collaboration is an integrated part of your job, you can expect to be travelling around 10 days per year.
About the department
The Manufacturing Development department in Novo Nordisk Pharmatech consists of 30 dedicated employees split into three teams. You will become a senior GMP supporter in the PSG PM and Contract Manufacturing team consisting of 9 chemists, supporters and Project Managers. This team ensures a successful setup of the CMO collaborations as well as project planning for the developed products from development to commercial production on site.
We work in close collaboration with our customers to develop optimal purification solutions for new and existing molecules used for the treatment of many different conditions as well as process enzymes crucial for bioprocessing of established and upcoming therapeutic moieties. The atmosphere is relaxed, creative and characterized by our growth mindset.
Working at Novo Nordisk Pharmatech A/S
Novo Nordisk Pharmatech A/S has 300+ employees and is 100% owned by Novo Nordisk A/S. The ability of Novo Nordisk Pharmatech A/S to produce and deliver quality products to the pharmaceutical industry, combined with our complete range of services within regulatory requirements, makes us a preferred supplier to many global pharmaceutical companies. Novo Nordisk Pharmatech A/S is a fast-growing company, which is generating many exciting projects and excellent development opportunities. Contact
For further information please contact Manager Christin Schäfer at +45 2429 4151 Deadline
20th August 2023.
Applications will be screened on an ongoing basis, and we regularly call for interviews.
Please do not hesitate to apply by simply uploading your CV. You don’t need to write a cover letter, but please add a few lines on why you are motivated by this position in your resume.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk 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.
The Job To be the ideal candidate for this position, we image that you:
• Have insights into technical process equipment
• Thrive in a cross-functional team
• Can author and review project documentation, deviations, batch records, change requests etc.
• Are motivated by gaining knowledge of the production through the project work, including the chemistry behind the process, the production equipment, the facility and other processes related to manufacturing We expect you to make procedural or process suggestions for achieving team goals or performing team functions; providing necessary resources and help to remove obstacles, ensuring the team accomplishes specific results.
Qualifications You are an outgoing person that always seeks solutions to achieve the best outcome for the team and organization but never compromises on quality. You will have a wide variety of stakeholders, therefore the ability to work across boundaries is critical for your success. • Master’s Degree within a relevant area, e.g. Biochemistry, Pharmacy, Engineering or similar
• Theoretical background is combined with 4+ years of practical experience within the pharmaceutical industry and manufacturing of pharmaceutical products under GMP
• You should be able to demonstrate knowledge of excipient or API production within e.g. protein / enzyme production
• Knowledge within SAP is an advantage
• You have an analytical mind-set with the ability to work in a structured way and an ability to support multiple activities
• Strong communication skills in the English language As a person you are good at building trust with stakeholders, and you naturally share important and relevant information with your team. Working location will be in Køge 45 minutes from Copenhagen and since international collaboration is an integrated part of your job, you can expect to be travelling around 10 days per year.
About the department
The Manufacturing Development department in Novo Nordisk Pharmatech consists of 30 dedicated employees split into three teams. You will become a senior GMP supporter in the PSG PM and Contract Manufacturing team consisting of 9 chemists, supporters and Project Managers. This team ensures a successful setup of the CMO collaborations as well as project planning for the developed products from development to commercial production on site.
We work in close collaboration with our customers to develop optimal purification solutions for new and existing molecules used for the treatment of many different conditions as well as process enzymes crucial for bioprocessing of established and upcoming therapeutic moieties. The atmosphere is relaxed, creative and characterized by our growth mindset.
Working at Novo Nordisk Pharmatech A/S
Novo Nordisk Pharmatech A/S has 300+ employees and is 100% owned by Novo Nordisk A/S. The ability of Novo Nordisk Pharmatech A/S to produce and deliver quality products to the pharmaceutical industry, combined with our complete range of services within regulatory requirements, makes us a preferred supplier to many global pharmaceutical companies. Novo Nordisk Pharmatech A/S is a fast-growing company, which is generating many exciting projects and excellent development opportunities. Contact
For further information please contact Manager Christin Schäfer at +45 2429 4151 Deadline
20th August 2023.
Applications will be screened on an ongoing basis, and we regularly call for interviews.
Please do not hesitate to apply by simply uploading your CV. You don’t need to write a cover letter, but please add a few lines on why you are motivated by this position in your resume.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk 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 Køge.
Jobbet er oprettet på vores service den 18.7.2023, 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.
- Øvrige
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