QA Specialist - SAP Master Data
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Søborg
Want to use your strong analytical and problem-solving skills to support
Then apply now to join us for a life-changing career!
The position
As a QA Specialist - SAP Master Data in the QA Training and System Support team, you will be part of a team working across Global Contract Manufacturing (GMC) Drug Product and Drug Substance QA - which is responsible for supporting the QA project & operations teams in the department in close collaboration with our Line of Business; we are besides Digital Certificate Solution project involved in the upgrading SAP ECC to SAP4Hana and the Digital Batch Release project, so we are able to serve even more patients. Main responsibilities will include to: • Lead projects for new CMOs partnerships by building material masters in SAP ECC as well as maintenance of the data
• Create a CoA (Certificate of Analysis) Master Data and CoC (Certificate of Com-pliance)
• Set direction of how to set up new products for QA release
• Provide guidance and support for data-related inquiries, troubleshooting, and issue resolution specific to master data creation for new CMOs
• Participate in system enhancement projects and provide expertise on best practices for SAP master data management related to new CMOs Another focus for this position will be for you to act as Product owner for GCM QA in the Digital Solution Project and work 2 days per week in the Product owner team lo-cated in Ballerup. Overall, you will solve a wide variety of tasks and have a great opportunity to be chal-lenged every day in a job with lots of professional interfaces working with many stakeholders both internally and externally, collaborating closely with cross-functional teams to facilitate the setup and maintenance of master data for new CMO operations, supporting efficient and compliant data exchange. At the moment, the workplace is in Søborg but in February we will be relocated to Høje Taastrup.
Qualifications
We are looking for someone who has a track record of working with SAP ECC, experi-ence as Product Owner and knowledge about the QA release process and the use of Certificates. The ideal candidate for this position is:
• A Bachelor’s or Masters’s graduate as a Pharmacist, Engineer or similar
• Very experienced in SAP master data management within QA
• A skilled professional within a GMP regulated industry (pharmaceutical, medical devices, food production)
• Someone who thrives on working across departments in an international organ-ization
• A great communicator and collaborator, with a professional proficiency in Eng-lish On a personal level, you are open-minded with strong analytical skill, result-oriented paired with highly structured working style and good sense of responsibility, flexibility and team player mindset.
About the department
Our organization is expanding as we continue to support the strong volume growth with capacity expansions at CMOs, a growing R&D pipeline progressing towards mar-kets with CMO supply chains and acquired companies with fully outsourced CMO supply chain. At present, our department is composed of 70 highly skilled employees who are dedi-cated to operations in aseptic or finished product areas, projects, and support func-tions. We are in a phase of continuous growth and anticipate expanding even further in the future.
The department is characterized by a high level of professionalism, flexibility, and cooperation. We can offer a great working environment with high level of team spirit as well as a highly skilled team of ambitious and engaged colleagues. We share an informal tone, and enjoy learning from each other, striving to deepen our understanding of a com-plex area. We focus on good social relations and prioritise to make room for fun at work. Discover the cutting-edge technologies behind 's life-changing innova-tions at TechLife at . From AI to quantum computing, our digital experts push boundaries and make a tangible impact on lives across the globe. 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 Marianne Hjulgaard on + or to Esben Holm Hjørringgaard + Deadline
14 November 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.
Digital Projects? Ready to participate in building of master data for new and existing Contract Manufacturing Organizations (CMO’s)? Do you want to be part of this digital journey and bring your experience within Manufacturing and SAP into play? Then apply now to join us for a life-changing career!
The position
As a QA Specialist - SAP Master Data in the QA Training and System Support team, you will be part of a team working across Global Contract Manufacturing (GMC) Drug Product and Drug Substance QA - which is responsible for supporting the QA project & operations teams in the department in close collaboration with our Line of Business; we are besides Digital Certificate Solution project involved in the upgrading SAP ECC to SAP4Hana and the Digital Batch Release project, so we are able to serve even more patients. Main responsibilities will include to: • Lead projects for new CMOs partnerships by building material masters in SAP ECC as well as maintenance of the data
• Create a CoA (Certificate of Analysis) Master Data and CoC (Certificate of Com-pliance)
• Set direction of how to set up new products for QA release
• Provide guidance and support for data-related inquiries, troubleshooting, and issue resolution specific to master data creation for new CMOs
• Participate in system enhancement projects and provide expertise on best practices for SAP master data management related to new CMOs Another focus for this position will be for you to act as Product owner for GCM QA in the Digital Solution Project and work 2 days per week in the Product owner team lo-cated in Ballerup. Overall, you will solve a wide variety of tasks and have a great opportunity to be chal-lenged every day in a job with lots of professional interfaces working with many stakeholders both internally and externally, collaborating closely with cross-functional teams to facilitate the setup and maintenance of master data for new CMO operations, supporting efficient and compliant data exchange. At the moment, the workplace is in Søborg but in February we will be relocated to Høje Taastrup.
Qualifications
We are looking for someone who has a track record of working with SAP ECC, experi-ence as Product Owner and knowledge about the QA release process and the use of Certificates. The ideal candidate for this position is:
• A Bachelor’s or Masters’s graduate as a Pharmacist, Engineer or similar
• Very experienced in SAP master data management within QA
• A skilled professional within a GMP regulated industry (pharmaceutical, medical devices, food production)
• Someone who thrives on working across departments in an international organ-ization
• A great communicator and collaborator, with a professional proficiency in Eng-lish On a personal level, you are open-minded with strong analytical skill, result-oriented paired with highly structured working style and good sense of responsibility, flexibility and team player mindset.
About the department
Our organization is expanding as we continue to support the strong volume growth with capacity expansions at CMOs, a growing R&D pipeline progressing towards mar-kets with CMO supply chains and acquired companies with fully outsourced CMO supply chain. At present, our department is composed of 70 highly skilled employees who are dedi-cated to operations in aseptic or finished product areas, projects, and support func-tions. We are in a phase of continuous growth and anticipate expanding even further in the future.
The department is characterized by a high level of professionalism, flexibility, and cooperation. We can offer a great working environment with high level of team spirit as well as a highly skilled team of ambitious and engaged colleagues. We share an informal tone, and enjoy learning from each other, striving to deepen our understanding of a com-plex area. We focus on good social relations and prioritise to make room for fun at work. Discover the cutting-edge technologies behind 's life-changing innova-tions at TechLife at . From AI to quantum computing, our digital experts push boundaries and make a tangible impact on lives across the globe. 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 Marianne Hjulgaard on + or to Esben Holm Hjørringgaard + Deadline
14 November 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 Søborg.
Jobbet er oprettet på vores service den 31.10.2024, 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.
- 31.10.2024
- Øvrige
- Søborg
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