Experienced Supporter to Future QC
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Are you ready to design and build our new Future QC Project to ensure a facility that can accommodate our high ambitions for automation and the future way to do QC testing - then take a further look at this very exciting position. The position We are looking for an experienced supporter to join our Future QC Project, with anchor in our QC Processes department. The department has the responsibility to secure that our new facility will live up to all requirements and to accommodate the future automation within QC testing. We are looking for a new member to our QC Support area. As a team player with strong collaboration and communication skills you will play a key role by putting your know-how into use and help us build new critical processes across all Future QC departments. You will be part of designing the layout of the future laboratories together with end-users and specialists. Examples of your daily tasks could be one or more of the following: • Participate in a highly important project of introducing new fully automated process and equipment where needed.
• Supervise facility design, for example Sample Receiving area, Goods Receiving area, or Laboratory Utensil Washing area.
• Collect, structure, and visualise the required data to support selection of designs and equipment solutions.
• Develop and optimize the processes in Future QC, and plan/facilitate workshops.
• Qualification of equipment, incl. relevant experience in verification activities and documentation (FAT, SAT, IQ, and OQ).
• Coordinate/support and ensure execution of all activities necessary to build the Joined Facilities and relocate the existing processes into our new laboratory facility.
• Responsible for creating a set-up and governance that ensures maintaining the established processes/equipment after implementation. Moreover, you will be expected to identify challenges and secure the necessary agreements/clarifications with stakeholders such as architects, consulting engineers, suppliers, end-users, QA, regulatory and IT. This also entails being curious about how other teams and departments work, both within and outside . Qualifications The ideal candidate for this position should possess the following qualifications: • A relevant educational background within life sciences, or other relevant technical background, preferably with 3+ years of experience from a QC function in the pharmaceutical industry.
• Strong communication skills in both written and spoken English and Danish, with a natural ability to establish new relationships across teams and departments.
• Strong collaboration skills, with the ability to set direction and motivate less experienced colleagues or stakeholders. Furthermore, the ideal candidate preferable has one or more of the following qualifications: • Experience with qualifying laboratory equipment and/or facility areas/processes.
• A strong Lean-methodology toolbox, combined with a natural passion for doing things smarter.
• A project management toolbox to enable a structured approach.
On a personal level you have the right quality mindset and dare to challenge our way of working and are known for your ability to identify improvements, as well as taking the lead for driving the implementation of these improvements. About the project The Future QC Project will build a multi-functional QC laboratory at located on Zealand and be the future workplace for many QC colleagues. In the Project both Joint Facilities, Chemistry and Microbiological QC laboratories will be established, as well as development laboratories within these areas. When operational the laboratories will deliver analytical support to production units across covering products for treatment of diabetes, obesity, rare blood, and endocrine disorders. The laboratories will be ready for our ambitious goals for QC Automation & Digitalisation. 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 If you want to hear more about the position, contact Heidi Ardal Larsen on +.
Deadline 1 April, 2024 We may conduct interviews before the deadline. Therefore, we may take the liberty to close for new applicants before the deadline.
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.
• Supervise facility design, for example Sample Receiving area, Goods Receiving area, or Laboratory Utensil Washing area.
• Collect, structure, and visualise the required data to support selection of designs and equipment solutions.
• Develop and optimize the processes in Future QC, and plan/facilitate workshops.
• Qualification of equipment, incl. relevant experience in verification activities and documentation (FAT, SAT, IQ, and OQ).
• Coordinate/support and ensure execution of all activities necessary to build the Joined Facilities and relocate the existing processes into our new laboratory facility.
• Responsible for creating a set-up and governance that ensures maintaining the established processes/equipment after implementation. Moreover, you will be expected to identify challenges and secure the necessary agreements/clarifications with stakeholders such as architects, consulting engineers, suppliers, end-users, QA, regulatory and IT. This also entails being curious about how other teams and departments work, both within and outside . Qualifications The ideal candidate for this position should possess the following qualifications: • A relevant educational background within life sciences, or other relevant technical background, preferably with 3+ years of experience from a QC function in the pharmaceutical industry.
• Strong communication skills in both written and spoken English and Danish, with a natural ability to establish new relationships across teams and departments.
• Strong collaboration skills, with the ability to set direction and motivate less experienced colleagues or stakeholders. Furthermore, the ideal candidate preferable has one or more of the following qualifications: • Experience with qualifying laboratory equipment and/or facility areas/processes.
• A strong Lean-methodology toolbox, combined with a natural passion for doing things smarter.
• A project management toolbox to enable a structured approach.
On a personal level you have the right quality mindset and dare to challenge our way of working and are known for your ability to identify improvements, as well as taking the lead for driving the implementation of these improvements. About the project The Future QC Project will build a multi-functional QC laboratory at located on Zealand and be the future workplace for many QC colleagues. In the Project both Joint Facilities, Chemistry and Microbiological QC laboratories will be established, as well as development laboratories within these areas. When operational the laboratories will deliver analytical support to production units across covering products for treatment of diabetes, obesity, rare blood, and endocrine disorders. The laboratories will be ready for our ambitious goals for QC Automation & Digitalisation. 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 If you want to hear more about the position, contact Heidi Ardal Larsen on +.
Deadline 1 April, 2024 We may conduct interviews before the deadline. Therefore, we may take the liberty to close for new applicants before the deadline.
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 Bagsværd.
Jobbet er oprettet på vores service den 14.3.2024, 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.
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