Procurement Professional
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Are you eager to join a great team with a high focus on well-being and personal development? Do you want to learn about how develops and run Clinical Trials by taking part in planning and purchasing materials and clinical products for all clinical trials at ? Then you might be our new colleague! The position We are looking for a purchaser with a high-quality mindset and with a desire to take part in the Supply Chain to conduct clinical trials at . If this sounds like you, we have the perfect opportunity for you!
As part of , Chemical, Manufactoring, Control (CMC) Development & Scaling we make a real difference for patients with chronic diseases across the world. CMC´s key deliveries are to develop, manufacture, and distribute drug candidates, and we assure, that patients for all non-clinical and clinical trials receive trial products at the right time, amount, and quality.
In the Position as a Operational Procurement Professional, the main tasks will be: Timely ordering of materials and Drug Product incl comparators within responsibility of our department, according to corporate requirements and policies Close collaboration with our external vendors and internal stakeholders including follow up on delivery of orders and escalation to production planner, vendor responsible, management and sourcing specialist Drive or participate in process optimisation tasks and projects Ensure anchoring of process optimisation tasks and projects in relevant operational SOP and guidelines or training material Contribute to cLEAN activities with use of LEAN Tools i.e., VSM, A3, SIPOC etc. Update comparator price lists and giving input to risk assessments Timely handling of vendor complaints and customer complains Relevant documentation for purchased goods is collected in due time and timely up-date of KPI’s within purchaser responsibilities Qualifications You hold a master’s degree within Life Sciences such as pharmaceutical sciences, engineering, Supply Chain Planning or similar. You need to be able to handle complex tasks, keep several balls in the air simultaneously, and have a high-quality mindset. Previous working experience within GxP regulated processes is a great advantage.
Ideally, you have: 2-3 years of experience within procurement or comparator sourcing from a regulated environment. Knowledge of how to navigate in a GMP regulated field with several stakeholders. Knowledge about Supply Chain and Lean principles. Experience with documentation; skills within written documentation such as work instructions, training material, change requests and deviations. Fluent in English, and if you speak Danish it is a great advantage.
Personally, you seek simple and effective solutions and see continuous improvement as a natural part of processes, and you are familiar with various LEAN principles.
You are a team player and find motivation when reaching common goals.
About the department Clinical Supplies Supply Chain Planning is a part of Clinical Supplies in CMC Development. We are responsible for the overall planning of the production, packaging, and distribution of products for all clinical trials worldwide. The department consist of five teams, supporting the execution of clinical trials by forecasting/monitoring product demand, ordering product etc, planning the packaging/shipping of Trial Products and supporting the overall trial conduct at the clinical sites with a focus on trial product related processes and systems. Working at
is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact For further information, please contact Lena Vinther Jensen, + Deadline 1. April 2024 Please note that applications will be reviewed on an ongoing basis and interviews will be scheduled as soon as suitable candidates are identified. 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 part of , Chemical, Manufactoring, Control (CMC) Development & Scaling we make a real difference for patients with chronic diseases across the world. CMC´s key deliveries are to develop, manufacture, and distribute drug candidates, and we assure, that patients for all non-clinical and clinical trials receive trial products at the right time, amount, and quality.
In the Position as a Operational Procurement Professional, the main tasks will be:
Ideally, you have:
Personally, you seek simple and effective solutions and see continuous improvement as a natural part of processes, and you are familiar with various LEAN principles.
You are a team player and find motivation when reaching common goals.
About the department Clinical Supplies Supply Chain Planning is a part of Clinical Supplies in CMC Development. We are responsible for the overall planning of the production, packaging, and distribution of products for all clinical trials worldwide. The department consist of five teams, supporting the execution of clinical trials by forecasting/monitoring product demand, ordering product etc, planning the packaging/shipping of Trial Products and supporting the overall trial conduct at the clinical sites with a focus on trial product related processes and systems. Working at
is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact For further information, please contact Lena Vinther Jensen, + Deadline 1. April 2024 Please note that applications will be reviewed on an ongoing basis and interviews will be scheduled as soon as suitable candidates are identified. 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 "Produktchef", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 12.1.2024, 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.
- Produktchef
- Måløv
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