Logistics Coordinator with GMP experience
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Logistics Coordinator with GMP experienceDo you want to take part in a growth journey where we are establishing a new area of responsibility in a small newly created team? Do you like to think innovative, set direction, and drive optimization? Are you curious to use your GMP knowledge, experience, and mindset in a shipping centralized context? Do you see yourself use your excellent communication skills and stakeholder service come to play to make ends meet and ensure timely shipping of pharmaceutical substances in compliance?
Then you could be the one we are looking for to strengthen our CMC Shipping ‘magician’ team. Apply today!
The Position
In your new role you will have the responsibility to:
• Secure that operations are in compliance with regulatory requirements.
• Update and maintain our SOPs and Guidelines.
• Contribute to an inspection ready culture.
• Coordinate, oversee and complete shipments of both GMP and non-GMP materials, in the development of new pharmaceuticals used in clinical trials.
• Drive improvement projects focusing on stakeholder interaction and IT-interfaces.
You will work closely together with project managers, both internal and external, where you will use both your GMP and GDP expertise, as well as your highly collaborative skills to find the optimal transport solution for moving clinical trial materials across the world. You will furthermore use your customer centric focus when working together with other internal and external stakeholders such as logistics services, material suppliers, QA etc, to ensure that sufficient knowledge safeguards patients when discovering and developing new pharmaceuticals.
We offer an evolving position as part of a dynamic, social, and multidisciplinary team with a high degree of autonomy. Continuous improvements and process optimizations is an integrated part of our daily work as CMC Shipping is a new area of responsibility and continuously growing. We focus on cutting complexity, as we build our future-oriented team.
Qualifications
To be considered for this position, we expect you to:
• Hold a scientific academic degree in pharmacy, biology, chemistry, or another relevant discipline.
• Have 2-3 years of experience working within one of these areas: Quality Assurance, GMP in the pharmaceutical industry or Freight Forwarding in connection to pharmaceutical products.
• You take a systematic approach to problem solving and have a strong quality mindset.
• You are proficient in both spoken and written English.
As a person, you have/are:
• The ability to navigate a complex stakeholder landscape to drive outcomes, where you will use your effective communication and interpersonal skills to drive extensive collaborations.
• Structured, a natural sense of priority and not afraid to set direction.
• An empathic team-player.
• Thrive in a changing and dynamic work environment.
The Department
The department Virology and Raw Materials is a part of CMC API Development and consists of 50+ colleagues organized in 4 teams. Your new team consists of 5 colleagues situated in Bagsværd who enjoy social interaction especially expressed through breakfast every Tuesday, walking/running every Wednesday, and a plank challenge almost every week. In CMC Shipping we are dedicated, knowledgeable, indeed knowledge sharing, fun, and open-minded. The position is office based, but we do offer some flexibility by working from home, if the task at hand allows it.
Working at Novo Nordisk
Novo Nordisk 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 Novo Nordisk is working toward something bigger than ourselves, and it's a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 57,000 employees. Together, we go further. Together, we're life changing.
Contact
For further information, please contact Associate Manager,
Marit Klette at +45 3077 6875
Deadline
11th of June 2023
We will review applications and invite for interviews on a continuous basis.
You do not need to write a cover letter, but please write approx. 10-15 lines in your CV about your motivation for the job, highlighting your key skills and contributions to the job. In addition, please avoid the use of photos in your CV. This makes for a better and more fair process. 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.
Then you could be the one we are looking for to strengthen our CMC Shipping ‘magician’ team. Apply today!
The Position
In your new role you will have the responsibility to:
• Secure that operations are in compliance with regulatory requirements.
• Update and maintain our SOPs and Guidelines.
• Contribute to an inspection ready culture.
• Coordinate, oversee and complete shipments of both GMP and non-GMP materials, in the development of new pharmaceuticals used in clinical trials.
• Drive improvement projects focusing on stakeholder interaction and IT-interfaces.
You will work closely together with project managers, both internal and external, where you will use both your GMP and GDP expertise, as well as your highly collaborative skills to find the optimal transport solution for moving clinical trial materials across the world. You will furthermore use your customer centric focus when working together with other internal and external stakeholders such as logistics services, material suppliers, QA etc, to ensure that sufficient knowledge safeguards patients when discovering and developing new pharmaceuticals.
We offer an evolving position as part of a dynamic, social, and multidisciplinary team with a high degree of autonomy. Continuous improvements and process optimizations is an integrated part of our daily work as CMC Shipping is a new area of responsibility and continuously growing. We focus on cutting complexity, as we build our future-oriented team.
Qualifications
To be considered for this position, we expect you to:
• Hold a scientific academic degree in pharmacy, biology, chemistry, or another relevant discipline.
• Have 2-3 years of experience working within one of these areas: Quality Assurance, GMP in the pharmaceutical industry or Freight Forwarding in connection to pharmaceutical products.
• You take a systematic approach to problem solving and have a strong quality mindset.
• You are proficient in both spoken and written English.
As a person, you have/are:
• The ability to navigate a complex stakeholder landscape to drive outcomes, where you will use your effective communication and interpersonal skills to drive extensive collaborations.
• Structured, a natural sense of priority and not afraid to set direction.
• An empathic team-player.
• Thrive in a changing and dynamic work environment.
The Department
The department Virology and Raw Materials is a part of CMC API Development and consists of 50+ colleagues organized in 4 teams. Your new team consists of 5 colleagues situated in Bagsværd who enjoy social interaction especially expressed through breakfast every Tuesday, walking/running every Wednesday, and a plank challenge almost every week. In CMC Shipping we are dedicated, knowledgeable, indeed knowledge sharing, fun, and open-minded. The position is office based, but we do offer some flexibility by working from home, if the task at hand allows it.
Working at Novo Nordisk
Novo Nordisk 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 Novo Nordisk is working toward something bigger than ourselves, and it's a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 57,000 employees. Together, we go further. Together, we're life changing.
Contact
For further information, please contact Associate Manager,
Marit Klette at +45 3077 6875
Deadline
11th of June 2023
We will review applications and invite for interviews on a continuous basis.
You do not need to write a cover letter, but please write approx. 10-15 lines in your CV about your motivation for the job, highlighting your key skills and contributions to the job. In addition, please avoid the use of photos in your CV. This makes for a better and more fair process. 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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 25.5.2023, 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.
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