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GMP Supporter and Pest Control responsible (Denmark, Hillerød)

Novo Nordisk A/S



Jobbeskrivelse
Placering
Hillerød, Denmark

Jobkategori
Engineering & Technical

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Are you someone who thrives on challenges and can handle multiple tasks simultaneously? Do you possess a creative mindset that enables you to think outside the box and find optimal solutions? Are you capable of taking ownership and influencing the approach to quality? Do you excel at analyzing and working with data, presenting and communicating your ideas effectively, and building consensus around them? If so, we invite you to apply for the position of Good Manufacturing Practice (GMP) Supporter, as we work towards transforming our factory into the "Factory of the Future".

Apply today and join us for a life-changing career!

The Position
The job of a GMP supporter is extremely varied. You will work with operators, supporters, QA, and other departments to implement improvements and new initiatives. Collaboration takes place in a dynamic and fast-paced environment, providing you with a great opportunity to influence your daily work through teamwork and independent efforts.

The tasks include, but are not limited to:

  • Setting the course for general GMP work in collaboration with management and GMP coordinators.
  • Working with deviations, conducting systematic problem-solving, and finding solutions to newly discovered challenges.
  • Coaching and assisting colleagues in GMP-related tasks such as deviations, changes, projects, etc.
  • Managing and documenting processes through SOPs, other critical documentation, and training materials.
  • Manage the facility's pest control program, including coordinating with external vendors, conducting inspections, and implementing control measures to prevent infestations.
  • Provide training and support to employees on pest control best practices.

Qualifications
We're seeking candidates who fulfil the following prerequisites:

  • You may possess a technical background, such as an AP Graduate or a similar qualification.
  • Preferable at least 3 years of experience in GMP-regulated production.
  • Experience in data analysis and a desire to develop procedures and processes.
  • A LEAN mindset with experience in systematic problem-solving.
  • Proficient in both Danish and English, communicating and writing.

As a person you are a proactive and methodical individual, always willing to take the initiative to solve challenges. Your focus is not only on supporting stakeholders but also on improving overall quality. You possess excellent interpersonal skills and are adept at gaining support and building consensus for our projects. Additionally, you have a strong interest in becoming an advocate for quality mindset, making you a suitable candidate for the position.

About the Department
Our Facility Team consists of 18 dedicated individuals with a very diverse and comprehensive portfolio of tasks and areas of responsibility and very diverse profiles as well as backgrounds. We have a safe and forthcoming atmosphere in the office and we strive to communicate and coordinate to increase transparency and effectiveness. We support a complex and dynamic production in both 25A and 25B ensuring amongst other things compliance with regulatory requirements and assist in optimizing processes and provide supportive framework together with the rest of Production Support.

Working at Novo Nordisk
At Novo Nordisk, 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 Thomas Feldborg on +45 3448 2919 on Fridays between 13:00 and 16:00.

Deadline
Apply before November, 15 2024.

Interviews will be conducted on an ongoing basis, so we encourage you to apply as soon as possible.

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 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.

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Ansøgningsfrist d. 15.11.2024
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Novo Nordisk A/S

Novo Allé, 2880 Bagsværd

Novo Nordisk is a global healthcare company with more than 90 years of innovation and leadership in diabetes care. This heritage has given us experience and capabilities that also enable us to help people defeat other serious chronic conditions: haemophilia, growth disorders and obesity.

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