Packaging Specialist

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Hillerød

Are you willing to bring your Packaging expertise to support our production capacities globally? Do you have experience with process management and standardization within a GMP regulated environment? Does the challenge of managing worldwide projects and stakeholders excite you? If you would like to join a truly international team, we encourage you to take this rare opportunity and apply for the Packaging Process Specialist position in our Packaging team within our Device Manufacturing Development department. The position As Packaging Process Specialist in Device Manufacturing Development, you will be part of a small team of specialists ensuring that our corporate processes are in compliance with authority requirements and standardized to the extent possible. This includes tasks such as:
  • Updating corporate procedures based on input from stakeholders across all sites globally
  • Implementing new authority requirements via compliance signals
  • Engaging in standardization activities across all sites globally
  • Supporting stakeholders across [xxxxx] with expert knowledge related to the packaging process and [xxxxx] interpretation of requirements
    • In return you can look forward to a rich professional experience with strong collaboration with multiple stakeholders from Corporate to local sites, Research and Development (R&D), Production, Suppliers, Quality Assurance (QA) and other specialists in multiple domains. There would also be some travel opportunities. Qualifications For this role, we are looking forward to connecting with candidates who:
  • Hold at least a Bachelor degree in process engineering, pharmacy or any other relevant field
  • Have a minimum of 5 years of experience in packaging (such as packaging operations, implementation of packaging processes and related equipment, handling authority inspections, for example)
  • Demonstrate expert knowledge within validation and Have a strong quality mindset
  • Possess a proven experience obtained within the pharmaceutical or medical devices industry
  • Are fluent in English (both written and spoken)
    • Who are you as a person? Although we try not to place people in boxes, there are some traits that we believe will help you thrive in this role. You are ideally well organised, someone who never compromises on quality and have a pragmatic approach in your work. An innovative thinker, you are willing to act as lead in our lean activities and to challenge the status quo. Patience, strong communicative aptitudes, and stellar stakeholder management skills will help you deal with the local sites and their practices. It is essential that you are a true team-player at heart: you like to collaborate with colleagues and stakeholders in order to achieve common goals. As a specialist, it is also expected that you will act as a role model for your highly skilled colleagues and that you are ready to support the people around you. About the department You will join Device Manufacturing Development (DMD) and the Packaging department. We are a key function, bridging Packaging R&D to production. We are involved in the development of new products, and responsible for the development and implementation of manufacturing capacity worldwide for new and marketed products. We have an end-to-end presence from product development to production implementation and support. We are engaged in numerous complex and strategic projects for [xxxxx], impacting the company ability to deliver product to the patients, compliance and licence to operate, as well as establishment of the factory of the future globally. Our department located in Hillerød includes 40+ highly engaged skilled professionals from project managers, specialists, validation, process and science experts. We are collaborating with multiple stakeholders. Working at [xxxxx] At [xxxxx], 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, contact Karen Elisabeth Winther at [xxxxx] Deadline 18 April 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 [xxxxx] 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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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Hillerød.

    Jobbet er oprettet på vores service den 4.4.2024, men kan have været deaktiveret og genaktiveret igen.

    Rapportér
    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • 04.04.2024
    • Øvrige
    • Hillerød
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