QA Professional in AM QA Imported Products (1 year maternity cover)

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Do you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in ensuring the quality and safety of our products? If so, there is an exciting job opportunity in Product Supply Aseptic Manufacturing (PS AM) QA which fits perfectly for you. The position
Your key responsibility is, together with your colleagues, to ensure that our documentation is in compliance with internal and external requirements. You will do this by reviewing documents from the production sites along with documentation for the supporting processes such as temperature monitoring etc.
Additionally, you will:
  • Play a central role where you need to make decisions and set directions for Quality. This demands good collaboration skills and a solution-oriented approach when collaborating with colleagues both in the QA organisation but also international colleagues.
  • Have numerous daily encounters with both national and international colleagues, and you can expect a high level of complexity and independent decision making in your daily tasks.
  • Be working closely with your colleagues in an open-plan office and there is on-going sparring in a dynamic and energetic way. Everyone is ready to provide a helping hand if there are challenges with reaching a deadline.
  • We have a positive working environment with a desire and a will to solve challenges through open and honest dialogue. We work together as a team because we ensure collaboration across competences and take care of each other. We always work on improving our way of working and we appreciate new ideas and continues improvements.
    If you are looking for a job which can foster the development of your professional and personal competences, this may be your opportunity. ¬¬ Qualifications
    To be successful in this role, you should have:
  • A Master´s degree in Pharmacy or corresponding education (for example MSc. Chem Eng or MSc. Biology).
  • Ideally, knowledge of GMP, previous experience in QA, batch release, or aseptic production would be advantageous.
  • Passion for quality, problem solving and LEAN methodologies, with a keen interest in acquiring professional competencies and learnings the tricks of the trade.
  • Fluency in both Danish and English.
  • We are seeking a colleague integrates well within the team, both professionally and personally. As a person you are open, honest, forthcoming and inclusive with colleagues in both QA and the production. You thrive in a dynamic environment, taking responsibility and initiative. You are also unafraid to challenge existing processes and are eager to drive your own learning. About the department AM QA Site BA is a department, consisting of approx. 60 dedicated and engaged employees situated in Bagsværd. The department is divided into 4 teams and the open position is in the QA team responsible for release of products imported into EU. Our department ensures a high level of quality in close cooperation with our stakeholders.
    Our responsibility is to assure product quality and regulatory compliance by defining quality requirements, perform quality oversight and by approving quality documents such as procedures, change request and batch- & validation documents. We participate in systematic problem solving and approve deviations. The department is furthermore responsible for assuring the quality of implementation of new equipment and new products in the production facility. 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 to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact
    For further information contact Christina Grebin Rosenkilde +[xxxxx]. Deadline
    23 October 2024.
    Interviews will be held on an ongoing basis
    To ensure an efficient and fair process, please refrain from including a photo of yourself 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 Bagsværd.

    Jobbet er oprettet på vores service den 9.10.2024, 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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    • Bagsværd

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