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:
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:
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.
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