Qualified Person Delegate - QPD

Category: Quality

Location:Søborg, Capital Region of Denmark, DK

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ensure that all manufacturing activities adhere to relevant regulations and guidelines set forth by regulatory authorities

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review batch records and final release of batch from the CMOs

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set direction and guidance for improve and maintain robust Quality Management Systems to monitor and continuously improve manufacturing processes

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document approval of deviation, change control, and CAPAs to address any issues that may arise during production

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having daily interactions with both internal and external business partners, and while you can expect a high level of complexity in your tasks.

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hold master’s degree in pharmacy, Medicine, Veterinary Medicine, Pharmaceutical chemistry and technology, Chemistry or Biology

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have at least 1 year of experience in a QA related or Process Supporter role

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have gained said experience within the pharmaceutical or medical devices industry

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are fully proficient in English, while Danish knowledge will be seen as an advantage