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Johnson & Johnson Vor 8 Tagen

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 ...years of related experience, including significant experience working in pharmaceutical, medical device or other related or highly regulated industry with prior experience with completion of manufacturing/packaging investigation and/or MDR process (in Medical Device and/...  >>

Synbias Pharma AG Vor 15 Tagen

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 ...discipline or equivalent. Zero to two (0-2) years of relevant experience in documentation, QA or equivalent. Knowledge of GMP regulations and GDP preferred. Detail oriented and strong written and verbal communication skills. Ability to work independently, within...  >>

Vor 12 Stunden

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 ...driven, Excellent social skills, Team player, Able and willing to work in a complex organization with highly detailed rules and regulations, Computer literate * Able to work in a global organisation. * Some flexibility in working hours is required, Must be able to...  >>

Vor 18 Tagen

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 ...Technical Profile Requirements: * Must be able to lead and give direction to Validation Projects. * Minimum of 2 years working in a regulated environment, a minimum 1 of which has been spent carrying out validation activities. * English and German spoken and written....  >>

Vor 7 Tagen

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 ...suppliers in product life cycle management projects. * Support to ensure the design transfer is performed according to the QMS regulation. * Pragmatic but compliant application of the PLCM process. * Ensuring the Risk Management process is followed. * Improvement...  >>

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