28.03.24 | Vollzeit | Köthen (Anhalt) | INDICAL BIOSCIENCE GmbHAnd QM Admin (m/f/d), directly reporting to the Head of Regulatory Affairs and Compliance and being responsible for Preparation of technical documentation in line with product licensures Research and identification of applicable regulations and policies to ensure compliance in line with global growth
Später ansehen28.03.24 | Vollzeit | Köthen (Anhalt) | INDICAL BIOSCIENCE GmbHAnd QM Admin (m/f/d), directly reporting to the Head of Regulatory Affairs and Compliance and being responsible for Preparation of technical documentation in line with product licensures Research and identification of applicable regulations and policies to ensure compliance in line with global growth
Später ansehen28.03.24 | Vollzeit | Köthen (Anhalt) | INDICAL BIOSCIENCE GmbHAnd QM Admin (m/f/d), directly reporting to the Head of Regulatory Affairs and Compliance and being responsible for Preparation of technical documentation in line with product licensures Research and identification of applicable regulations and policies to ensure compliance in line with global growth
Später ansehen28.03.24 | Vollzeit | Köthen (Anhalt) | INDICAL BIOSCIENCE GmbHAnd QM Admin (m/f/d), directly reporting to the Head of Regulatory Affairs and Compliance and being responsible for Preparation of technical documentation in line with product licensures Research and identification of applicable regulations and policies to ensure compliance in line with global growth
Später ansehen28.03.24 | Vollzeit | Köthen (Anhalt) | INDICAL BIOSCIENCE GmbHAnd QM Admin (m/f/d), directly reporting to the Head of Regulatory Affairs and Compliance and being responsible for Preparation of technical documentation in line with product licensures Research and identification of applicable regulations and policies to ensure compliance in line with global growth
Später ansehen28.03.24 | Vollzeit | Köthen (Anhalt) | INDICAL BIOSCIENCE GmbHAnd QM Admin (m/f/d), directly reporting to the Head of Regulatory Affairs and Compliance and being responsible for Preparation of technical documentation in line with product licensures Research and identification of applicable regulations and policies to ensure compliance in line with global growth
Später ansehen14.03.24 | Vollzeit | Bielefeld | Coveris Flexibles Deutschland GmbHPreferably in engineering or technical discipline Willingness to travel approximately 25% of the time time (between Halle-NRW and Rohrdorf (Rosenheim) Quality Management certification of Notified Body 10+ years’ experience in quality and compliance with progressive and extensive experience in medical device
Später ansehen14.03.24 | Vollzeit | Bielefeld | Coveris Flexibles Deutschland GmbHPreferably in engineering or technical discipline Willingness to travel approximately 25% of the time time (between Halle-NRW and Rohrdorf (Rosenheim) Quality Management certification of Notified Body 10+ years’ experience in quality and compliance with progressive and extensive experience in medical device
Später ansehen14.03.24 | Vollzeit | Bielefeld | Coveris Flexibles Deutschland GmbHPreferably in engineering or technical discipline Willingness to travel approximately 25% of the time time (between Halle-NRW and Rohrdorf (Rosenheim) Quality Management certification of Notified Body 10+ years’ experience in quality and compliance with progressive and extensive experience in medical device
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