Regulatory Affairs Medical Devices Jobs in Herbrechtingen
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Suchergebnisse - Regulatory Affairs Medical Devices Jobs in Herbrechtingen
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
Affairs role within an international company
• Qualification as PRRC according to MDR
• Comprehensive knowledge of the regulatory requirements of medical device (e.g. MDR, MDD, MPG/MPDG/MPSV, MEDDEV, EN ISO 13485, 21 CFR 820), as well as personal...
PAUL HARTMANN AG-Herbrechtingen
evaluation of product-related regulatory requirements
Qualification:
• University degree in science or technical sciences or an equivalent qualification
• Ideally initial professional experience in the medical device environment or another regulatory field...
PAUL HARTMANN AG-Herbrechtingen
evaluation of product-related regulatory requirements
Qualification:
• University degree in science or technical sciences or an equivalent qualification
• Ideally initial professional experience in the medical device environment or another regulatory field...
PAUL HARTMANN AG-Herbrechtingen
evaluation of product-related regulatory requirements
Qualification:
• University degree in science or technical sciences or an equivalent qualification
• Ideally initial professional experience in the medical device environment or another regulatory field...
PAUL HARTMANN AG-Herbrechtingen
evaluation of product-related regulatory requirements
Qualification:
• University degree in science or technical sciences or an equivalent qualification
• Ideally initial professional experience in the medical device environment or another regulatory field...
PAUL HARTMANN AG-Herbrechtingen
evaluation of product-related regulatory requirements
Qualification:
• University degree in science or technical sciences or an equivalent qualification
• Ideally initial professional experience in the medical device environment or another regulatory field...
PAUL HARTMANN AG-Herbrechtingen
evaluation of product-related regulatory requirements
Qualification:
• University degree in science or technical sciences or an equivalent qualification
• Ideally initial professional experience in the medical device environment or another regulatory field...
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