Quality Assurance GMP Jobs in Bad Vilbel
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Suchergebnisse - Quality Assurance GMP Jobs in Bad Vilbel
STADA Arzneimittel AG-Bad Vilbel
für die termingerechte und GMP-konforme Durchführung von Analysen bei externen Partnern
• Du übernimmst den Review und die Freigabe von Analysenergebnissen
• Du stellst die zeitgerechte Erstellung, Bearbeitung und Bewertung von OOS-Ergebnissen sicher
• Du erstellst...
STADA Arzneimittel AG-Bad Vilbel
2001/83/EC
• You possess over 10 years of experience in quality assurance, compliance, and batch release within the pharmaceutical industry
• You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA...
STADA Arzneimittel AG-Bad Vilbel
für die termingerechte und GMP-konforme Durchführung von Analysen bei externen Partnern
• Du übernimmst den Review und die Freigabe von Analysenergebnissen
• Du stellst die zeitgerechte Erstellung, Bearbeitung und Bewertung von OOS-Ergebnissen sicher
• Du erstellst...
STADA Arzneimittel AG-Bad Vilbel
2001/83/EC
• You possess over 10 years of experience in quality assurance, compliance, and batch release within the pharmaceutical industry
• You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA...
STADA Arzneimittel AG-Bad Vilbel
für die termingerechte und GMP-konforme Durchführung von Analysen bei externen Partnern
• Du übernimmst den Review und die Freigabe von Analysenergebnissen
• Du stellst die zeitgerechte Erstellung, Bearbeitung und Bewertung von OOS-Ergebnissen sicher
• Du erstellst...
STADA Arzneimittel AG-Bad Vilbel
2001/83/EC
• You possess over 10 years of experience in quality assurance, compliance, and batch release within the pharmaceutical industry
• You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA...
STADA Arzneimittel AG-Bad Vilbel
instructions and ensure compliance with them
• You determine the required scope of testing and monitor implementation, considering legal frameworks, GMP guidelines, and cost-effectiveness
• You address issues arising from daily operations
• You ensure the...
mindmatch.ai -
STADA Arzneimittel AG-Bad Vilbel
frameworks, GMP guidelines, and cost-effectiveness
• You ensure the necessary training of employees
• You address issues arising from daily operations
• You ensure the implementation of QS-relevant parts of CCPs/MOCs
• You handle deviations and test reports...
STADA Arzneimittel AG-Bad Vilbel
experience in quality assurance, compliance, and batch release within the pharmaceutical industry You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA regulated countries You demonstrate strong leadership...
STADA Arzneimittel AG-Bad Vilbel
instructions and ensure compliance with them
• You determine the required scope of testing and monitor implementation, considering legal frameworks, GMP guidelines, and cost-effectiveness
• You address issues arising from daily operations
• You ensure the...
STADA Arzneimittel AG-Bad Vilbel
2001/83/EC
• You possess over 10 years of experience in quality assurance, compliance, and batch release within the pharmaceutical industry
• You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA...
STADA Arzneimittel AG-Bad Vilbel
2001/83/EC
• You possess over 10 years of experience in quality assurance, compliance, and batch release within the pharmaceutical industry
• You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA...
STADA Arzneimittel AG-Bad Vilbel
2001/83/EC
• You possess over 10 years of experience in quality assurance, compliance, and batch release within the pharmaceutical industry
• You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA...
STADA Arzneimittel AG-Bad Vilbel
2001/83/EC
• You possess over 10 years of experience in quality assurance, compliance, and batch release within the pharmaceutical industry
• You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA...
STADA Arzneimittel AG-Bad Vilbel
2001/83/EC
• You possess over 10 years of experience in quality assurance, compliance, and batch release within the pharmaceutical industry
• You have in-depth knowledge of GMP, GxP, ICH guideline, and global regulatory requirements in EMA and FDA...
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