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Senior Scientific Expert QA Batch Release Support(m/w/x)
Ensuring cGMP compliance for biotherapeutics via lot release documentation review and deviation investigation at a global biopharma leader. 3+ years' GMP experience in pharmaceutical/biotech or regulated industry required. Critical quality assurance function for life-saving therapies.
Anforderungen
- University degree in relevant scientific discipline (Pharmacy, Chemistry, Biology, Biochemistry)
- 3+ years' GMP experience in pharmaceutical/biotech or other regulated industry
- Knowledge of current Good Manufacturing Practices (cGMP) principles
- Knowledge of FDA and EMA requirements
Aufgaben
- Maintain the Quality Assurance System for compliance with company and cGMP standards.
- Maintain the audit program.
- Review functional and release documentation.
- Investigate deviations relevant to your area of responsibility.
- Review lot release documentation.
- Facilitate compliant release processes for the corresponding market.
- Respond to questions from authorities (e.g., Swissmedic, FDA) to ensure timely product release.
- Ensure SOPs are current and align with corporate and regulatory requirements.
- Execute training and awareness related to GMP standards.
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
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Senior Scientific Expert QA Batch Release Support(m/w/x)
Ensuring cGMP compliance for biotherapeutics via lot release documentation review and deviation investigation at a global biopharma leader. 3+ years' GMP experience in pharmaceutical/biotech or regulated industry required. Critical quality assurance function for life-saving therapies.
Anforderungen
- University degree in relevant scientific discipline (Pharmacy, Chemistry, Biology, Biochemistry)
- 3+ years' GMP experience in pharmaceutical/biotech or other regulated industry
- Knowledge of current Good Manufacturing Practices (cGMP) principles
- Knowledge of FDA and EMA requirements
Aufgaben
- Maintain the Quality Assurance System for compliance with company and cGMP standards.
- Maintain the audit program.
- Review functional and release documentation.
- Investigate deviations relevant to your area of responsibility.
- Review lot release documentation.
- Facilitate compliant release processes for the corresponding market.
- Respond to questions from authorities (e.g., Swissmedic, FDA) to ensure timely product release.
- Ensure SOPs are current and align with corporate and regulatory requirements.
- Execute training and awareness related to GMP standards.
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Über das Unternehmen
CSL Behring
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist ein globaler Marktführer in der Biotherapeutik, der innovative Therapien für Patienten mit immunologischen, hämatologischen, kardiovaskulären und anderen Erkrankungen entwickelt.
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