Dein persönlicher KI-Karriere-Agent
Quality Control Specialist(m/w/x)
Incoming, interim, and final inspections of clinical trial samples, with GMP document preparation. Pharmaceutical quality control experience required. On-site work in a 500+ employee pharmaceutical services provider.
Anforderungen
- Apprenticeship as PTA, PKA, CTA, or Bachelor's in Pharma
- First professional experience in pharmaceutical quality control
- Very good knowledge of GMP/GDP regulatory requirements
- Good knowledge of deviations, CAPAs, and change control
- Good knowledge of IT, ERP, QS systems, and MS Office expertise
- Fluent German and good English skills
- Enjoyment of responsible and meaningful tasks
- Vocational training or Bachelor's degree in relevant fields
- Several years of comparable experience
- First professional experience in QA/QC/production
- Experience in biotech or pharmaceutical industry
- Very good knowledge of GMP/GDP regulatory requirements
- Good knowledge of deviations, CAPAs, and change control
- Good knowledge of IT, ERP, QA systems, and MS Office expertise
- Fluent German and English skills
- Strong self-motivation and team leadership ability
- Enjoyment of responsible and meaningful tasks
Aufgaben
- Conduct incoming goods inspections
- Perform interim and final inspections of clinical trial samples
- Evaluate and document inspection results
- Prepare GMP-relevant documents like SOPs and specifications
- Ensure adherence to GMP procedures
- Support preparation, review, and approval of qualification and validation documents
- Assess batch-specific quality control activities
- Review batch documentation for completeness and GMP compliance
- Support change control measures and implementation
- Conduct root cause analysis and risk assessment
- Examine and evaluate GxP-relevant deviations
- Develop and implement CAPA measures
- Train quality control staff during induction and ongoing training
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – fließend
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office
- IT systems
- ERP systems
- QS data management systems
Noch nicht perfekt?
- PCI Pharma Services Germany GmbHVollzeitnur vor OrtBerufserfahrenGroßbeeren
- ProBioGen AG
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Laborant:in Qualitätskontrolle(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBerlin
Quality Control Specialist(m/w/x)
Incoming, interim, and final inspections of clinical trial samples, with GMP document preparation. Pharmaceutical quality control experience required. On-site work in a 500+ employee pharmaceutical services provider.
Anforderungen
- Apprenticeship as PTA, PKA, CTA, or Bachelor's in Pharma
- First professional experience in pharmaceutical quality control
- Very good knowledge of GMP/GDP regulatory requirements
- Good knowledge of deviations, CAPAs, and change control
- Good knowledge of IT, ERP, QS systems, and MS Office expertise
- Fluent German and good English skills
- Enjoyment of responsible and meaningful tasks
- Vocational training or Bachelor's degree in relevant fields
- Several years of comparable experience
- First professional experience in QA/QC/production
- Experience in biotech or pharmaceutical industry
- Very good knowledge of GMP/GDP regulatory requirements
- Good knowledge of deviations, CAPAs, and change control
- Good knowledge of IT, ERP, QA systems, and MS Office expertise
- Fluent German and English skills
- Strong self-motivation and team leadership ability
- Enjoyment of responsible and meaningful tasks
Aufgaben
- Conduct incoming goods inspections
- Perform interim and final inspections of clinical trial samples
- Evaluate and document inspection results
- Prepare GMP-relevant documents like SOPs and specifications
- Ensure adherence to GMP procedures
- Support preparation, review, and approval of qualification and validation documents
- Assess batch-specific quality control activities
- Review batch documentation for completeness and GMP compliance
- Support change control measures and implementation
- Conduct root cause analysis and risk assessment
- Examine and evaluate GxP-relevant deviations
- Develop and implement CAPA measures
- Train quality control staff during induction and ongoing training
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – fließend
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office
- IT systems
- ERP systems
- QS data management systems
Über das Unternehmen
PCI GER PCI Pharma Services Germany GmbH
Branche
Pharmaceuticals
Beschreibung
The company delivers life-changing therapies and is committed to cultivating an inclusive workplace.
Noch nicht perfekt?
- PCI Pharma Services Germany GmbH
Quality Assurance Specialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenGroßbeeren - ProBioGen AG
QC Scientist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBerlin - PCI GER PCI Pharma Services Germany GmbH
Despatch Quality Control Inspector(m/w/x)
Vollzeitnur vor OrtBerufserfahrenGroßbeeren - LGC Group
Senior QC Scientist(m/w/x)
Vollzeitnur vor OrtSeniorBerlin - LGC Group
Laborant:in Qualitätskontrolle(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBerlin