Your personal AI career 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.
Requirements
- 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
Tasks
- 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
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Native
- English – Business Fluent
Tools & Technologies
- MS Office
- IT systems
- ERP systems
- QS data management systems
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
Not a perfect match?
- PCI GER PCI Pharma Services Germany GmbHFull-timeOn-siteExperiencedGroßbeeren
- PCI Pharma Services Germany GmbH
Quality Assurance Specialist(m/w/x)
Full-timeOn-siteExperiencedGroßbeeren - ProBioGen AG
QC Scientist(m/w/x)
Full-timeOn-siteExperiencedBerlin - LGC Group
Laborant:in Qualitätskontrolle(m/w/x)
Full-timeOn-siteExperiencedBerlin - LGC
QC Scientist(m/w/x)
Full-timeOn-siteExperiencedBerlin
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.
Requirements
- 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
Tasks
- 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
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Native
- English – Business Fluent
Tools & Technologies
- MS Office
- IT systems
- ERP systems
- QS data management systems
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
PCI GER PCI Pharma Services Germany GmbH
Industry
Pharmaceuticals
Description
The company delivers life-changing therapies and is committed to cultivating an inclusive workplace.
Not a perfect match?
- PCI GER PCI Pharma Services Germany GmbH
Despatch Quality Control Inspector(m/w/x)
Full-timeOn-siteExperiencedGroßbeeren - PCI Pharma Services Germany GmbH
Quality Assurance Specialist(m/w/x)
Full-timeOn-siteExperiencedGroßbeeren - ProBioGen AG
QC Scientist(m/w/x)
Full-timeOn-siteExperiencedBerlin - LGC Group
Laborant:in Qualitätskontrolle(m/w/x)
Full-timeOn-siteExperiencedBerlin - LGC
QC Scientist(m/w/x)
Full-timeOn-siteExperiencedBerlin