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GMP Compliance Specialist(m/w/x)
Managing local GMP compliance and quality risk activities for synthetic/large molecule manufacturing. Experience in synthetic/large molecule manufacturing and QC required. Work at 100,000+ employee global pharma.
Anforderungen
- Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, or equivalent
- Experience in synthetic and/or large molecule manufacturing and quality control
- Flexibility and teamwork skills
- Curiosity about team priorities and workload
- Empowerment to make decisions and ownership of work
- Seeking feedback for continuous improvement
- Excellent language skills, fluent in German and good communication in English
Aufgaben
- Manage local GMP compliance processes
- Coordinate quality risk management activities
- Facilitate handling of deviations and CAPA
- Support changes in GMP compliance
- Act as an expert for quality systems
- Provide first-level support for business processes
- Train subject matter experts on quality systems
- Manage access to GMP relevant areas
- Oversee account management for GMP systems
- Handle inspection management for internal audits
- Prepare for health authority inspections
- Drive optimization of GMP-related processes
- Standardize the existing document landscape
- Collaborate with team members in a role-based environment
- Build relationships with customers and partners
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – fließend
- Englisch – verhandlungssicher
Noch nicht perfekt?
- Roche Pharma AGVollzeitBefristeter Vertragnur vor OrtBerufserfahrenGrenzach
- Roche
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GMP Compliance Specialist(m/w/x)
Managing local GMP compliance and quality risk activities for synthetic/large molecule manufacturing. Experience in synthetic/large molecule manufacturing and QC required. Work at 100,000+ employee global pharma.
Anforderungen
- Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, or equivalent
- Experience in synthetic and/or large molecule manufacturing and quality control
- Flexibility and teamwork skills
- Curiosity about team priorities and workload
- Empowerment to make decisions and ownership of work
- Seeking feedback for continuous improvement
- Excellent language skills, fluent in German and good communication in English
Aufgaben
- Manage local GMP compliance processes
- Coordinate quality risk management activities
- Facilitate handling of deviations and CAPA
- Support changes in GMP compliance
- Act as an expert for quality systems
- Provide first-level support for business processes
- Train subject matter experts on quality systems
- Manage access to GMP relevant areas
- Oversee account management for GMP systems
- Handle inspection management for internal audits
- Prepare for health authority inspections
- Drive optimization of GMP-related processes
- Standardize the existing document landscape
- Collaborate with team members in a role-based environment
- Build relationships with customers and partners
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – fließend
- Englisch – verhandlungssicher
Über das Unternehmen
1201 F. Hoffmann-La Roche AG
Branche
Pharmaceuticals
Beschreibung
Roche is dedicated to advancing science and ensuring access to healthcare for everyone, with over 100,000 employees globally.
Noch nicht perfekt?
- Roche Pharma AG
QA Manager für das Quality System und Compliance in Central Certification(m/w/x)
VollzeitBefristeter Vertragnur vor OrtBerufserfahrenGrenzach - Roche
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Vollzeitnur vor OrtSeniorKaiseraugst - 1201 F. Hoffmann-La Roche AG
QC Investigator(m/w/x)
Vollzeitnur vor OrtBerufserfahrenKaiseraugst - 1201 F. Hoffmann-La Roche AG
QA Manager IT/OT(m/w/x)
Vollzeitnur vor OrtSeniorBasel