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Senior Quality Manager for Product Lifecycle Projects(m/w/x)
Quality assurance for medical/pharma products, including GMP specs, supplier qualification, and change control. Solid ISO 13485 knowledge and leadership experience required. Hybrid and flexible working environment.
Anforderungen
- Completed scientific degree in chemistry, pharmacy, or biology, preferably with a doctorate
- Solid knowledge of ISO 13485 and additional regulations in quality and risk management and pharmacy
- Leadership experience
- Experience in project management and knowledge of Lean Quality and quality tools
- Knowledge of production processes and facilities for medical technology or pharmaceutical products under GMP conditions, preferably in the polymer field
- Knowledge of supplier management and auditing experience
- Excellent verbal and written communication skills in German and English
- Strong analytical skills, high problem-solving competence, and strong team orientation
Aufgaben
- Create GMP specifications for raw materials and finished products
- Support the preparation of technical finished product specifications
- Conduct supplier qualifications and qualify external service providers as needed
- Create and track quality assurance agreements with contract manufacturers
- Create and track change control requests
- Support process validation activities
- Review manufacturing instructions and validation documents during method validation
- Prepare quality reviews for products, raw materials, media, and equipment
- Handle deviations, complaints, and CAPA during product introduction
- Provide audit support and manage audits when necessary
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Boni & Prämien
- Performance-based remuneration
Sonstige Vorteile
- Occupational health benefits
Flexibles Arbeiten
- Hybrid working environment
- Flexible working environment
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Senior Quality Manager for Product Lifecycle Projects(m/w/x)
Quality assurance for medical/pharma products, including GMP specs, supplier qualification, and change control. Solid ISO 13485 knowledge and leadership experience required. Hybrid and flexible working environment.
Anforderungen
- Completed scientific degree in chemistry, pharmacy, or biology, preferably with a doctorate
- Solid knowledge of ISO 13485 and additional regulations in quality and risk management and pharmacy
- Leadership experience
- Experience in project management and knowledge of Lean Quality and quality tools
- Knowledge of production processes and facilities for medical technology or pharmaceutical products under GMP conditions, preferably in the polymer field
- Knowledge of supplier management and auditing experience
- Excellent verbal and written communication skills in German and English
- Strong analytical skills, high problem-solving competence, and strong team orientation
Aufgaben
- Create GMP specifications for raw materials and finished products
- Support the preparation of technical finished product specifications
- Conduct supplier qualifications and qualify external service providers as needed
- Create and track quality assurance agreements with contract manufacturers
- Create and track change control requests
- Support process validation activities
- Review manufacturing instructions and validation documents during method validation
- Prepare quality reviews for products, raw materials, media, and equipment
- Handle deviations, complaints, and CAPA during product introduction
- Provide audit support and manage audits when necessary
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Boni & Prämien
- Performance-based remuneration
Sonstige Vorteile
- Occupational health benefits
Flexibles Arbeiten
- Hybrid working environment
- Flexible working environment
Über das Unternehmen
Evonik Operations GmbH
Branche
Other
Beschreibung
Das Unternehmen entwickelt innovative Lösungen für eine nachhaltigere und gesündere Welt.
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- Dr. Franz Köhler Chemie GmbH
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