Dein persönlicher KI-Karriere-Agent
QA Operations Expert(m/w/x)
Release responsible for regulatory compliance, reviewing PQR/APQR documents, and implementing the Manufacturing Manual. 2+ years QA experience in pharma with cGMP and FDA/EMA track record required. Childcare facilities.
Anforderungen
- University Degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology or equivalent
- Professional experience in pharmaceutical industry with direct experience with Pharmaceuticals, Biopharmaceutical or API products and at least 2 years within QA
- Thorough knowledge of cGMP requirements and proven track record with FDA / EMA and other Health Authorities
- Knowledge of GMP and Management of Quality Audits
- Flexibility to work in a fast paced, quickly changing work environment
- Knowledge of Manufacturing Process/ Product Expertise
- Fluent knowledge of English and German (written and spoken)
Aufgaben
- Oversee GxP functions to ensure product quality
- Implement and govern practices from the Novartis Manufacturing Manual
- Act as the release responsible person for regulatory compliance
- Ensure local HA registration and qualified state of facilities
- Review and approve PQR and APQR documents
- Manage exceptions, deviations, and complaints
- Define and implement CAPAs effectively
- Ensure compliance with cGxP and regulatory requirements
- Adhere to HSE guidelines and requirements
- Collaborate in internal and external audits
- Ensure Quality Assurance Agreements with third parties
- Review and approve MBR, specifications, and test methods
- Participate in the compilation and approval of GxP documents
- Support transfer projects and validation studies
- Author SOPs and other GxP documents as needed
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Benefits
Attraktive Vergütung
- Market-competitive base salary
Boni & Prämien
- Attractive incentive program
Betriebliche Altersvorsorge
- Modern company pension scheme
Kinderbetreuung
- Childcare facilities
Weiterbildungsangebote
- Learning and development opportunities
Karriere- und Weiterentwicklung
- Worldwide career possibilities
Noch nicht perfekt?
- Novartis Pharmaceutical Manufacturing GmbHVollzeit/Teilzeitmit HomeofficeBerufserfahrenSchaftenauab 65.605,54 / Jahr
- Novartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenKundlab 58.199,96 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenKundlab 59.781,96 / Jahr - Novartis
QA Compliance Expert(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenSchaftenauab 64.023,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Senior QA Compliance Specialist(m/w/x)
Vollzeit/Teilzeitmit HomeofficeSeniorSchaftenauab 59.781 / Jahr
QA Operations Expert(m/w/x)
Release responsible for regulatory compliance, reviewing PQR/APQR documents, and implementing the Manufacturing Manual. 2+ years QA experience in pharma with cGMP and FDA/EMA track record required. Childcare facilities.
Anforderungen
- University Degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology or equivalent
- Professional experience in pharmaceutical industry with direct experience with Pharmaceuticals, Biopharmaceutical or API products and at least 2 years within QA
- Thorough knowledge of cGMP requirements and proven track record with FDA / EMA and other Health Authorities
- Knowledge of GMP and Management of Quality Audits
- Flexibility to work in a fast paced, quickly changing work environment
- Knowledge of Manufacturing Process/ Product Expertise
- Fluent knowledge of English and German (written and spoken)
Aufgaben
- Oversee GxP functions to ensure product quality
- Implement and govern practices from the Novartis Manufacturing Manual
- Act as the release responsible person for regulatory compliance
- Ensure local HA registration and qualified state of facilities
- Review and approve PQR and APQR documents
- Manage exceptions, deviations, and complaints
- Define and implement CAPAs effectively
- Ensure compliance with cGxP and regulatory requirements
- Adhere to HSE guidelines and requirements
- Collaborate in internal and external audits
- Ensure Quality Assurance Agreements with third parties
- Review and approve MBR, specifications, and test methods
- Participate in the compilation and approval of GxP documents
- Support transfer projects and validation studies
- Author SOPs and other GxP documents as needed
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Benefits
Attraktive Vergütung
- Market-competitive base salary
Boni & Prämien
- Attractive incentive program
Betriebliche Altersvorsorge
- Modern company pension scheme
Kinderbetreuung
- Childcare facilities
Weiterbildungsangebote
- Learning and development opportunities
Karriere- und Weiterentwicklung
- Worldwide career possibilities
Über das Unternehmen
Novartis
Branche
Pharmaceuticals
Beschreibung
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Noch nicht perfekt?
- Novartis Pharmaceutical Manufacturing GmbH
QA Operations Expert(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenSchaftenauab 65.605,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenKundlab 58.199,96 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenKundlab 59.781,96 / Jahr - Novartis
QA Compliance Expert(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenSchaftenauab 64.023,54 / Jahr - Novartis Pharmaceutical Manufacturing GmbH
Senior QA Compliance Specialist(m/w/x)
Vollzeit/Teilzeitmit HomeofficeSeniorSchaftenauab 59.781 / Jahr