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        • Darmstadt, Hessen
        • Arbeitnehmerüberlassung
        • €4,602 - €6,339 pro monat
        • Vollzeit
        Founded in Amsterdam in 1960, the globally active Randstad Group has been both a strategic partner for companies and an attractive employer for qualified employees for decades. We are currently looking for a CMC Expert for our customer, a pharmaceutical company in Darmstadt. Trust in our experience and our long-standing contacts with personnel decision-makers.Das dürfen Sie erwartenPerformance-related pay in accordance with the BAP/DGB collective agreement and increasing income through sectoral bonuses in the chemical industryRepresentation by a nationwide general works councilPreventive health care through our company medical centre - free services in all aspects of occupational medicine and individual answers to your health questionsUp to 30 days holiday per yearAs a rule, an employment contract of indefinite durationIntegration of severely disabled candidatesIhre AufgabenWork in close cooperation with interdisciplinary CMC project teams and the entire Global Regulatory Affairs functionActively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learnedEstablish and maintain sound working relationships with partners and customersContribute to the Global regulatory strategy for the assigned products in target regions/countriesAssist senior colleagues for the global CMC strategy and plan for dossiers related to the assigned project/productsAnswer to Health Authority queries, life cycle management submissions, marketing authorization applications, briefing documentation for Health Authority interactionsResponsible to provide country specific CMC regulatory requirements for dossier strategies and plans in close collaboration with other GRA functionsReview relevant technical documents intended for the products documentation platform or for local submission to confirm alignment of the report conclusions with the CMC Dossier Strategy and PlanSupport to confirm alignment between CMC dossier strategy and CMC regulatory documents before approval regarding fit to strategy, gaps, issues, risks and mitigation measures (within Dossier Generation Team)Accountable to track submission and approval status to ensure regulatory compliance for all CMC dossier submissions worldwideSupport development and execute initiatives to ensure regulatory compliance - as requiredUnsere AnforderungenDegree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalentAdvanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent is an assetPrior experience in regulatory affairs CMC/Module 3Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology in small moleculesExperience of regulations, guidelines for NCEs and product life cycle maintenance Corona virus and application at Randstad: Our application process supports our motto „human forward“. In the current situation it is most important to fulfill our social responsibility and to preserve the health of our applicants and employees at the same time. Therefore our application process can be carried out completey contact-free. You can still apply online, we’re looking forward to hear from you!
        Founded in Amsterdam in 1960, the globally active Randstad Group has been both a strategic partner for companies and an attractive employer for qualified employees for decades. We are currently looking for a CMC Expert for our customer, a pharmaceutical company in Darmstadt. Trust in our experience and our long-standing contacts with personnel decision-makers.Das dürfen Sie erwartenPerformance-related pay in accordance with the BAP/DGB collective agreement and increasing income through sectoral bonuses in the chemical industryRepresentation by a nationwide general works councilPreventive health care through our company medical centre - free services in all aspects of occupational medicine and individual answers to your health questionsUp to 30 days holiday per yearAs a rule, an employment contract of indefinite durationIntegration of severely disabled candidatesIhre AufgabenWork in close cooperation with interdisciplinary CMC project teams and the entire Global Regulatory Affairs functionActively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learnedEstablish and maintain sound working relationships with partners and customersContribute to the Global regulatory strategy for the assigned products in target regions/countriesAssist senior colleagues for the global CMC strategy and plan for dossiers related to the assigned project/productsAnswer to Health Authority queries, life cycle management submissions, marketing authorization applications, briefing documentation for Health Authority interactionsResponsible to provide country specific CMC regulatory requirements for dossier strategies and plans in close collaboration with other GRA functionsReview relevant technical documents intended for the products documentation platform or for local submission to confirm alignment of the report conclusions with the CMC Dossier Strategy and PlanSupport to confirm alignment between CMC dossier strategy and CMC regulatory documents before approval regarding fit to strategy, gaps, issues, risks and mitigation measures (within Dossier Generation Team)Accountable to track submission and approval status to ensure regulatory compliance for all CMC dossier submissions worldwideSupport development and execute initiatives to ensure regulatory compliance - as requiredUnsere AnforderungenDegree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalentAdvanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent is an assetPrior experience in regulatory affairs CMC/Module 3Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology in small moleculesExperience of regulations, guidelines for NCEs and product life cycle maintenance Corona virus and application at Randstad: Our application process supports our motto „human forward“. In the current situation it is most important to fulfill our social responsibility and to preserve the health of our applicants and employees at the same time. Therefore our application process can be carried out completey contact-free. You can still apply online, we’re looking forward to hear from you!
        • Darmstadt, Hessen
        • Arbeitnehmerüberlassung
        • €5,500 - €6,000 pro monat
        • Vollzeit
        Founded in Amsterdam in 1960, the globally active Randstad Group has been both a strategic partner for companies and an attractive employer for qualified employees for decades. We are currently looking for a study director for safety pharmacology studies for our customer, a pharmaceutical company in Darmstadt. Trust in our experience and our long-standing contacts with personnel decision-makers.Das dürfen Sie erwartenPerformance-related pay in accordance with the BAP/DGB collective agreement and increasing income through sectoral bonuses in the chemical industryRepresentation by a nationwide general works councilPreventive health care through our company medical centre - free services in all aspects of occupational medicine and individual answers to your health questionsUp to 30 days holiday per yearAs a rule, an employment contract of indefinite durationIhre AufgabenMember of the Preclinical Chemical & Safety (CPS) functionEnsure that the required preclinical safety studies for characterization of new chemical or biological entities are designed, conducted and reported in time and meet national and international requirementsPresent preclinical safety data or toxicological assessments to internal teamsRepresent CPS in internal and external groups and act as multilateral interface between the different functions within the R&D organizationScientific networking with internal and external experts Unsere AnforderungenPhD degree in safety pharmacology, veterinary medicine or biology with 1 to 3 years of experience in pharmaceutical industrySpecific expertise in physiology / pathophysiology and preclinical in-vivo safety testingExpertise in imaging technologies are desiredTeam working abilitiesBackground in developing pharma products (oncology/immunology/immunoncology)Good knowledge of guidelines in regulatory safety pharmacology, GLP and animal welfare regulationsGood communication skillsFluent in English Corona virus and application at Randstad: Our application process supports our motto „human forward“. In the current situation it is most important to fulfill our social responsibility and to preserve the health of our applicants and employees at the same time. Therefore our application process can be carried out completey contact-free. You can still apply online, we’re looking forward to hear from you!
        Founded in Amsterdam in 1960, the globally active Randstad Group has been both a strategic partner for companies and an attractive employer for qualified employees for decades. We are currently looking for a study director for safety pharmacology studies for our customer, a pharmaceutical company in Darmstadt. Trust in our experience and our long-standing contacts with personnel decision-makers.Das dürfen Sie erwartenPerformance-related pay in accordance with the BAP/DGB collective agreement and increasing income through sectoral bonuses in the chemical industryRepresentation by a nationwide general works councilPreventive health care through our company medical centre - free services in all aspects of occupational medicine and individual answers to your health questionsUp to 30 days holiday per yearAs a rule, an employment contract of indefinite durationIhre AufgabenMember of the Preclinical Chemical & Safety (CPS) functionEnsure that the required preclinical safety studies for characterization of new chemical or biological entities are designed, conducted and reported in time and meet national and international requirementsPresent preclinical safety data or toxicological assessments to internal teamsRepresent CPS in internal and external groups and act as multilateral interface between the different functions within the R&D organizationScientific networking with internal and external experts Unsere AnforderungenPhD degree in safety pharmacology, veterinary medicine or biology with 1 to 3 years of experience in pharmaceutical industrySpecific expertise in physiology / pathophysiology and preclinical in-vivo safety testingExpertise in imaging technologies are desiredTeam working abilitiesBackground in developing pharma products (oncology/immunology/immunoncology)Good knowledge of guidelines in regulatory safety pharmacology, GLP and animal welfare regulationsGood communication skillsFluent in English Corona virus and application at Randstad: Our application process supports our motto „human forward“. In the current situation it is most important to fulfill our social responsibility and to preserve the health of our applicants and employees at the same time. Therefore our application process can be carried out completey contact-free. You can still apply online, we’re looking forward to hear from you!
        • Darmstadt, Hessen
        • Arbeitnehmerüberlassung
        • €3,300 - €3,800 pro monat
        • Vollzeit
        Zeit für Veränderungen - Zeit für einen neuen Job! Sie sind CTA oder PTA und auf der Suche nach einer neuen beruflichen Herausforderung in Darmstadt? Wir haben, was Sie suchen: Einen sicheren Arbeitsplatz, attraktive Benefits und einen Job mit spannenden Aufgaben bei unserem Kunden aus der Pharmabranche.Das dürfen Sie erwartenLeistungsgerechte, übertarifliche Vergütung auf Basis des Tarifvertrages BAP/DGBUmfangreiche Sozialleistungen, inklusive Weihnachts- und UrlaubsgeldZuschuss zur betrieblichen Altersvorsorge nach ProbezeitendeInteressensvertretung durch einen flächendeckenden Betriebsrat250 € Prämie für jeden Mitarbeiter, den Sie erfolgreich für uns werbenUrlaubsanträge, Entgeltnachweise und Informationen des Betriebsrates per AppIhre AufgabenImplementierung eines neuen CDSMitarbeit bei der Definition der neuen Abläufe und Abstimmung dieser mit den betroffenen BereichenBeteiligt an der Konzeptionierung und Erstellung der CDS-Stammdaten und Methoden, inkl. Aufsetzen und Validierung von analytischen BerechnungenPlanung, Bearbeitung und Durchführung der Validierung des CDS nach globalen VorgabenSOPs erstellen und bei der Erstellung der Validierungsdokumente mitarbeitenUnsere AnforderungenNaturwissenschaftlicher Hintergrund (z.B. Chemie, Pharmazie etc.)Erfahrung in pharmazeutischen Qualitätskontrolllaboren von VorteilOrganisationsfähigkeit, Zuverlässigkeit, Sorgfalt, Verantwortungsgefühl und TeamfähigkeitGrundkenntnisse in der Validierung elektronischer Systeme und Kenntnisse der cGMP-VorgabenEDV-Kenntnisse (MS Office, CDS - vorzugsweise Empower)Gute Englischkenntnisse in Wort und Schrift  Als Tochter der 1960 in Amsterdam gegründeten Randstad N.V. ist Randstad Deutschlands Personaldienstleister Nr. 1 und Garant für Kompetenz und Sicherheit. Aber für uns zählt nicht nur Größe: Was uns in den über 550 Niederlassungen in Deutschland antreibt, ist der Erfolg unserer Kunden und Kandidaten.Unsere Marke ist ein Versprechen: Für unsere Kunden und Mitarbeiter stehen wir für unseren Anspruch, gemeinsam weiterzukommen - auf menschliche Art. Das nennen wir: Human Forward - Zwei Wörter, die sagen, wer wir sind, woran wir glauben und wofür wir stehen.Wir sind der vertrauenswürdige und persönliche Partner in der von Technologie geprägten Welt der Arbeit. Wir helfen Unternehmen und Bewerbern dabei, ihr wahres Potenzial auszuschöpfen. Mit intelligenter Technologie – aber zugleich ganz persönlich. Denn wir wissen aus Erfahrung, dass echte Verbindungen nicht aus Daten und Algorithmen entstehen – sie brauchen menschliche Interaktion, Empathie und Intuition.Überzeugen Sie sich selbst und bewerben Sie sich jetzt direkt online! Bewerbungen schwerbehinderter Menschen sind uns selbstverständlich willkommen.Corona Virus und Bewerbung bei Randstad: Unser Bewerbungsprozess unterstützt unser "Human Forward"-Versprechen. Das bedeutet aktuell: Persönliche Kontakte vermeiden, da für uns die Gesundheit unserer Kandidaten und Mitarbeiter und unsere gemeinsame gesellschaftliche Verantwortung höchste Priorität haben. Daher ist unser Bewerbungsprozess auch vollständig ohne direkten und persönlichen Kontakt weiterhin möglich. Bitte bewerben Sie sich gerne weiterhin online, wir freuen uns auf Sie.
        Zeit für Veränderungen - Zeit für einen neuen Job! Sie sind CTA oder PTA und auf der Suche nach einer neuen beruflichen Herausforderung in Darmstadt? Wir haben, was Sie suchen: Einen sicheren Arbeitsplatz, attraktive Benefits und einen Job mit spannenden Aufgaben bei unserem Kunden aus der Pharmabranche.Das dürfen Sie erwartenLeistungsgerechte, übertarifliche Vergütung auf Basis des Tarifvertrages BAP/DGBUmfangreiche Sozialleistungen, inklusive Weihnachts- und UrlaubsgeldZuschuss zur betrieblichen Altersvorsorge nach ProbezeitendeInteressensvertretung durch einen flächendeckenden Betriebsrat250 € Prämie für jeden Mitarbeiter, den Sie erfolgreich für uns werbenUrlaubsanträge, Entgeltnachweise und Informationen des Betriebsrates per AppIhre AufgabenImplementierung eines neuen CDSMitarbeit bei der Definition der neuen Abläufe und Abstimmung dieser mit den betroffenen BereichenBeteiligt an der Konzeptionierung und Erstellung der CDS-Stammdaten und Methoden, inkl. Aufsetzen und Validierung von analytischen BerechnungenPlanung, Bearbeitung und Durchführung der Validierung des CDS nach globalen VorgabenSOPs erstellen und bei der Erstellung der Validierungsdokumente mitarbeitenUnsere AnforderungenNaturwissenschaftlicher Hintergrund (z.B. Chemie, Pharmazie etc.)Erfahrung in pharmazeutischen Qualitätskontrolllaboren von VorteilOrganisationsfähigkeit, Zuverlässigkeit, Sorgfalt, Verantwortungsgefühl und TeamfähigkeitGrundkenntnisse in der Validierung elektronischer Systeme und Kenntnisse der cGMP-VorgabenEDV-Kenntnisse (MS Office, CDS - vorzugsweise Empower)Gute Englischkenntnisse in Wort und Schrift  Als Tochter der 1960 in Amsterdam gegründeten Randstad N.V. ist Randstad Deutschlands Personaldienstleister Nr. 1 und Garant für Kompetenz und Sicherheit. Aber für uns zählt nicht nur Größe: Was uns in den über 550 Niederlassungen in Deutschland antreibt, ist der Erfolg unserer Kunden und Kandidaten.Unsere Marke ist ein Versprechen: Für unsere Kunden und Mitarbeiter stehen wir für unseren Anspruch, gemeinsam weiterzukommen - auf menschliche Art. Das nennen wir: Human Forward - Zwei Wörter, die sagen, wer wir sind, woran wir glauben und wofür wir stehen.Wir sind der vertrauenswürdige und persönliche Partner in der von Technologie geprägten Welt der Arbeit. Wir helfen Unternehmen und Bewerbern dabei, ihr wahres Potenzial auszuschöpfen. Mit intelligenter Technologie – aber zugleich ganz persönlich. Denn wir wissen aus Erfahrung, dass echte Verbindungen nicht aus Daten und Algorithmen entstehen – sie brauchen menschliche Interaktion, Empathie und Intuition.Überzeugen Sie sich selbst und bewerben Sie sich jetzt direkt online! Bewerbungen schwerbehinderter Menschen sind uns selbstverständlich willkommen.Corona Virus und Bewerbung bei Randstad: Unser Bewerbungsprozess unterstützt unser "Human Forward"-Versprechen. Das bedeutet aktuell: Persönliche Kontakte vermeiden, da für uns die Gesundheit unserer Kandidaten und Mitarbeiter und unsere gemeinsame gesellschaftliche Verantwortung höchste Priorität haben. Daher ist unser Bewerbungsprozess auch vollständig ohne direkten und persönlichen Kontakt weiterhin möglich. Bitte bewerben Sie sich gerne weiterhin online, wir freuen uns auf Sie.
        • Darmstadt, Hessen
        • Arbeitnehmerüberlassung
        • €5,500 - €6,000 pro monat
        • Vollzeit
        Founded in Amsterdam in 1960, the globally active Randstad Group has been both a strategic partner for companies and an attractive employer for qualified employees for decades. We are currently looking for a study director for safety pharmacology studies for our customer, a pharmaceutical company in Darmstadt. Trust in our experience and our long-standing contacts with personnel decision-makers.Das dürfen Sie erwartenPerformance-related pay in accordance with the BAP/DGB collective agreement and increasing income through sectoral bonuses in the chemical industryRepresentation by a nationwide general works councilPreventive health care through our company medical centre - free services in all aspects of occupational medicine and individual answers to your health questionsUp to 30 days holiday per yearAs a rule, an employment contract of indefinite durationIhre AufgabenMember of the Preclinical Chemical & Safety (CPS) functionEnsure that the required preclinical safety studies for characterization of new chemical or biological entities are designed, conducted and reported in time and meet national and international requirementsPresent preclinical safety data or toxicological assessments to internal teamsRepresent CPS in internal and external groups and act as multilateral interface between the different functions within the R&D organizationScientific networking with internal and external experts Unsere AnforderungenPhD degree in safety pharmacology, veterinary medicine or biology with 1 to 3 years of experience in pharmaceutical industrySpecific expertise in physiology / pathophysiology and preclinical in-vivo safety testingExpertise in imaging technologies are desiredTeam working abilitiesBackground in developing pharma products (oncology/immunology/immunoncology)Good knowledge of guidelines in regulatory safety pharmacology, GLP and animal welfare regulationsGood communication skillsFluent in English Corona virus and application at Randstad: Our application process supports our motto „human forward“. In the current situation it is most important to fulfill our social responsibility and to preserve the health of our applicants and employees at the same time. Therefore our application process can be carried out completey contact-free. You can still apply online, we’re looking forward to hear from you!
        Founded in Amsterdam in 1960, the globally active Randstad Group has been both a strategic partner for companies and an attractive employer for qualified employees for decades. We are currently looking for a study director for safety pharmacology studies for our customer, a pharmaceutical company in Darmstadt. Trust in our experience and our long-standing contacts with personnel decision-makers.Das dürfen Sie erwartenPerformance-related pay in accordance with the BAP/DGB collective agreement and increasing income through sectoral bonuses in the chemical industryRepresentation by a nationwide general works councilPreventive health care through our company medical centre - free services in all aspects of occupational medicine and individual answers to your health questionsUp to 30 days holiday per yearAs a rule, an employment contract of indefinite durationIhre AufgabenMember of the Preclinical Chemical & Safety (CPS) functionEnsure that the required preclinical safety studies for characterization of new chemical or biological entities are designed, conducted and reported in time and meet national and international requirementsPresent preclinical safety data or toxicological assessments to internal teamsRepresent CPS in internal and external groups and act as multilateral interface between the different functions within the R&D organizationScientific networking with internal and external experts Unsere AnforderungenPhD degree in safety pharmacology, veterinary medicine or biology with 1 to 3 years of experience in pharmaceutical industrySpecific expertise in physiology / pathophysiology and preclinical in-vivo safety testingExpertise in imaging technologies are desiredTeam working abilitiesBackground in developing pharma products (oncology/immunology/immunoncology)Good knowledge of guidelines in regulatory safety pharmacology, GLP and animal welfare regulationsGood communication skillsFluent in English Corona virus and application at Randstad: Our application process supports our motto „human forward“. In the current situation it is most important to fulfill our social responsibility and to preserve the health of our applicants and employees at the same time. Therefore our application process can be carried out completey contact-free. You can still apply online, we’re looking forward to hear from you!
        • Darmstadt, Hessen
        • Arbeitnehmerüberlassung
        • €4,602 - €6,339 pro monat
        • Vollzeit
        Founded in Amsterdam in 1960, the globally active Randstad Group has been both a strategic partner for companies and an attractive employer for qualified employees for decades. We are currently looking for a CMC Expert for our customer, a pharmaceutical company in Darmstadt. Trust in our experience and our long-standing contacts with personnel decision-makers.Das dürfen Sie erwartenPerformance-related pay in accordance with the BAP/DGB collective agreement and increasing income through sectoral bonuses in the chemical industryRepresentation by a nationwide general works councilPreventive health care through our company medical centre - free services in all aspects of occupational medicine and individual answers to your health questionsUp to 30 days holiday per yearAs a rule, an employment contract of indefinite durationIntegration of severely disabled candidatesIhre AufgabenWork in close cooperation with interdisciplinary CMC project teams and the entire Global Regulatory Affairs functionActively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learnedEstablish and maintain sound working relationships with partners and customersContribute to the Global regulatory strategy for the assigned products in target regions/countriesAssist senior colleagues for the global CMC strategy and plan for dossiers related to the assigned project/productsAnswer to Health Authority queries, life cycle management submissions, marketing authorization applications, briefing documentation for Health Authority interactionsResponsible to provide country specific CMC regulatory requirements for dossier strategies and plans in close collaboration with other GRA functionsReview relevant technical documents intended for the products documentation platform or for local submission to confirm alignment of the report conclusions with the CMC Dossier Strategy and PlanSupport to confirm alignment between CMC dossier strategy and CMC regulatory documents before approval regarding fit to strategy, gaps, issues, risks and mitigation measures (within Dossier Generation Team)Accountable to track submission and approval status to ensure regulatory compliance for all CMC dossier submissions worldwideSupport development and execute initiatives to ensure regulatory compliance - as requiredUnsere AnforderungenDegree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalentAdvanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent is an assetPrior experience in regulatory affairs CMC/Module 3Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology in small moleculesExperience of regulations, guidelines for NCEs and product life cycle maintenance Corona virus and application at Randstad: Our application process supports our motto „human forward“. In the current situation it is most important to fulfill our social responsibility and to preserve the health of our applicants and employees at the same time. Therefore our application process can be carried out completey contact-free. You can still apply online, we’re looking forward to hear from you!
        Founded in Amsterdam in 1960, the globally active Randstad Group has been both a strategic partner for companies and an attractive employer for qualified employees for decades. We are currently looking for a CMC Expert for our customer, a pharmaceutical company in Darmstadt. Trust in our experience and our long-standing contacts with personnel decision-makers.Das dürfen Sie erwartenPerformance-related pay in accordance with the BAP/DGB collective agreement and increasing income through sectoral bonuses in the chemical industryRepresentation by a nationwide general works councilPreventive health care through our company medical centre - free services in all aspects of occupational medicine and individual answers to your health questionsUp to 30 days holiday per yearAs a rule, an employment contract of indefinite durationIntegration of severely disabled candidatesIhre AufgabenWork in close cooperation with interdisciplinary CMC project teams and the entire Global Regulatory Affairs functionActively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learnedEstablish and maintain sound working relationships with partners and customersContribute to the Global regulatory strategy for the assigned products in target regions/countriesAssist senior colleagues for the global CMC strategy and plan for dossiers related to the assigned project/productsAnswer to Health Authority queries, life cycle management submissions, marketing authorization applications, briefing documentation for Health Authority interactionsResponsible to provide country specific CMC regulatory requirements for dossier strategies and plans in close collaboration with other GRA functionsReview relevant technical documents intended for the products documentation platform or for local submission to confirm alignment of the report conclusions with the CMC Dossier Strategy and PlanSupport to confirm alignment between CMC dossier strategy and CMC regulatory documents before approval regarding fit to strategy, gaps, issues, risks and mitigation measures (within Dossier Generation Team)Accountable to track submission and approval status to ensure regulatory compliance for all CMC dossier submissions worldwideSupport development and execute initiatives to ensure regulatory compliance - as requiredUnsere AnforderungenDegree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalentAdvanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent is an assetPrior experience in regulatory affairs CMC/Module 3Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology in small moleculesExperience of regulations, guidelines for NCEs and product life cycle maintenance Corona virus and application at Randstad: Our application process supports our motto „human forward“. In the current situation it is most important to fulfill our social responsibility and to preserve the health of our applicants and employees at the same time. Therefore our application process can be carried out completey contact-free. You can still apply online, we’re looking forward to hear from you!

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