In keeping with this strategy we are offering an exciting opportunity for the position of a Regional Quality Manager (m/f/x). The Regional Quality Manager's mission is to lead the Quality and Regulatory Assurance strategy across MLEMEA taking a leadership role in developing and implementing the regional strategy and priorities.
To strengthen the Fonterra Europe organisation, we are looking for an experienced and motivated Head of Food Safety, Quality and Regulatory, to maintain Fonterra’s high standards. POSITION Responsible for leading and driving Food Safety, Quality and Regulatory strategic focusses and culture to ensure success of Fonterra’s strategic objectives Managing a team of professionals, 3 direct and 4 indirect reports, and supporting and further developing an inclusive and high performance culture Ensuring the Food Safety & Quality priorities and resources are aligned with business needs, working closely together with a.o.
Freizeitausgleich Nach Möglichkeit Arbeiten aus dem Homeoffice Individuelle Betreuung durch Ihre/n persönliche/n CENIS AnsprechpartnerIn „MitarbeiterInnen-werben-MitarbeiterInnen-Prämie“ in Höhe von bis zu 1.500 Euro Starten Sie mit uns durch und übernehmen Sie gerne Verantwortung in der unten beschriebenen Position. / Take the next step in your career and take on responsibility in the position described below. Start as a Quality Engineer (m/f/d) for the Central Manufacturing Engineering department (cross‑program and new development).
Freizeitausgleich Nach Möglichkeit Arbeiten aus dem Homeoffice Individuelle Betreuung durch Ihre/n persönliche/n CENIS AnsprechpartnerIn „MitarbeiterInnen-werben-MitarbeiterInnen-Prämie“ in Höhe von bis zu 1.500 Euro Starten Sie mit uns durch und übernehmen Sie gerne Verantwortung in der unten beschriebenen Position. / Take the next step in your career and take on responsibility in the position described below. In this role, you will oversee and optimize end-to-end supply chain processes while ensuring the highest quality standards within Airbus operations.
Dann bieten wir Ihnen eine spannende Möglichkeit: Im Auftrag unseres Kunden einem der führenden Energieübertragungsunternehmen Europas suchen wir einen erfahrenen Project Quality Manager (m/w/d) an den Standorten Bayreuth, Lehrte und Bremen. In dieser verantwortungsvollen Position sorgen Sie dafür, dass Qualitätsstandards in großen Energieinfrastrukturprojekten konsequent eingehalten, weiterentwickelt und gelebt werden.
#Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #Compensation: Commitment deserves reward – overtime or multi-day assignments are additionally compensated.
Ab 01.04.2027 wechselt unser Kunden seinen Standort nach 63505 Langenselbold, welcher im Main-Kinzig-Kreis liegt. In dieser Position stellen Sie die Einhaltung regulatorischer Anforderungen (cGMP/GxP) sicher, indem Sie Prozesse, Systeme und Änderungen im pharmazeutischen Distributionsumfeld compliant gestalten, überwachen und kontinuierlich verbessern.
Ensuring regular talks and meetings with the relevant Customers’ contact persons to contribute to smooth relationships and anticipate any of their needs.Trigging, leading and implementing actions intending to raise the standards delivered to Customers.Ensuring training of local Q&FS Teams to understand Customers’ expectations and optimal way to handle their requestsEnsuring a high level of harmonization in the way plants handle all Q&FS-related matters with CustomersManaging the KPIs measuring the Q&FS performances with CustomersSupporting all plants supplying Customers so that they all get the highest audit and overall assessment scoring from Key Accounts The position will be based in Paris Area and requires mobility for visiting plants or customers’ headquarters (around 20% of time). DAS BRINGEN SIE MIT MSC in Food or Chemical process degree with a significant background in Quality Management 6 years of experience minimum, in Quality Assurance or Food Safety in Food or Cosmetics Ingredients Business Proven international project management experience in a matrix worldwide organizationFluent in French and EnglishCustomer oriented Good relationship building both internally and externally : excellent communication and interpersonal skills, listening capabilities, helpful oriented, capable of adapting quickly and efficientlyBusiness minded and negociations skillsAbility to work cross-functionally and to meet deadlines, well-organizedRigorous, Autonomous, persevering, capacity to propose new ideas DAS ANGEBOT FÜR SIE If you are interested in this position, please contact :
DAS BRINGEN SIE MIT BSc or MSc degree in Technology, Chemistry or MicrobiologyRelevant work experience in Quality Management in the food industry, preferably in a comparable business environmentDetailed knowledge of food safety standards, QA systems and actual quality topicsStrong managerial skills, both people management as well as project management with cross functional teamsComfortable working in an international and dynamic matrix organisation with various external and internal stakeholders Personal skills: independent, overview, convincing, well organised, decisive, results driven and persistence. DAS ANGEBOT FÜR SIE If you are interested in this position, please contact Hans Hilbrands, telephone: +31 (0)317-468686 / +31 (0)6-51025152 or apply through our website or e-mail your written application to DSM Food Specialities selected DUPP for this vacancy as the only partner in the recruitment process.
Lead and continuously improve the GMP self-inspection program, including annual planning and executionCoach SMEs and audit teams to ensure strong inspection and self-inspection readinessPerform gap assessments on global procedures and drive alignment across site functionsCoordinate cross-functional activities and ensure effective communication with all departmentsSupport internal, external, and mock audit preparation, including document review and QA inputAct as backroom/ACC or scribe team member during audits and inspectionsServe as Data Integrity Champion and ensure consistent DI implementation across the sitePrepare and present compliance topics to the Quality Council and site leadershipSupport continuous improvement initiatives and coordinate operational activities within the compliance teamAct as back-up for the Quality Compliance & Systems Expert when required University degree in biochemistry, chemistry, engineering, or another relevant scientific/technical disciplineSolid experience in biotechnology and/or pharmaceutical industryStrong knowledge of GMP requirements and Quality SystemsUnderstanding of manufacturing, QC laboratory, and warehouse processes for biological productsSolid knowledge of Good Documentation Practices (GDDP) and Data Integrity principlesExperience supporting audits and regulatory inspectionsSkilled in writing, reviewing, and updating SOPs and technical documentationFamiliarity with risk management tools (FMEA, RCA, etc.)Proficiency in French and English (minimum B2)Experience with eQMS tools (e.g., Veeva Vault, TrackWise), Microsoft Office, SharePoint, and Power BI A very renowned companyContinuous support during the assignmentIndividual all-round care: Support throughout the entire application phase Ihr Kontakt Referenznummer 864224/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Zusätzlich genießt du zahlreiche Social Benefits (Mitarbeiter*innen-Restaurant / Unterstützung für Mittagessen, Inhouse-Pub / Lounge, Gratis-Parkplätze, umfangreiches Sportangebot, zahlreiche Mitarbeiter*innen-Events, Sprachkurse, …) Das Mindestgehalt für diese Position liegt – abhängig von Qualifikation und Erfahrung – bei € 80.000, -- brutto pro Jahr. Das Jahresgehalt setzt sich zusammen aus 14 Monatsgehältern und einer garantierten Prämie.
Proficiency in French and English (minimum B2) Experience with eQMS tools (e.g., Veeva Vault, TrackWise), Microsoft Office, SharePoint, and Power BI A very renowned company Continuous support during the assignment Individual all-round care: Support throughout the entire application phase Ihr Kontakt Referenznummer 864224/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Betriebliche Altersvorsorge, Zuschuss zu vermögenswirksamen Leistungen. Viele weitere Benefits Wenn Sie Interesse an dieser Position haben, freue ich mich auf Ihre Bewerbung und darauf, Sie persönlich bei Ihrer nächsten Karrierestation zu unterstützen. Ihre Unterlagen können Sie direkt an mich senden . ich begleite Sie professionell durch den gesamten Auswahlprozess.
Betriebliche Altersvorsorge, Zuschuss zu vermögenswirksamen Leistungen. Viele weitere Benefits Wenn Sie Interesse an dieser Position haben, freue ich mich auf Ihre Bewerbung und darauf, Sie persönlich bei Ihrer nächsten Karrierestation zu unterstützen. Ihre Unterlagen können Sie direkt an mich senden . ich begleite Sie professionell durch den gesamten Auswahlprozess.
Follow up on the KPIs related to their area of responsibility and take the necessary actions to comply with them.Ensure compliance with the requirements related to the position indicated in the IATF 16949, ISO 14001 and ISO 45001 standards, specific customer requirements and the legal requirements of the area.Actively participate in the processes of Continuous Improvement and root cause analysisDaily monitoring of the client's portals, or any other logistical notification received by them electronically or by other means, ensures that the required information is uploaded into the customer portals and on the Q-module on SAP.
We are currently looking for a skilled & passionate Senior Quality Assurance Manager (m/w/d) to become part of our App & Web Team at ABOUT YOU onsite in Hamburg or Berlin. This position is focused on testing the discovery & consideration experience in the ABOUT YOU mobile app. Our App & Web Team constantly improves the App, Mobile Website and Desktop Website.
Aktuell suchen wir Sie am Standort Biberach an der Riß für folgende attraktive Position, Document Specialist Quality (m/w/d) in Teilzeit 50 % Es handelt sich bei dieser Position um ein hybrides Arbeitsmodell, welches an 4 Tagen pro Woche nach Absprache bzw. nach Bedarf aus dem Home Office/remote abgedeckt werden kann.
Aktuell suchen wir Sie am Standort in Ochsenhausen für folgende attraktive Position: QC Expert (m/w/d) Quality Control / Pharma Development / GMP Nutzen Sie Ihre Chance und werden Sie Teil dieser Erfolgsgeschichte!
Registrieren Sie sich und freuen Sie sich auf interessante und passende Positionen und Projekte. Erstellung und Pflege des PQMP: Entwickeln, dokumentieren, implementieren und kontinuierlich verbessern des Project Quality Management Plans (PQMP) gemäß den Vertragsanforderungen und internen ProzessenKritikalitätsbewertung: Mit strukturierten Techniken (z.B.
Registrieren Sie sich und freuen Sie sich auf interessante und passende Positionen und Projekte. Erstellung und Pflege des PQMP: Entwickeln, dokumentieren, implementieren und kontinuierlich verbessern des Project Quality Management Plans (PQMP) gemäß den Vertragsanforderungen und internen Prozessen Kritikalitätsbewertung: Mit strukturierten Techniken (z.B.
Ein gern gesehener Mehrwert sind Erfahrungen mit dem V-ModellErste, sehr gerne auch fundierte Erfahrung im Qualitätsmanagement, bevorzugt nach ISO 13485 für das Design und die Herstellung von Medizinprodukten sind bei Ihnen gegeben Kenntnisse in Cybersecurity, Risikomanagements Medizinprodukte (ISO 14971) und Usability Engineerings (IEC 62366-1/-2) sind von Vorteil aber kein Muss Gute Deutsch- und Englischkenntnisse in Wort und Schrift runden Ihr Profil ab Die Chance Eine sehr interessante und verantwortungsvolle Aufgabe in der High End Mess- und MedizintechnikVielfältige Entwicklungsmöglichkeiten: Eine spannende Position mit zahlreichen Weiterentwicklungschancen in der MedizintechnikSicherer Arbeitsplatz: Ein sicherer Job in einem etablierten, erfolgreichen, expandierenden internationalen Unternehmen mit einem sehr gutem ArbeitsklimaFlexibilität: Flexible Arbeitszeiten und Regelungen zum mobilen ArbeitenAttraktives Gehalt: Ein umfangreiches und attraktives Gehaltspaket mit einer betrieblichen AltersvorsorgeZusatzleistungen: Hansefit, Jobticket, JobRad und weitere freiwillige Leistungen wie Kinderbetreuung bzw.
Die Experten für nationales und internationales Headhunting entwickeln im Kundenauftrag individuelle Suchstrategien, um Positionen mit Kandidaten zu besetzen, die perfekt zur Unternehmenskultur passen. Das Unternehmen erhielt zahlreiche Auszeichnungen für seine Personalberatung.
Sie profitieren von persönlicher Beratung, klarer Kommunikation, diskreter Vermittlung und realistischen Karrierechancen ohne unpassende Jobvorschläge oder Massenabfertigung. Unser Anspruch ist es, Positionen zu finden, die fachlich, menschlich und langfristig zu Ihnen passen. Werden Sie Teil der Frielingsdorf GmbH und nutzen Sie die Vorteile eines spezialisierten Personalberaters, der Ihre Branche kennt und Ihre berufliche Entwicklung aktiv begleitet.
Freizeitausgleich Nach Möglichkeit Arbeiten aus dem Homeoffice Individuelle Betreuung durch Ihre/n persönliche/n CENIS AnsprechpartnerIn „MitarbeiterInnen-werben-MitarbeiterInnen-Prämie“ in Höhe von bis zu 1.500 Euro Starten Sie mit uns durch und übernehmen Sie gerne Verantwortung in der unten beschriebenen Position. Starten Sie als Project and Problem‑Solving Manager (m/w/d) im Bereich Qualitätssicherung (programmsübergreifend) und übernehmen Sie folgende Aufgaben: Führung und Steuerung komplexer Qualitätsthemen sowie kontinuierlicher Verbesserungsprojekte Definition und Weiterentwicklung von Maßnahmenstandards Identifikation von Verbesserungspotenzialen und Unterstützung bei deren Umsetzung Unterstützung von Produktions‑ und Qualitätsprozessen Durchführung von Operational Surveillance Ziel ist die Verbesserung: der Prozessleistung und der Einhaltung von Produktstandards der Prozesszuverlässigkeit der Prozesswiederholbarkeit – sowohl in der initialen Designphase, vor Prozessänderungen als auch kontinuierlich während des gesamten Produktlebenszyklus Das bringen Sie mit: Abgeschlossene Weiterbildung zum Fachwirt (m/w/d) oder Techniker (m/w/d) im technischen Bereich, oder ein Abschluss in Projektmanagement, Luft‑ und Raumfahrt, Betriebswirtschaftslehre oder eine vergleichbare Qualifikation Berufserfahrung im Projektmanagement, in der Prozessverbesserung sowie im Qualitätsmanagement Gute Kenntnisse in KVP, Lean Management und Total Quality Management (Problemlösungsmethoden) Gute Kenntnisse im Umgang mit Google Workspace Verhandlungssichere Deutsch‑ und Englischkenntnisse Fähigkeit, Zusammenhänge und Funktionsweisen schnell zu erkennen und zu analysieren Selbstständige, strukturierte und ergebnisorientierte Arbeitsweise zur termingerechten Zielerreichung und effizienten Koordination von Arbeitsabläufen Ausgeprägte kommunikative Fähigkeiten zur erfolgreichen Zusammenarbeit mit Ansprechpartnern auf allen Hierarchieebenen Wir freuen uns auf Ihre aussagekräftige Bewerbung.
Initiate and formulate proposals / business cases for quality improvement projects including deliverables and planning for the development and implementation of proposed improvements Create and maintain supplier records in the qualification system Assess material changes and drive required quality change controlsSupport supplier qualification activities and coordinate supplier auditsManage supplier relationships to ensure value delivery and site performanceDevelop material specifications to support qualification and releaseCoordinate material release schedules to secure on-time production supplyCollaborate with tech transfer, procurement, quality, and manufacturing on supplier and material selectionEnsure materials meet required quality grades for clinical manufacturingAlign purchase orders and material planning with lead times, safety, quality, cost, and production schedulesSupport quality investigations, risk assessments, and continuous improvement initiatives including business case development.Bachelor’s or Master’s degree in engineering, pharmacy or science related field or profound experience working in a relevant academic or industry field Renowned pharmaceutical companyLong term contractAttractive salary package25 Days Holiday Ihr Kontakt Referenznummer 863542/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Initiate and formulate proposals / business cases for quality improvement projects including deliverables and planning for the development and implementation of proposed improvements Create and maintain supplier records in the qualification system Assess material changes and drive required quality change controls Support supplier qualification activities and coordinate supplier audits Manage supplier relationships to ensure value delivery and site performance Develop material specifications to support qualification and release Coordinate material release schedules to secure on-time production supply Collaborate with tech transfer, procurement, quality, and manufacturing on supplier and material selection Ensure materials meet required quality grades for clinical manufacturing Align purchase orders and material planning with lead times, safety, quality, cost, and production schedules Support quality investigations, risk assessments, and continuous improvement initiatives including business case development.Bachelor’s or Master’s degree in engineering, pharmacy or science related field or profound experience working in a relevant academic or industry field Renowned pharmaceutical company Long term contract Attractive salary package 25 Days Holiday Ihr Kontakt Referenznummer 863542/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
At the earliest possible date we are looking forAssembly Electrical Degree in Electrical Engineering related and finished with a Bachelor Degree Minimum of 3 years’ experience in similar position Capable of executing solder activity Capable of using VOM meter Assembler-Mechanics Must be able to read pneumatic and electrical schematics.
At the earliest possible date we are looking forAssembly Electrical Degree in Electrical Engineering related and finished with a Bachelor Degree Minimum of 3 years’ experience in similar position Capable of executing solder activityCapable of using VOM meter Assembler-Mechanics Must be able to read pneumatic and electrical schematics.
At the earliest possible date we are looking forAssembly Electrical Degree in Electrical Engineering related and finished with a Bachelor Degree Minimum of 3 years’ experience in similar position Capable of executing solder activityCapable of using VOM meter Assembler-Mechanics Must be able to read pneumatic and electrical schematics.
Erfahrung Du verfügst über umfangreiche Führungserfahrung – entweder direkt im Qualitätsmanagement oder in einer technischen Position, in der du eng mit dem QM-Bereich zusammengearbeitet hast. Zudem besitzt du fundierte Kenntnisse in Qualitätsprozessen innerhalb der Bereiche Forschung & Entwicklung, Engineering sowie Kundenprojekte einschließlich EPC-Umfeld.
The Study Physician is a critical global role responsible for assuming medical oversight of clinical trials within Clinical Development & Operations. This position requires a qualified and clinically experienced physician who will provide comprehensive medical expertise throughout all phases of the trial—from preparation and conduct to reporting.
Register now and look forward to many interesting and suitable positions and projects. Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company at the intersection of advanced materials science and modern rocket propulsion.
You will report to the Quality Control Manager and operate as a senior specialist working closely with production, while maintaining functional independence from Production and Process Engineering. This is not a team-lead position, but a hands-on expert role with significant technical authority. Working hours & shift setup: The role starts on day shift. As production scales, FPRT will transition to 24/7 operations, and the role is expected to move into a three-shift rotation.
#Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #Compensation: Commitment deserves reward – overtime or multi-day assignments are additionally compensated.
#Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #Compensation: Commitment deserves reward – overtime or multi-day assignments are additionally compensated.
#Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #Compensation: Commitment deserves reward – overtime or multi-day assignments are additionally compensated.
#Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #Compensation: Commitment deserves reward – overtime or multi-day assignments are additionally compensated.
Performs testing of samples linked to operations, validation, utilities and environmental monitoring samplesCoordinate and work on the transfer, development and validation of analytical methods including qualification of equipment needed for analysisCoordination in maintenance, calibration and use of laboratory equipmentActively contribute to the GMP Inspection Readiness of QC to ensure the fully compliance of relevant Quality System and Procedural documentsActively contribute to the QC operational readiness managing projects (external and internal) and the assigned to ressources (including coordination of people daily tasks)Participates in the transfer, development and validation of analytical methods including qualification of equipment needed for analysisCreation and revision of guidance documents such as SOPs/ WIs and other related documents Master’s degree or higher in Life Sciences, Chemistry, Biochemistry, or a related scientific field (lower educational background acceptable with relevant experience)Solid experience in chemical or biochemical laboratories, including work in a regulated GMP environmentExperience performing analytical testing of samples related to operations, validation, utilities, and environmental monitoringStrong expertise in analytical method transfer, development, and validationExperience with qualification, maintenance, and calibration of analytical laboratory equipmentSolid understanding of GMP regulations, quality systems, and inspection readiness within QC laboratoriesExperience in creating and revising SOPs, work instructions, and other quality documentationAbility to coordinate QC activities and support operational readiness projects in laboratory environmentsStrong collaboration and communication skills, working effectively across cross functional teamsDemonstrated ability to drive results, adapt quickly to changing situations, and maintain a strong business and quality focus Renowned pharmaceutical company Attractive salary package HAYS Benefits Ihr Kontakt Referenznummer 864632/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Own, author, record and investigate Deviations across operations Collaborate with Subject Matter Experts and key stakeholders to determine root causes and assess product or system impact Apply structured investigational tools such as Fault Tree Analysis, Event & Causal Factors Chart, Fishbone Diagram and similar methodologies Define effective CAPAs and associated effectiveness checks to prevent recurrence Ensure full cGMP compliance throughout the investigation lifecycle Drive quality records to timely and accurate completion Support continuous improvement activities within operations Contribute to enhancing investigation quality, consistency and efficiency Maintain strong documentation standards and technical writing quality Communicate investigation progress and outcomes to relevant stakeholders Bachelor’s degree in chemistry, biotechnology, life sciences or a related field Experience with Deviations and cGMP in a regulated pharmaceutical or API environment is a strong advantage Knowledge of biotech manufacturing processes and analytical methods is an advantage Experience with Human and Organizational Performance and risk management approaches is beneficial Fluency in English in both written and spoken form; German is an advantage Strong technical writing, analytical and communication skills Structured, focused and well-organised working style Open-minded, agile, highly motivated and adaptable to change Strong interpersonal and collaboration skills with a proactive mindset Ability to manage multiple investigations simultaneously in a dynamic environment Opportunity to work in a state-of-the-art large-scale mammalian manufacturing environment Exposure to cross-functional teams and complex deviation management processes Impactful role with high visibility in quality and operations functions Inclusive, international and collaborative workplace culture Ihr Kontakt Referenznummer 863146/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Performs testing of samples linked to operations, validation, utilities and environmental monitoring samples Coordinate and work on the transfer, development and validation of analytical methods including qualification of equipment needed for analysis Coordination in maintenance, calibration and use of laboratory equipment Actively contribute to the GMP Inspection Readiness of QC to ensure the fully compliance of relevant Quality System and Procedural documents Actively contribute to the QC operational readiness managing projects (external and internal) and the assigned to ressources (including coordination of people daily tasks) Participates in the transfer, development and validation of analytical methods including qualification of equipment needed for analysis Creation and revision of guidance documents such as SOPs/ WIs and other related documents Master’s degree or higher in Life Sciences, Chemistry, Biochemistry, or a related scientific field (lower educational background acceptable with relevant experience) Solid experience in chemical or biochemical laboratories, including work in a regulated GMP environment Experience performing analytical testing of samples related to operations, validation, utilities, and environmental monitoring Strong expertise in analytical method transfer, development, and validation Experience with qualification, maintenance, and calibration of analytical laboratory equipment Solid understanding of GMP regulations, quality systems, and inspection readiness within QC laboratories Experience in creating and revising SOPs, work instructions, and other quality documentation Ability to coordinate QC activities and support operational readiness projects in laboratory environments Strong collaboration and communication skills, working effectively across cross functional teams Demonstrated ability to drive results, adapt quickly to changing situations, and maintain a strong business and quality focus Renowned pharmaceutical company Attractive salary package HAYS Benefits Ihr Kontakt Referenznummer 864632/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
As well as providing a significant contribution to the clinical workload, the successful candidate will have opportunities to be involved in training junior embryologists, internal quality control, donor recruitment, organising imports/exports and supporting in the management of stored gametes/embryos. This is a full time position working 37.5 hour per week There will be on-call and weekend working required on a rotational basis The Location: Oxford Fertility was established in 1992 and is one of the UK’s longest standing and largest IVF clinics.
Registrieren Sie sich und freuen Sie sich auf interessante und passende Positionen und Projekte. Mein Arbeitgeber Als modernes Unternehmen entwickelt sich unser Mandant ständig weiter und geht dabei immer wieder neue Wege.
Denn durch unsere intensiven Beziehungen und Netzwerke über alle Industriebranchen hinweg vermitteln wir Ihnen als Engineering-Fachleuten spannende Projekte und attraktive Positionen. Ganz nach Ihren Interessen und abhängig von Ihren Erfahrungen und Qualifikationen. Sie profitieren dabei von einer professionellen Betreuung von der ersten Ansprache bis zum Antritt Ihres neuen Projektes bzw.
Denn durch unsere intensiven Beziehungen und Netzwerke über alle Industriebranchen hinweg vermitteln wir Ihnen als Engineering-Fachleuten spannende Projekte und attraktive Positionen. Ganz nach Ihren Interessen und abhängig von Ihren Erfahrungen und Qualifikationen. Sie profitieren dabei von einer professionellen Betreuung von der ersten Ansprache bis zum Antritt Ihres neuen Projektes bzw.
Registrieren Sie sich und freuen Sie sich auf interessante und passende Positionen und Projekte. Mein Arbeitgeber Als modernes Unternehmen entwickelt sich unser Mandant ständig weiter und geht dabei immer wieder neue Wege.
#Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #Compensation: Commitment deserves reward – overtime or multi-day assignments are additionally compensated.
#Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #Compensation: Commitment deserves reward – overtime or multi-day assignments are additionally compensated.
Own, author, record and investigate Deviations across operationsCollaborate with Subject Matter Experts and key stakeholders to determine root causes and assess product or system impactApply structured investigational tools such as Fault Tree Analysis, Event & Causal Factors Chart, Fishbone Diagram and similar methodologiesDefine effective CAPAs and associated effectiveness checks to prevent recurrenceEnsure full cGMP compliance throughout the investigation lifecycleDrive quality records to timely and accurate completionSupport continuous improvement activities within operationsContribute to enhancing investigation quality, consistency and efficiencyMaintain strong documentation standards and technical writing qualityCommunicate investigation progress and outcomes to relevant stakeholders Bachelor’s degree in chemistry, biotechnology, life sciences or a related fieldExperience with Deviations and cGMP in a regulated pharmaceutical or API environment is a strong advantageKnowledge of biotech manufacturing processes and analytical methods is an advantageExperience with Human and Organizational Performance and risk management approaches is beneficialFluency in English in both written and spoken form; German is an advantageStrong technical writing, analytical and communication skillsStructured, focused and well-organised working styleOpen-minded, agile, highly motivated and adaptable to changeStrong interpersonal and collaboration skills with a proactive mindsetAbility to manage multiple investigations simultaneously in a dynamic environment Opportunity to work in a state-of-the-art large-scale mammalian manufacturing environmentExposure to cross-functional teams and complex deviation management processesImpactful role with high visibility in quality and operations functionsInclusive, international and collaborative workplace culture Ihr Kontakt Referenznummer 863146/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register now and look forward to many interesting and suitable positions and projects. Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company at the intersection of advanced chemistry and modern rocket propulsion.
Register now and look forward to many interesting and suitable positions and projects. Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company at the intersection of advanced chemistry and modern rocket propulsion.