Stellen in basel

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

Für über 500 verschiedene Berufe suchen wir motivierte Mitarbeiter. Und das in ganz Deutschland. Ob erfahrene Profis oder Berufsstarter - wir bieten zahlreiche Einstiegs- und Weiterbildungsmöglichkeiten. Zum 01. Februar 2020 suchen wir Dich für den Quereinstieg zum Lokführer (w/m/d) für das Geschäftsfeld DB Fernverkehr an dem Standort Basel Badischer Bahnhof. Deine Aufgaben: ..... klicken sie bewerben, für die volle Stellenbeschreibung

Die weltweiten Herausforderungen der Energiewende von der Energieerzeugung bis hin zur Energieverteilung erfordern innovative Lösungen in der Hochspannungsprüf- und -messtechnik. ln diesem Marktsegment gehört die HAEFELY-HIPOTRONICS mit Sitz in Basel und Brewster/USA mit ihrer mehr als 100jährigen Firmengeschichte zu den weltweit führenden Anbietern. ..... klicken sie bewerben, für die volle Stellenbeschreibung

Die weltweiten Herausforderungen in der Energieerzeugung und in der Energieverteilung erfordern innovative Lösungen in der Hochspannungsprüf- und -messtechnik. ln diesem Marktsegment gehört die HAEFELY HIPOTRONICS mit Sitz in Basel und Brewster/USA mit ihrer mehr als 100jährigen Firmengeschichte zu den weltweit führenden Anbietern. Auftragsbezogene Planung von..... klicken sie bewerben, für die volle Stellenbeschreibung

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

Die Celonic Group ist ein international tätiges Dienstleistungsunternehmen (CDMO - Contract Development Manufacturing Organization) für die biopharmazeutische Industrie mit Standorten in Basel und Heidelberg. Als CDMO bieten wir Services zur Produktion von Biopharmazeutika an, beginnend bei der Zelllinienentwicklung bis zur GMP-gerechten Herstellung von therapeutischen Proteinen für..... klicken sie bewerben, für die volle Stellenbeschreibung

At Roche, we believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are brave in both decision and action, we believe that good business means a better world. As a key finance function under Global Product Development PDMA (Product Development Medical Affairs) Finance business..... click apply for full job details

(Senior) Research Associate - Innovative Cell Models to study the fate of therapeutic proteins Basel At Roche, we believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives and we are fearless in both decision and action. And we believe that good business means a better world. That is why we come to work every single day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. Roche Pharma Research and Early Development (pRED) translates extraordinary science into medical innovation through a diversity of technologies and talent located across seven research sites worldwide. We deliver on individual patient needs through a deep understanding of disease biology and the implementation of Personalized Healthcare strategies. You would like to play an active part in the way how we assess our innovative therapeutic protein drugs in the future? We are searching for a highly motivated Research Associate to join the Cellular Transport group. The team is part of Investigative Safety within Pharmaceutical Sciences at the Roche Innovation Center Basel. The department is a well-established and respected group of 80 people responsible for the conduct of all in vitro work to determine the disposition and safety of new Roche medicines. Our group focuses on the use of cutting-edge cell biology methods to investigate the transport and disposition of new chemical entities (including biologics), with a strong focus on the blood-brain barrier. In this position you will: Develop and apply human 3D models of the blood-brain barrier to characterize transport properties of biologics Use advanced microscopy techniques and FACS to visualize and quantify membrane receptor dynamics and intracellular transport processes Be responsible for maintaining a molecular cell biology lab; planning, conducting and documenting in vitro studies Report and present results of studies within internal group meetings Interact with a multidisciplinary group to help advance projects across the portfolio We are looking for: Bachelor/MSc degree in biological sciences with relevant industry experience (1-5 years) Strong expertise in cell culture and handling of multiple cell types. Experience in using advanced cellular models (iPSc, spheroids, organ-on-chip) is highly desirable. Experience using confocal microscopy to design imaging-based assays. High degree of self-motivation and ability to independently conduct experiments Strong communication, interpersonal, and organizational skills Interest in working in a multidisciplinary and multinational environment Good knowledge of written and oral English

Production Engineer - Monitors - Medical A fast-growing medical devices company located in Basel are looking for a Production Engineer to join them on a permanent basis at their offices in Basel. This is a great opportunity to be part of the growth and direction of an innovative med tech company. Responsibilities Construction & commissioning of a new production of medical monitors Design, procurement and maintenance of production and test facilities Planning and execution of plant production plans Create and maintain the production-related documentation Training of production staff Requirements: Studies/FH/Degree in electrical engineering/production/engineering Experience in the assembly of electromechanical devices Experience in project management and industrialization of new products Good German and English skills For more information, please click apply and someone will be in touch to discuss in more detail

Electronics Technician / Medical Devices / Basel A fast-growing medical devices company located in Basel are looking for a Electronics Technician to join them on a permanent basis at their offices in Basel. This is a great opportunity to be part of the growth and direction of an innovative med tech company. Responsibilities: Electronics development, including prototype construction and testing CAD/CAE for schematics layout (in Altium) Participation in the production transfer, incl. specification and construction of test equipment and test setups Support production / QA / Fault Analysis Requirements Completed apprenticeship as an electronics engineer / FH or similar Professional experience from industrial environment High interest in technology and electronics Languages: German (spoken & written) and basic English For more information, please click apply and someone will be in touch to discuss in more detail

Electronics Group Leader - Medical Devices - Basel A fast-growing medical devices company located in Basel are looking for a Electronics Group Leader to join them on a permanent basis at their offices in Basel. This is a great opportunity to be part of the growth and direction of an innovative med tech company. Job role: Leadership of the electronics group (4 people) Lead, advise, input and oversee design & development projects Definition and specification of new products Design responsibility electronic assemblies and interfaces Overall responsibility for development and manufacturability of existing electronics assemblies (devices and sensors) Requirements: Degree in electrical engineering/electronics/engineering, solid electronics expertise At least 5 years' experience working in the medical devices sector Knowledge of electrical safety, EMC, etc. Languages ??German and English in writing and in writing (C1) For more information, please click apply and someone will be in touch to discuss in more detail.

Junior Product Manager - Medical Devices - Basel An innovative company that design, develop and produce medical devices are looking for a Junior Product Manager to join them on a permanent basis at their offices in Basel. Key tasks: Analysis of market segments and development of new product positionings based on market insights Lead interdisciplinary project teams and support product launches Coordinate clinical application studies and run product training Develop sales and marketing toolkits (videos, brochures, application notes, webpage, etc.) Experience required: Clinical background as intensive care nurse or respiratory therapist Eager to learn and develop in a dynamic environment Fluent in English, conversational German For more information, please click apply and someone will be in touch to discuss in more detail

QM/RA Manager - Medical Devices - Basel A company that design, develop and produce medical devices are looking for a QM/RA Manager to join their team on a permanent basis. In this role you will have responsibility for the QM / RA and be a member of the management team. Key tasks: Play an integral part of the management team, looking after all topics relating to QM/RA Responsible for maintaining, updating and Improvement of the QM Systems (EN ISO 13485, MDR) Responsible for the approval our products and implementation of internal and external audits Experience required: Excellent experience in QM/RA in a highly regulated industry Very good English & German, written and spoken For more information, please click apply and some one will be in touch to discus the role in more detail

Jungbunzlauer ist einer der weltweit führenden Hersteller von Inhaltsstoffen auf natürlicher Basis. Die Gruppe betreibt Produktionswerke in Österreich, Kanada, Deutschland und Frankreich und ist spezialisiert auf hochwertige Ingredienzien für die Lebensmittel-, Getränke-, Pharma- und Kosmetikindustrie sowie für verschiedene technische Anwendungen. Als einer der "Hidden Champions des 21..... klicken sie bewerben, für die volle Stellenbeschreibung

Wir arbeiten für eine führende und stark wachsende Unternehmensgruppe mit Hauptsitz bei Basel in der Schweiz. Das Unternehmen beschäftigt heute ca. 1.400 Mitarbeiter an acht verschiedenen Standorten in Europa und den USA. Die Gruppe ist ein CDMO und entwickelt und produziert im Auftrag ihrer Kunden als „Full-Service"-Dienstleister pharmazeutische Wirkstoffe - APIs -..... klicken sie bewerben, für die volle Stellenbeschreibung

Die weltweiten Herausforderungen in der Energieerzeugung und in der Energieverteilung erfordern innovative Lösungen in der Hochspannungsprüf- und -messtechnik. ln diesem Marktsegment gehört die HAEFELY HIPOTRONICS mit Sitz in Basel und Brewster/USA mit ihrer mehr als 100jährigen Firmengeschichte zu den weltweit führenden Anbietern. Abarbeitung von übertragenen Arbeitspaketen/..... klicken sie bewerben, für die volle Stellenbeschreibung

Senior QA Manager Drug Substance (GMP/GDP) - Basel, Switzerland Jocelyn Blackham is recruiting for a Senior QA Manager Drug Substance (GMP/GDP) to join a rapidly growing company in the drug discovery area. The position will be offered on a 6-12 month contract at our clients site in Basel, with the possibility of extension. The main purpose of the role will be to: - Provide GMP/GDP quality assurance expertise during development and later during commercialization of products. - Perform GMP onsite audits at Contract Manufacturing Organizations (CMOs). - Prepare GMP/GDP Agreements in collaboration with CMOs and the CMC team. - Write, review, and/or approve internal SOPs and other GMP/GDP related documentation. - Ensure that medicinal products are designed, developed, manufactured and controlled according to quality standards. - Establish a quality risk management approach in projects based on ICH Q9 concepts to ensure that quality is understood and managed by all stakeholders throughout the product life cycle. - Manage all required activities to support release of active ingredients, investigational medicinal products including approval of master process documentation, batch record review, resolution of investigations, and assessment of change controls. Further responsibilities will include: - Notifying management of potential quality and regulatory issues. - Providing guidance on the resolution of complaints, testing issues, discrepancies and Out of Specifications, investigations and Corrective and Preventive Actions as needed, on assigned projects. - Supporting the review and optimization of the company's pharmaceutical quality system by establishing and preparing review of relevant Key Performance Indicators. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Advanced University degree in Pharmacy, Chemistry or alternative technical/science university degree. - Previous experience in different positions like pharmaceutical or chemical development, quality control, analytical development, chemical or pharmaceutical production or similar operational positions in the pharmaceutical industry. - Previous experience in quality assurance activities specific to drug substance. - Excellent knowledge of GMPs and regulatory environments, ability to interpret and implement quality standards. - Strong interpersonal and influencing skills. - Entrepreneurial mind set combined with cost consciousness. This is an excellent opportunity to join a expanding pharmaceutical company. Please quote reference 45874 in all correspondence.

Alex Tosney is recruiting for a HPLC Analyst to join a company in the rapidly growing drug discovery area at their site based in Basel on a contract basis for 6 months. The main purpose of the role will be: - Analytical method validation. - Supporting the creation and review of validation protocols. - Analytical method development. - Drafting specifications and stability protocols for drug substance testing. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - GMP experience in the pharmaceutical industry. - HPLC experience, Empower would be ideal. - Method development and validation experience. - Knowledge in HRMS, NMR and GC would be beneficial. This is an excellent opportunity to join a rapidly growing biopharmaceutical company. Please could you send any correspondence in English. Please quote reference 46007 in all correspondence.

Production Engineer - Monitors - Medical A fast-growing medical devices company located in Basel are looking for a Production Engineer to join them on a permanent basis at their offices in Basel. This is a great opportunity to be part of the growth and direction of an innovative med tech company. Responsibilities Construction & commissioning of a new production of medical monitors Design, procurement and maintenance of production and test facilities Planning and execution of plant production plans Create and maintain the production-related documentation Training of production staff Requirements: Studies/FH/Degree in electrical engineering/production/engineering Experience in the assembly of electromechanical devices Experience in project management and industrialization of new products Good German and English skills For more information, please click apply and someone will be in touch to discuss in more detail

Electronics Technician / Medical Devices / Basel A fast-growing medical devices company located in Basel are looking for a Electronics Technician to join them on a permanent basis at their offices in Basel. This is a great opportunity to be part of the growth and direction of an innovative med tech company. Responsibilities: Electronics development, including prototype construction and testing CAD/CAE for schematics layout (in Altium) Participation in the production transfer, incl. specification and construction of test equipment and test setups Support production / QA / Fault Analysis Requirements Completed apprenticeship as an electronics engineer / FH or similar Professional experience from industrial environment High interest in technology and electronics Languages: German (spoken & written) and basic English For more information, please click apply and someone will be in touch to discuss in more detail

Electronics Group Leader - Medical Devices - Basel A fast-growing medical devices company located in Basel are looking for a Electronics Group Leader to join them on a permanent basis at their offices in Basel. This is a great opportunity to be part of the growth and direction of an innovative med tech company. Job role: Leadership of the electronics group (4 people) Lead, advise, input and oversee design & development projects Definition and specification of new products Design responsibility electronic assemblies and interfaces Overall responsibility for development and manufacturability of existing electronics assemblies (devices and sensors) Requirements: Degree in electrical engineering/electronics/engineering, solid electronics expertise At least 5 years' experience working in the medical devices sector Knowledge of electrical safety, EMC, etc. Languages ??German and English in writing and in writing (C1) For more information, please click apply and someone will be in touch to discuss in more detail.

Alex Tosney is recruiting for a HPLC Analyst to join a company in the rapidly growing drug discovery area at their site based in Basel on a contract basis for 6 months. The main purpose of the role will be: - Analytical method validation. - Supporting the creation and review of validation protocols. - Analytical method development. - Drafting specifications and stability protocols for drug substance testing. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - GMP experience in the pharmaceutical industry. - HPLC experience, Empower would be ideal. - Method development and validation experience. - Knowledge in HRMS, NMR and GC would be beneficial. This is an excellent opportunity to join a rapidly growing biopharmaceutical company. Please could you send any correspondence in English. Please quote reference 46007 in all correspondence.

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

Als unabhängiges Familienunternehmen entwickeln und gestalten wir zukünftige Lebensräume. Mit gemeinsamem Wissen und Ihrer Leidenschaft schaffen wir im Team wegweisende Lösungen. Wir sind eine führende Schweizer Planungs- und Beratungsgruppe mit rund 450 Mitarbeiterinnen und Mitarbeitern. Innerhalb der Rapp Gruppe entwickeln die Berater/-innen der Rapp Trans AG optimale Lösungen für den..... klicken sie bewerben, für die volle Stellenbeschreibung

Wir suchen zum nächstmöglichen Zeitpunkt für unser Büro in Basel und unsere Projektstandorte in der Deutschschweiz einen Projektingenieur (m/w) - Vollzeit (100%) Leidenschaft für Pharma Engineering. Gegründet und entwickelt von zwei namhaften Pharmaunternehmen, können wir mit Stolz feststellen, dass alle regulatorischen und sonstigen spezifischen Anforderungen dieser Branche Teil..... klicken sie bewerben, für die volle Stellenbeschreibung

Wir suchen zum nächstmöglichen Zeitpunkt für unseren Standort Basel einen Ingenieur HLKK (Versorgungstechnik / Gebäudetechnik) (m/w) - Vollzeit (100%) Leidenschaft für Pharma Engineering. Gegründet und entwickelt von zwei namhaften Pharmaunternehmen, können wir mit Stolz feststellen, dass alle regulatorischen und sonstigen spezifischen Anforderungen dieser Branche Teil unserer DNA..... klicken sie bewerben, für die volle Stellenbeschreibung

Wir suchen zum nächstmöglichen Zeitpunkt für unser Büro in Basel und unsere Projektstandorte in der Deutschschweiz einen Qualifizierungs- / Validierungs-Projektingenieur (m/w) - Vollzeit (100%) Leidenschaft für Pharma Engineering. Gegründet und entwickelt von zwei namhaften Pharmaunternehmen, können wir mit Stolz feststellen, dass alle regulatorischen und sonstigen spezifischen..... klicken sie bewerben, für die volle Stellenbeschreibung

Das kannst du bewirken: Du bist für die umfassende Beratung sowie den Verkauf unserer vielseitigen Produkte und Dienstleistungen verantwortlichDie bestehende Kundschaft entwickelst du mit Leidenschaft weiter, du führst Beratungen durch und repräsentierst PostFinance an KundeneventsDu hilfst mit, die Anlagegeschäfte bei PostFinance zu pushen und im Markt zu platzierenUnsere Kundinnen und Kunden begleitest du in die Digitalisierung und unterstützt sie auf dem Weg zur Nutzung der digitalen AngeboteDank deinem Drive und hohe Selbständigkeit, erreichst du die vereinbarten Verkaufs- und Entwicklungsziele mit Leichtigkeit und leistest deinen essenziellen Beitrag zum Erfolg von PostFinance, Das bringst du mit: Du bist Kauffrau/-mann EFZ oder hast eine Ausbildung im Verkauf abgeschlossen und bringst zusätzlich eine Weiterbildung im Finanzbereich mitDeine mehrjährige Erfahrung in der Kundenberatung im Finanz- oder Versicherungsbereich verbunden mit deiner ausgesprochen hohen Kundenorientierung und Freude an der telefonischen und persönlichen Kundengewinnung zeichnen dich ausDas Anlagegeschäft ist dein Business, du bringst von Vorteil bereits Erfahrung in diesem Bereich mitDu trittst überzeugt auf, steckst Kundinnen und Kunden mit deiner Begeisterung an und bietest ihnen ein herausragendes ErlebnisDeutsch beherrschst du einwandfrei, gute Französisch- und Englischkenntnisse runden dein Profil ab

Standorte: Basel (CH) Answers to Automation. Process Automation Solutions ist einer der führenden, herstellerunabhängigen Anbieter von kompletten Automatisierungslösungen für die Prozess- und Fertigungsindustrie. Wir beschäftigen aktuell 1.410 Mitarbeiter in Europa, Amerika und Asien. Schwerpunkte unserer Tätigkeit sind die Projektierung von Steuerungs- und..... klicken sie bewerben, für die volle Stellenbeschreibung

CSV Consultant - Basel Jocelyn Blackham is recruiting for a CSV Consultant to join a company in the drug discovery industry at their site based in Basel on a 6-contract basis. The main purpose of the role will be to: - Provide assurance that GxP regulated computerized systems are suitably implemented and managed in accordance with the company's requirements and, where appropriate, in accordance with regulatory requirements. - Deliver support, guidance and advice with regard to computerized system validation within GxP area, 21 CFR Part 11 and EU GMP Annex 11. - Offer support, guidance and advice with regard to IT Infrastructure qualification to comply with GxP requirements. Further responsibilities will include: - Determining regulations that are applicable to a computerized system and need for validation. - Applying advanced knowledge and experience to address complex issues. - Acting as a primary contact person between the computerized system project team and Pharmaceutical Development Department. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Good knowledge and understanding of regulatory requirements such as GxP & 21 CFR Part 11 and GAMP5 guidelines, EU GMP Annex 11. - Solid experience in Computerized Systems Validation (CSV). - University degree with suitable qualification in the pharmaceutical industry area. This is an excellent opportunity to join a growing company in the pharmaceutical industry. Please could you send any correspondence in English. Please quote reference 45945 in all correspondence.

CSV Consultant - Basel Jocelyn Blackham is recruiting for a CSV Consultant to join a company in the drug discovery industry at their site based in Basel on a 6-contract basis. The main purpose of the role will be to: - Provide assurance that GxP regulated computerized systems are suitably implemented and managed in accordance with the company's requirements and, where appropriate, in accordance with regulatory requirements. - Deliver support, guidance and advice with regard to computerized system validation within GxP area, 21 CFR Part 11 and EU GMP Annex 11. - Offer support, guidance and advice with regard to IT Infrastructure qualification to comply with GxP requirements. Further responsibilities will include: - Determining regulations that are applicable to a computerized system and need for validation. - Applying advanced knowledge and experience to address complex issues. - Acting as a primary contact person between the computerized system project team and Pharmaceutical Development Department. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Good knowledge and understanding of regulatory requirements such as GxP & 21 CFR Part 11 and GAMP5 guidelines, EU GMP Annex 11. - Solid experience in Computerized Systems Validation (CSV). - University degree with suitable qualification in the pharmaceutical industry area. This is an excellent opportunity to join a growing company in the pharmaceutical industry. Please could you send any correspondence in English. Please quote reference 45945 in all correspondence.

QA Manager Drug Product - Basel Jasmin Baumgartner is recruiting for a QA Manager Drug Product to join a company in the drug discovery industry at their site based in Basel on a contract basis of 12 months. The main purpose of the role will be to: - Deliver GMP/GDP expertise therefore ensuring that medicinal products are developed, manufactured, packed, labelled, distributed and controlled in accordance with regulatory expectations and applicable quality standards. - Complete GMP on site audits at Contract Manufacturing Organizations (CMOs). - Prepare GMP/GDP Agreements in collaboration with CMOs and the CMC team. Further responsibilities will include: - Establishing a quality risk management approach in projects based on ICH Q9 concepts to ensure that quality is understood and managed by all stakeholders throughout the product life cycle. - Performing QA activities to support release of active ingredients, investigational medicinal products including approval of master process documentation, batch record review, resolution of investigations, and assessment of change controls. - Preparing, reviewing, and/or approving internal SOPs and other GMP/GDP related documentation. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Advanced University degree in Pharmacy, Chemistry or alternative technical/science university degree. - Excellent knowledge and experience in different positions like pharmaceutical or chemical development, quality control, analytical development, chemical or pharmaceutical production or comparable operational positions in the pharmaceutical industry. - Prior experience in quality assurance of drug product covering also combination products is essential. This is an excellent opportunity to join a growing company in the pharmaceutical branch. Please quote reference 45878 in all correspondence.

QA Manager Drug Product - Basel Jasmin Baumgartner is recruiting for a QA Manager Drug Product to join a company in the drug discovery industry at their site based in Basel on a contract basis of 12 months. The main purpose of the role will be to: - Deliver GMP/GDP expertise therefore ensuring that medicinal products are developed, manufactured, packed, labelled, distributed and controlled in accordance with regulatory expectations and applicable quality standards. - Complete GMP on site audits at Contract Manufacturing Organizations (CMOs). - Prepare GMP/GDP Agreements in collaboration with CMOs and the CMC team. Further responsibilities will include: - Establishing a quality risk management approach in projects based on ICH Q9 concepts to ensure that quality is understood and managed by all stakeholders throughout the product life cycle. - Performing QA activities to support release of active ingredients, investigational medicinal products including approval of master process documentation, batch record review, resolution of investigations, and assessment of change controls. - Preparing, reviewing, and/or approving internal SOPs and other GMP/GDP related documentation. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Advanced University degree in Pharmacy, Chemistry or alternative technical/science university degree. - Excellent knowledge and experience in different positions like pharmaceutical or chemical development, quality control, analytical development, chemical or pharmaceutical production or comparable operational positions in the pharmaceutical industry. - Prior experience in quality assurance of drug product covering also combination products is essential. This is an excellent opportunity to join a growing company in the pharmaceutical branch. Please quote reference 45878 in all correspondence.

Senior QA Manager Drug Substance (GMP/GDP) - Basel, Switzerland Jocelyn Blackham is recruiting for a Senior QA Manager Drug Substance (GMP/GDP) to join a rapidly growing company in the drug discovery area. The position will be offered on a 6-12 month contract at our clients site in Basel, with the possibility of extension. The main purpose of the role will be to: - Provide GMP/GDP quality assurance expertise during development and later during commercialization of products. - Perform GMP onsite audits at Contract Manufacturing Organizations (CMOs). - Prepare GMP/GDP Agreements in collaboration with CMOs and the CMC team. - Write, review, and/or approve internal SOPs and other GMP/GDP related documentation. - Ensure that medicinal products are designed, developed, manufactured and controlled according to quality standards. - Establish a quality risk management approach in projects based on ICH Q9 concepts to ensure that quality is understood and managed by all stakeholders throughout the product life cycle. - Manage all required activities to support release of active ingredients, investigational medicinal products including approval of master process documentation, batch record review, resolution of investigations, and assessment of change controls. Further responsibilities will include: - Notifying management of potential quality and regulatory issues. - Providing guidance on the resolution of complaints, testing issues, discrepancies and Out of Specifications, investigations and Corrective and Preventive Actions as needed, on assigned projects. - Supporting the review and optimization of the company's pharmaceutical quality system by establishing and preparing review of relevant Key Performance Indicators. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Advanced University degree in Pharmacy, Chemistry or alternative technical/science university degree. - Previous experience in different positions like pharmaceutical or chemical development, quality control, analytical development, chemical or pharmaceutical production or similar operational positions in the pharmaceutical industry. - Previous experience in quality assurance activities specific to drug substance. - Excellent knowledge of GMPs and regulatory environments, ability to interpret and implement quality standards. - Strong interpersonal and influencing skills. - Entrepreneurial mind set combined with cost consciousness. This is an excellent opportunity to join a expanding pharmaceutical company. Please quote reference 45874 in all correspondence.

Über uns Wir sind uns bewusst, wie wichtig es ist, medizinische Lösungen heute zur Verfügung zu stellen und gleichzeitig Innovationen für morgen zu entwickeln. Wir arbeiten mit Leidenschaft daran, die Gesundheit und das Leben von Patientinnen und Patienten zu verbessern. Wir zeigen Mut in unseren Entscheidungen und in unserem Tun. Und wir sind davon überzeugt, dass gutes und erfolgreiches Handeln zu einer besseren Welt beiträgt. Das ist der Grund, warum wir täglich zur Arbeit kommen. Wir fühlen uns der Wissenschaft verpflichtet, setzen höchste ethische Maßstäbe und bekennen uns zum Zugang zu medizinischen Innovationen für alle. Wir tun dies, um an einer besseren Zukunft mitzuwirken. Wir sind stolz darauf, wer wir sind, was wir leisten und wie wir dabei vorgehen. Wir sind viele und arbeiten Hand in Hand - über Funktionen, Standorte und Länder hinweg. Wir sind Roche. ​ Postdoctorate Modeling and Simulation Scientist (2 years) Basel Vollzeit 20160 Who we are: At Roche, 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we've become one of the world's leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each other's differences as an advantage. To innovate healthcare, Roche has ambitious plans to keep learning and growing - and is seeking people who have the same goals for themselves. At Roche, we believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives and we are fearless in both decision and action. And we believe that good business means a better world. That is why we come to work every single day. We commit ourselves to scientific rigour, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. The Position: The Translational Modeling and Simulation Group is part of the Pharmaceutical Sciences department, focused on quantitative preclinical modeling and simulation. We are looking for an outstanding, hardworking, highly motivated individual to join our team as a Postdoctoral Research Fellow. In this role, you will integrate data from multiple sources with the goal of developing predictive mathematical, statistical and/or machine-learning models of immunogenicity in the context of drug development. The Roche Postdoctoral Fellowship (RPF) program is sought at supporting excellent early-career scientists focusing on collaborative R&D projects between Roche and international academic institutions. Both internal Roche and external academic experts will act as mentors, and you will be based primarily at Roche Innovation Centre Basel, Switzerland. In this position you will: Develop modeling and simulation tools to support research in the area of immunogenicity Integrate data from multiple sources (in-vitro, in-vivo, clinical) to generate and test hypotheses for prediction of immunogenicity incidence, management and prevention Publish your findings in high-impact journals Who you are: A highly motivated scientist with strong experience in modeling and simulation and excellent communication skills, who enjoys working in multidisciplinary and multinational teams Someone who enjoys and has experience in creative, data-driven quantitative modeling Requirements: PhD in mathematics, physics, engineering, statistics, biostatistics, modelling and simulation or a related discipline with no more than 4 years of work experience since graduation. Strong knowledge of programming in Matlab, R, Python (other languages a plus). Substantial track record of scientific publications as journal articles and conference talks Fluency in written and spoken English Experience in machine learning and knowledge of basic immunology would be a plus

Join our Scientific Communications Director Talent pool for Switzerland! Basel Über uns Wir sind uns bewusst, wie wichtig es ist, medizinische Lösungen heute zur Verfügung zu stellen und gleichzeitig Innovationen für morgen zu entwickeln. Wir arbeiten mit Leidenschaft daran, die Gesundheit und das Leben von Patientinnen und Patienten zu verbessern. Wir zeigen Mut in unseren Entscheidungen und in unserem Tun. Und wir sind davon überzeugt, dass gutes und erfolgreiches Handeln zu einer besseren Welt beiträgt. Das ist der Grund, warum wir täglich zur Arbeit kommen. Wir fühlen uns der Wissenschaft verpflichtet, setzen höchste ethische Maßstäbe und bekennen uns zum Zugang zu medizinischen Innovationen für alle. Wir tun dies, um an einer besseren Zukunft mitzuwirken. Wir sind stolz darauf, wer wir sind, was wir leisten und wie wir dabei vorgehen. Wir sind viele und arbeiten Hand in Hand - über Funktionen, Standorte und Länder hinweg. Wir sind Roche. ​ If you would like to join us and to be considered as a potential candidate in order to make a difference, please join our Scientific Communications Talent pool for Switzerland! Have you already reviewed our current open vacancies? If you find a position that meets your requirements, please submit your application via our careers portal. Scientific Communications Job Openings Are there currently no positions matching your requirements? Don't worry, you can still submit your application proactively for the following position: EXPERIENCED Scientific Communications Director (M/F) As a Scientific Communications Director, you sit at the heart of Roche's Global Product Development Medical Affairs organization. In PDMA we are passionate about developing and driving an industry leading medical strategy in close collaboration with our cross-functional stakeholders and affiliate partners - we are enthusiastically committed towards our Medical Affairs vision: Transforming clinical practice. The objectives and scope of the position will be to: Develop and implement the integrated Scientific Communications Strategy (iCS) for the assigned molecule Bring consistency across execution, assessment, and amplification across all Scientific Communication activities for the assigned molecule and drives excellence and innovation in these areas (e.g. Medical Education, Publications, Congress strategy, etc) Act as a strategic partner to US Medical Affairs responsible for the US focused publication strategy and implementation for the respective molecule Stay abreast of internal and external developments, trends and other dynamics relevant for the assigned molecule to maintain a fully current view and perspectives of external influences Minimum Requirements: Advanced degree (PhD) and/or certification in a scientific medical field preferred Professional experience in the pharmaceutical/ biotechnology industry or related experience - especially medical affairs, clinical development or medical communications experience Fluent in English (oral and written Excellent communications and interpersonal skills, team-oriented Quality and focus oriented We are regularly looking for Scientific Communications Directors (M/F) in the following therapeutic areas: Ophthalmology, Oncology & Neuroscience Personalized Healthcare