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Pharmazie: 34 Jobs in Kirchheim bei München

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Pharmazie

Senior Manager CMC Regulatory Affairs (m/f/x)

Sa. 04.12.2021
München
Daiichi Sankyo is dedicated to creating new modalities and innovative medicines by leveraging our world-class science and technology for our purpose “to contribute to the enrichment of quality of life around the world”. In addition to our current portfolio of medicines for cancer and cardiovascular disease, Daiichi Sankyo is primarily focused on developing novel therapies for people with cancer as well as other diseases with high unmet medical needs. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation to realize our 2030 Vision to become an “Innovative Global Healthcare Company Contributing to the Sustainable Development of Society”. For our headquarter in Munich we are seeking highly qualified candidates to fill the position: Senior Manager CMC Regulatory Affairs (m/f/x) The Senior Manager Regulatory Affairs CMC will provide European regulatory CMC guidance and strategy for assigned products and will represent Regulatory Affairs CMC EU in internal and external interactions (e.g. global and local project teams, working teams, authorities interactions (Scientific Advice), CMOs). The function will support or lead the preparation of regulatory CMC documents during development and life cycle management in a manner that is scientifically sound, commercially viable and in accordance with regulatory CMC standards. He/She may act as a specialist for biological products in the EU regulatory CMC field. The function communicates EU and international regulatory requirements to authoring teams, develop the EU regulatory strategies and review dossiers and technical documents. The function and the team collaborates companywide within the global RACMC department and technical functions. The function is proactively influencing the internal, but also external regulatory affairs environment. Roles and responsibilities: Working in regulatory teams to conduct preparation of M2 and M3 CTD documents for EU MAAs and IMPDs filings of new drugs, incl. Quality Overall Summary (QOS) Represent EU RACMC function in global RACMC and CMC development teams and provide CMC regulatory guidance and strategy Review CMC documents, develop regulatory strategies, provide risk assessments Support the preparation and execution of Health Authority meetings Interpret, develop strategy and lead response preparation on Health Authorities information requests Keep close collaboration with global RACMC colleagues and technical experts, across all regions Keep current with, review and interpret regulatory and scientific regulations, directives, guidelines and initiatives, communicate important changes and trends with the relevant stakeholders Participate or lead assigned non-project tasks and process improvements Ensure maintenance of the regulatory compliance Master degree in Life Science or Pharmacy, PhD preferred; Master Degree in Regulatory Affairs is a plus Minimum of 5 years of experience in the pharmaceutical industry Minimum of 3 years of experience in global regulatory affairs CMC with emphasis on late stage CMC drug development and marketing authorization applications in Europe; experience in the development of biologics preferred Proven ability to plan, coordinate and lead activities simultaneously on multiple projects Excellent personal and intercultural skills paired with the ability to work cross functionally in a multinational organisation Experience of working in global environment in interdisciplinary teams Experience of working in or leading interdisciplinary teams Solution and detail-oriented; well organised and self-motivated Excellent written and oral communication skills in English, German as a second language preferred Strong working knowledge of Microsoft Office We offer an interesting, diversified and challenging position, good contractual conditions, flexible working models, all the social benefits of a modern company and a professional environment where you will have the opportunity for personal growth.
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Senior Manager Regulatory Affairs Oncology (m/f/x)

Sa. 04.12.2021
München
Daiichi Sankyo and its 16,000 employees in more than 20 countries are dedicated to the creation and supply of innovative pharmaceutical products. In Europe, we focus on two areas: In the cardiovascular space, our strong portfolio of medicines reflects our long-standing commitment and shows that we care for every heartbeat; in oncology our goal is to become a global pharma innovator until 2025 by providing novel therapies to patients across the world. Our European headquarters are in Munich, Germany, and we have affiliates in 13 European countries. For our Headquarter in Munich we are seeking two highly qualified candidates to fill the position: Senior Manager Regulatory Affairs Oncology (m/f/x) To provide European regulatory strategy support for assigned projects, products and non-project work. Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as a member of a multi-disciplinary team, providing expertise on regulatory matters. Represent Regulatory Affairs in external interactions (e.g. authorities, affiliates, partners, CROs) providing expertise on regulatory strategy to achieve regional and global goals. Role and Responsibilities European regulatory strategy support for assigned projects, covering product development plans, clinical trials and Marketing Authorizations Applications (MAA) as well as product life cycle management. European Regulatory Affairs representation on global development teams providing regulatory guidance and strategy and supporting EU MAA submissions Act as regulatory contact person for authorities for assigned projects Participate in assigned non-project tasks and process improvements Keep current with, review and interpret regulatory and scientific regulations, directives, guidelines and initiatives, communicate important changes and trends with the relevant stakeholders Bachelor degree in Life Science or Medical Science; Degree in Pharmacy, Master and/or PhD preferred; Master Degree in Regulatory Affairs is a plus Minimum of 8 years of experience in the pharmaceutical industry and minimum of 5 years of experience in global regulatory affairs with emphasis on late stage drug development and marketing authorization applications in Europe, experience with clinical trials, orphan drugs and pediatric clinical development Experience of working in global environment as well as with National Health Agencies and EMA Proven ability to plan, coordinate and lead activities simultaneously on multiple project Excellent personal and intercultural skills paired with the ability to work cross functionally in a multinational organisation Ability to develop and maintain good relationships, challenge views, present and argue cases in a professional and respectful manner Solution and detail-oriented; well organised and self-motivated Excellent written and oral communication skills in English, second language preferred Competitive Pay Work-Life-Balance Growth and Development Health and Family Working at Daiichi Sankyo: At Daiichi Sankyo in Europe, we offer a workplace where your voice is heard. Everything we do, we do with a high level of commitment and a clear focus on patients’ needs. We know that our bold ambition to change patients’ lives for the better can only be achieved through the power of collaboration and the exploration of new approaches. Thus, we encourage our colleagues across Europe to be courageous, to bring their ideas to the table and to embrace opportunities to grow. When you join our European family, you will be a part of a dynamic company where everyone, no matter their role, rolls up their sleeves and gets things done.
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Personalreferent (m/w/d) mit Schwerpunkt Recruiting

Fr. 03.12.2021
Martinsried
Proteros is a privately held early-stage services provider in structure-based drug discovery with a cutting-edge discovery engine tailored to unlock even the most technically challenging targets. Proteros’ work is built on scientific excellence and supports its clients to reach the right results and accelerate their overall research timelines. Proteros supports most of the world’s 20 largest pharma companies and more than 250 pharmaceutical and biotech partners in the US, Europe and Japan. For more information please visit www.proteros.com. SENIOR PROJECT MANAGER (M/F/D) IN EARLY STAGE DRUG DISCOVERY Project Management of Discovery Solutions (Early Stage Drug Discovery) and Structural Biology projects within the scope of our business approach, including customer interaction with international Pharma and Biotech companies in the US and EU Acquisition of Early Drug Discovery Projects Lead multi-disciplinary scientific teams Suggest suitable solutions and technological approaches according to target/customer needs Drive projects from gene to qualified hits according to research target profile (RTP) including mode of inhibition/action, biophysical validation and structures Hands-on experience in industrial drug discovery, including protein sciences, biophysical/biochemical assays, and structural biology Prior minimum of 2-years experience in pharma, biotech, CRO, or academia in Biophysics/Structural Biology PH.D. degree in in Biochemistry, Molecular Biology, Biophysics, Structural Biology, Medicinal Chemistry, or related fields, post-doc experience Good understanding of small molecule drug discovery processes including enabling technologies in the areas of protein sciences, structural biology, and biophysical/biochemical assays and Hit identification Ability to manage multiple complex projects simultaneously with internal and external stakeholders and eagerness to move projects to completion Able to envision a project as a “whole package”, anticipate problems/bottlenecks, and mitigate risks Service mindset Excellent written, verbal and interpersonal communication skills and the ability to effectively interact with all levels both within and outside the company Demonstrated strong sense of responsibility and collaboration, and excellent analytical skills an innovative profession in an exciting industry an inspiring working atmosphere as fertile ground for your further development a comprehensive training that prepares you optimally for your area of responsibility multicultural teams and an open corporate culture
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Pharmazeutischer Mitarbeiter PTA / PKA (m/w/d) 2nd Level Support

Fr. 03.12.2021
Fürth, Bayern, München, Nürnberg, Stuttgart
Werden Sie ALL IN! for Health als Pharmazeutischer Mitarbeiter PTA / PKA (m/w/d) 2nd Level Support Die Entwicklung von innovativen und intelligenten Lösungen für den effizienten Ablauf im Apothekenalltag ist unsere Mission! Wir stehen dazu in direktem Austausch mit unseren Kunden, um unsere Produkte fortlaufend zu optimieren. Unsere Hard- und Softwareprodukte bieten Apotheken Zuverlässigkeit und Sicherheit - genau wie unsere Mitarbeitenden, die Ihr Fachwissen verantwortungsvoll einsetzen. Werden Sie jetzt Teil unseres Teams! Ihr Beitrag: Sie bearbeiten telefonisch und schriftlich die Anfragen aus unserem 1st Level Support und geben weiterführende Hilfestellung sowie Lösungen Sie übernehmen komplexe Anfragen und unterstützen unsere Kunden bei Fragen zu unserem Warenwirtschaftssystem WINAPO®, unseren Betriebssystemen und unserer Hardware Sie dokumentieren Ihre Tätigkeiten über SAP-CRM und verarbeiten Ihre Lösungsansätze z. B. in Form von F.A.Q. Einträgen Im Rahmen der Produktverbesserung und bei speziellen Anliegen arbeiten Sie eng mit anderen Fachabteilungen zusammen, z. B. in der Testung und Dokumentation von Programmfunktionen Das bringen Sie mit: Sie verfügen über eine abgeschlossene Ausbildung im pharmazeutischen Bereich, z. B. als Pharmazeutisch-technischer Assistent (m/w/d), Pharmazeutisch-kaufmännischer Angestellter (m/w/d), oder bringen eine gleichwertige Qualifikation mit Sie besitzen gute IT-Kenntnisse (Excel/ Word) und haben idealerweise bereits Erfahrung im Gesundheitswesen Sie arbeiten gerne im Team und zeichnen sich durch Ihre selbständige und lösungsorientierte Arbeitsweise aus Das können Sie von uns erwarten: Einen sicheren digitalen Bewerbungs- und Onboarding-Prozess während der COVID-19 Pandemie Einen krisensicheren und unbefristeten Arbeitsplatz Ein ausgereiftes Service- und Supportkonzept leistet Ihnen umfangreiche Unterstützung Vielfältige Weiterentwicklungsmöglichkeiten und langfristige Perspektiven innerhalb unseres wachsenden Unternehmens Digitales Feel Good Management mit vielfältigen Angeboten für Ihre Gesundheit, z. B. Home-Workouts, Ernährungsberatung, Mentaltrainings, etc. Moderne Arbeitsplätze, Vertrauensarbeitszeit, Mobiles Arbeiten, Mitarbeiterrabatte, u. v. m. sorgen für ein angenehmes Arbeitsumfeld Überzeugt? Bewerben Sie sich online mit Ihren aussagekräftigen Bewerbungsunterlagen (inkl. Gehaltsvorstellung und nächstmöglichen Eintrittstermin). Synchronizing Healthcare Werden Sie ALL IN! mit Kopf, Herz und Hand
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Clinical Development Scientist (f/m/d)

Do. 02.12.2021
Garching bei München
ITM is a privately owned biotechnology and radiopharmaceutical group of companies dedicated to the development, production and global supply of targeted diagnostic and therapeutic radiopharmaceuticals and radioisotopes for use in cancer treatment. We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuroendocrine cancers or bone metastases. Our main objectives are to significantly improve treatment outcomes and quality of life for cancer patients through a new generation of Targeted Radionuclide Therapies in Precision Oncology. The headquarters are located in the heart of the research center of the Technical University of Munich (TUM).Reporting to the Head of Clinical Development, in his / her position the Clinical Development Scientist (f/m/d) will help the Medical Leads in managing the scientific and medical activities of the different projects in close collaboration with external sub-contractors (CROs), internal and external experts as well as all ITM departments (Regulatory Affairs, Clinical Operations, R&D and Medical Affairs etc.). Support the project Medical Lead(s) Contribute from study strategy and design, protocol concept to data analysis, interpretation and final study report to deliver the clinical development activities which ensure consistency with the clinical development strategy Appropriately interact with Key Opinion Leaders (KOLs), collaborators, CROs, advisory boards, DSMB etc. Contribute to the medical monitoring and data cleaning of ongoing studies Ensure that high quality documents (protocols, IBs, ICFs etc.) are developed aligned to the Clinical Development Plan to effectively determine a medicine's potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe Participate in eCRF development Participates in data review ongoing through study including interim analyses, in-stream data review etc. Present the scientific rationale and study design at Investigator Meetings and respond to scientific questions arising from sites during study conduct Ensure prompt, quality communications with sites regarding protocol clarification and procedural queries Implement new business processes and strategies and also proactively identify issues and propose strategies to manage implications and risks on clinical study / Clinical Development plan Contribute to documents for regulatory submissions and advisory requirement, including scientific advice, IND / CTA, and NDA / BLA / MAA Contribute to all regulatory reporting requirements (e.g., DSUR, INDSRs etc.) Ensure prompt, quality responses to Regulatory Agencies, Institutional Review Boards (IRB) / Ethics Review Committees (ERC), Independent Data Monitoring Committees (IDMC) etc. Deliver of end-of-study reports and publication/presentation of results Advanced life science degree (PhD, preferably MD) Ability to work in a hierarchically flat, matrix environment Ideally a minimum of one to two years of professional experience as clinical scientist in a drug / biologic developing company, ideally in oncology indication Strong working knowledge of the clinical drug development process, clinical trial design, medical monitoring, data management (including CDISC standards) and biostatistics Ability to understand, integrate, analyse and interpret clinical data Fluency in English Good management, interpersonal, communication, negotiation and problem-solving skills A modern workplace and exciting opportunities in an evolving and fast growing company Challenging and varied projects in interdisciplinary, multicultural and highly professional teams A collegial corporate culture and short communication channels Flexible working hours with an attractive salary package and diverse corporate benefits
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Head of Quality Management (m/w/d)

Do. 02.12.2021
Ottobrunn
Minaris Regenerative Medicine GmbH ist ein globaler Partner für Auftragsforschung und Lohnherstellung. Wir produzieren hochmoderne Zell- und Gentherapien nach den Vorgaben der Guten Herstellungspraxis (GMP) für die Anwendung im Menschen. Bei uns tragen Sie aktiv zum medizinischen Fortschritt bei und geben schwer kranken Patienten Hoffnung. Weitere Informationen finden Sie auf unserer Webseite rm.minaris.com. Unter „Bewerben“ können Sie mit nur wenigen Klicks Ihren Lebenslauf hochladen. Wir freuen uns auf Sie! Zur Verstärkung unseres Management Teams am Standort Ottobrunn suchen wir eine/n: Head of Quality Management (m/w/d) Strategische wie operative Weiterentwicklung des GMP konformen Qualitätsmanagementsystems für die Herstellung von Zell- und Gentherapeutika (ATMP’s) Prozessverantwortung für sämtliche Prozesse des QM-Systems Sicherstellung und Optimierung der Schnittstellen des Qualitätsmanagements zu benachbarten Abteilungen Planung, Vorbereitung und Durchführung von (internationalen) Kundenaudits und Behördeninspektionen Durchführung von Audits für die Qualifizierung von Lieferanten und Prüflaboren Führen, Fördern und Weiterentwickeln der Mitarbeiter im Verantwortungsbereich Verantwortliche Erstellung des jährlichen Budgets einschließlich Personalplanung und Investitionen für den eigenen Bereich Abgeschlossenes pharmazeutisches oder naturwissenschaftliches Studium oder vergleichbare Qualifikation Mehrjährige Berufserfahrung in der Ausübung der Tätigkeit als Leiter der Qualitätssicherung oder -kontrolle im Bereich der Arzneimittelherstellung oder -prüfung oder vergleichbare Qualifikation Erfahrung im Bereich der Arzneimittel für neuartige Therapien (Advanced Therapy Medicinal Products, ATMPs) wünschenswert Hohe fachliche Kompetenz und tiefe Kenntnis der gesetzlichen Vorschriften im Bereich Arzneimittelherstellung, -prüfung und -freigabe Mehrjährige Erfahrung in der Analytik gemäß § 15 AMG im Hinblick auf eine mögliche Erlangung der Sachkenntnis zur Sachkundigen Person gemäß § 14 AMG von Vorteil Führungsexpertise und damit verbunden die Fähigkeit, Ihr Team zu fördern und zu motivieren um Höchstleistungen im Sinne der vereinbarten Ziele in einem dynamischen Umfeld zu erbringen Flexibilität, Lösungsorientierung und Prozessaffinität und ein ausgeprägtes Maß an Qualitäts-, Kunden- und Zielorientierung Verhandlungssichere Englischkenntnisse in Wort und Schrift sowie gute IT-Kenntnisse Ein starkes Team, das zum medizinischen Fortschritt beiträgt Ein spannendes und innovatives Umfeld mit zahlreichen Gestaltungs- und Entwicklungsmöglichkeiten Teil des japanischen Konzerns Showa Denko Materials Co., Ltd 13 Gehaltszahlungen Betriebliche Altersvorsorge, Vermögenswirksame Leistungen Zuschuss zur Kinderbetreuung Diverse Mitarbeitervergünstigungen
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Global Patient Safety (GPS) Senior Scientist (gn)

Do. 02.12.2021
Planegg
MorphoSys’ mission is to make exceptional, innovative biopharmaceuticals to improve the lives of patients suffering from serious diseases. Innovative technologies and smart development strategies are central to our approach. Success is created by our people, who focus on excellence in all they do, collaborate closely across disciplines. We all are driven by a desire to make the medicines of tomorrow a reality. Guided by mutual respect and trust, each member of the MorphoSys team is given the opportunity to develop and flourish within this exciting and inspiring environment. Join us in Planegg near Munich! We would like to fill the following vacancy as soon as possible: Global Patient Safety (GPS) Senior Scientist (gn) You will be a core member of the relevant product-specific Safety Management and Review Team(s) (SMART) Provide technical safety expertise to ensure the scientific integrity and quality of all relevant safety-related clinical development and post-marketing activities and deliverables Responsible for but not exclusively: All relevant safety-related clinical trial activities and deliverables, including writing relevant sections of clinical trial protocols and related documents (member of the respective cross-functional Clinical Trial Teams) Safety signal management Benefit-risk evaluations Definition and implementation of pharmacovigilance and risk minimisation activities Health Hazard Evaluations for Product Quality Concerns Responses to safety-related questions from health authorities Provide state-of-the-art safety scientific methodology for safety data analysis, visualization and interpretation, collaborating closely with biostatistical colleagues Provide technical / scientific expertise to the development and implementation of new tools, e.g. safety data analysis and visualization tools Present safety-related data, information and messages to internal and external audiences as required Demonstrate knowledge of, and ensure compliance with company guidelines, policies and procedures and be able to demonstrate this during health authority inspections A higher qualification (Masters degree or PhD or equivalent) in a bioscience subject, or pharmacy Professional Experience: Good understanding of the pharmaceutical industry Sound knowledge and understanding of industry and pharmacovigilance legislation, including ICH-GCP and clinical safety guidelines, EU Clinical Trials Regulation and EMA GVP Modules, and FDA clinical safety and risk management guidance, and the need for compliance with these Extensive experience in pharmacovigilance/patient safety, plus / minus clinical research Close cross-functional collaboration, including with Biostatistics, Regulatory Affairs, Clinical Development, Medical Affairs, C&QA, Non-clinical drug safety, CMC Personal Skills: Fluent spoken and written professional English Excellent communication skills, oral and written – ability to present information clearly and concisely Strong team-working skills – working across cultural and functional boundaries Able to prioritise, adapt rapidly to changes in priorities, and manage multiple situations / issues, remaining calm and delivering under pressure Strategic thinking Problem-solving and decision-making ability Creative working in X-functional teams Open and appreciative corporate culture Multicultural environment Working in an attractive, high-quality equipped building with restaurant Free sports and language courses
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Project Manager (f/m/d) Drug Product Development for Biopharmaceuticals

Do. 02.12.2021
München
Coriolis Pharma is a globally operating independent service provider for formulation research and development of for a large variety of different (bio)pharmaceutical molecules, including proteins, peptides, nucleic acids, ATMPs (in particular viral vectors for gene delivery), GMOs, vaccines and virus(-like) particles. An interdisciplinary team of highly qualified scientists with many years of experience in the development of (bio)pharmaceuticals supported by an expert scientific advisory board provides cutting-edge service and know-how related to the formulation development of biopharmaceuticals. At our company, we pursue one goal every day: the advancement of medicines to cure people. Our expanding company currently employs about 140 people at two sites. For our Team in Munich we are currently looking for Project Manager (f/m/d) Drug Product Development for Biopharmaceuticals Take over the responsibility to lead and manage drug product development projects with focus on formulation development (liquid and/or lyophilized) for biopharmaceuticals and vaccines for clients Take over the lead in the communication with the client (first point of contact) and internally with other project team members and involved units at Coriolis Ensure that relevant resources are embedded into the project and that project-related decisions are based on state-of-the-art scientific principles Perform project planning, coordination, execution (supported by project team members for laboratory work) and resource management Ensure timely delivery of projects within budget, scope and desired quality Ensure that project deliverables, i.e. experimental plans, experimental data, data presentations and reports are prepared timely and according to the required quality standards Take over the responsibility for interpretation of data and the drawing of final conclusions; compile data presentations and reports Act in the role as a drug product development expert (individually with a different focus based on your experience) and provide support to scientists and junior scientists University degree in pharmacy, (bio)chemistry, biology, or related field, PhD beneficial A mininum of 4-5 years of relevant working experience Proven ability in leading drug product development programs Profound expert / scientific knowledge in liquid and/or lyophilization formulation development and analytical characterization of biophamaceuticals Team player with strong motivation and inter-personal skills Open for new ideas and tasks, can-do attitude and hands on mentality Excellent verbal and written communication skills in English and German As a Project Manager, you will join a highly motivated, interdisciplinary team performing contract research and development for clients from the (bio)pharmaceutical industry worldwide. We offer you diversified and challenging areas of responsibilities in our innovative company. We actively support your personal development (project management, technical, scientific and personal skills) tailored to your individual development plan. Beyond that Coriolis offers a variety of benefits and team activities to its employees. Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, sex, gender, color, disability, religion/belief, sexual orientation, marital status  or age.  We value diversity at our company! Due to the current events concerning COVID-19, Coriolis Pharma has implemented different measures to ensure the health and safety of our employees (Air filter in every office, free masks and disinfectants, flexible use of home office).
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Trainerin für Apothekenpersonal (m/w/d) PTA im Schulungsaußendienst

Do. 02.12.2021
Frankfurt am Main, Mainz, Karlsruhe (Baden), Kassel, Hessen, Mannheim, München, Nürnberg, Saarbrücken, Stuttgart
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. IQVIA has 80,000 employees in more than 100 countries, all committed to making the potential of Human Data Science a reality.Join us on our exciting journey! Trainerin für Apothekenpersonal (m/w/d)PTA im Schulungsaußendienst Du bist Berater mit Leib und Seele und kommst aus dem Apothekenumfeld? Du möchtest Wissen weitergeben und liebst es, zu inspirieren? Dann bist Du bei Aposphäre, dem führenden Apothekenschulungsaußendienst, genau richtig! Als innovativer Partner der Pharmaindustrie unterstützen wir Apotheken bei sämtlichen Herausforderungen am Point of Sale – von kreativen Maßnahmen für mehr Abverkauf bis zu intensiven Schulungen und Coachings zur Steigerung der Beratungskompetenz. Mit unserer Expertise erhöhen wir maßgeblich den Absatz renommierter OTC-Produkte und stehen dabei stets im direkten Austausch mit unseren Partnern. Für unser engagiertes Team suchen wir zum nächstmöglichen Zeitpunkt: PTAs als Trainer für Apothekenpersonal in unserem festangestellten Schulungsaußendienst. Wir suchen bundesweit mit den Schwerpunkten auf den Gebieten Frankfurt am Main/Mainz, Karlsruhe, Kassel, Mannheim, München, Nürnberg, Saarbrücken, Stuttgart zum nächstmöglichen Zeitpunkt! Als Apotheken-Trainer gestaltest Du an der Schnittstelle Beratung – Training – Vertrieb aktiv die Pharmawelt von morgen mit und bringst Deine innovativen Ideen ein. Umfassende Betreuung von Top-Apotheken in Deinem Schulungsgebiet Eingehende Schulung des Apothekenpersonals zu den renommierten OTC-Produkten und Arzneimitteln unserer Auftraggeber Gestaltung und Durchführung von Präsentationen sowie Produktschulungen für Apotheken-Teams Unterstützung der Apotheken bei Werbeaktionen und -kampagnen – von der Konzeption bis zur Umsetzung Kundenmanagement vom Erstkontakt bis zur langfristigen Begleitung unserer Partner Abgeschlossene Ausbildung als PTA oder mindestens eine gleichwertige Qualifikation Mindestens zwei Jahre Berufserfahrung im Apothekenumfeld in einer der oben genannten Positionen Kommunikatives, natürliches Auftreten sowie starke vertriebliche Kompetenzen Ausgeprägtes Organisationstalent, Zuverlässigkeit und Flexibilität Umfangreiches Fachwissen über Arzneimittel medizinische Produkte sowie der Wunsch, dieses stetig weiter auszubauen und weiterzugeben Sehr gute rhetorische Fähigkeiten runden Dein Profil ab Abwechslungsreiche Tätigkeiten mit viel Kontakt zu Menschen und der Möglichkeit, Neues zu lernen Intensive Schulungs- und Einarbeitungsphase Mitarbeit bei übergreifenden Projekten zur Weiterentwicklung unseres Angebotsportfolios Attraktives Gehalt sowie Dienstwagen, iPhone und iPad – auch zur privaten Nutzung Einen Zuschuss zur betrieblichen Altersvorsorge
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Senior Scientist (w/m/d) Lyophilized Drug Product Development for Biopharmaceuticals

Do. 02.12.2021
Planegg
Coriolis Pharma is a globally operating independent service provider for formulation research and development of for a large variety of different (bio)pharmaceutical molecules, including proteins, peptides, nucleic acids, ATMPs, GMOs, vaccines and virus(-like) particles. An interdisciplinary team of highly qualified scientists with many years of experience in the development of (bio)pharmaceuticals supported by an expert scientific advisory board provides cutting-edge service and know-how related to the formulation development of biopharmaceuticals. At our company, we pursue one goal every day: the advancement of medicines to cure people. Our expanding company currently employs about 140 people at two sites. Senior Scientist (w/m/d) Lyophilized Drug Product Development for Biopharmaceuticals Contribute scientific expertise Cross functional support for projects teams at Coriolis working on lyophilization projects Provide strategic scientific and technological input into client projects, based on profound experience, best practice and risk mitigation in the field of lyophilization (formulation and process) Give input into experimental planning, support the compilation of workplans and reports Lead, perform and support troubleshooting activities Pass on knowledge to team members and ensure continuous improvement of scientific skills of team members Give internal lectures and trainings at Coriolis Drive implemention of novel technologies and strenghthen scientific expertise in the area of lyophilization Project management Take over the responsibility as project leader, working on client projects with focus on lyophilization of biopharmaceuticals and ATMPs (formulation and lyophilization process development) Project planning, coordination, execution and resource management Ensure that relevant resources are embedded into the project and that project-related decisions are based on state-of-the-art scientific principles University degree in (bio)chemistry, biology, medical sciences pharmacy or related field, PhD beneficial A mininum of 10 years relevant experience Strong scientific background and experience in the field of lyophilization technology Experiences in (bio)pharmaceutical formulation development and characterization Experience in lyophilization under (BL)S2 is of advantage Team player with strong motivation and inter-personal skills Open for new ideas and tasks, can-do attitude and hands on mentality Excellent verbal and written communication skills in English and German  As a Senior Scientist, you will join a highly motivated, interdisciplinary team performing contract research and development for clients from the (bio)pharmaceutical industry worldwide. We offer you diversified and challenging areas of responsibilities in our innovative company. We actively support your personal development (technical, scientific and personal skills) especially by training on relevant techniques for characterization of (bio)pharmaceuticals. Beyond that Coriolis offers a variety of benefits and team activities to its employees.
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