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Weitere: Naturwissenschaften und Forschung: 15 Jobs in Bergkirchen

Berufsfeld
  • Weitere: Naturwissenschaften und Forschung
Branche
  • Pharmaindustrie 5
  • Sonstige Dienstleistungen 3
  • Wissenschaft & Forschung 3
  • Bildung & Training 2
  • Konsumgüter/Gebrauchsgüter 1
  • Medizintechnik 1
  • Nahrungs- & Genussmittel 1
  • Sonstige Branchen 1
Berufserfahrung
  • Mit Berufserfahrung 15
  • Ohne Berufserfahrung 4
  • Mit Personalverantwortung 2
Arbeitszeit
  • Vollzeit 15
  • Home Office 1
  • Teilzeit 1
Anstellungsart
  • Feste Anstellung 13
  • Befristeter Vertrag 2
Weitere: Naturwissenschaften und Forschung

Leiter Betrieb Collaboration (w/m/d)

Fr. 22.01.2021
München
Seit 1866 gilt unsere Leidenschaft der Technik und der Sicherheit. Innovationen beeinflussen unser Leben in vielfältiger Weise. Für die Sicherheit von Menschen und der Gesellschaft setzen wir uns jeden Tag aufs Neue ein und schaffen Vertrauen in neue Technologien. Wir sind Teil des Fortschritts. Wir beraten, wir prüfen, wir zertifizieren. Wir handeln aus Überzeugung, gestalten schon heute die Welt von morgen – setzen Zeichen. Wir nehmen die Zukunft in die Hand. Wir sind TÜV SÜD – 25.000 Mitarbeiter an weltweit 1.000 Standorten. Die TÜV SÜD Business Services GmbH ist der interne Dienstleister für in- und ausländische Gesellschaften des TÜV SÜD Konzerns. Durch hochwertige und skalierbare Dienstleistungen in den Servicelines Einkauf, Facility Management, IT, Personal und Rechnungswesen wird das Wachstum der TÜV SÜD Unternehmensgruppe unterstützt. Wenn Sie die Zukunft mit uns gestalten wollen, freuen wir uns auf Ihre Bewerbung. Personalverantwortung sowie Ergebnisverantwortung für die Fachabteilung Betrieb Collaboration Verantwortung für den Betrieb und die Weiterentwicklung der Kommunikationsplattform rund um Microsoft Office 365 (Exchange, Yammer, Teams etc.) Sicherstellung des gesamtheitlichen Supports von Microsoft Office 365 Abgeschlossene Ausbildung im naturwissenschaftlichen Bereich Erfahrungen im Bereich Projektmanagement Sehr gute Kenntnisse in ITIL sowie in Microsoft Office 365 und seinen Komponenten Routinierter Umgang mit den MS Office-Anwendungen Sensibilität im Umgang mit Kunden und Mitarbeitern Innovationsfähigkeit und -bereitschaft Ausgezeichnete analytische Fähigkeiten Teamfähigkeit und hohe soziale Kompetenz Verantwortungs- und Kostenbewusstsein Selbstständigkeit, Einsatzbereitschaft und ausgeprägte Delegationsbereitschaft Fähigkeit zur Konsensbildung und Konfliktbewältigung Sichere Englischkenntnisse in Wort und Schrift Der besseren Verständlichkeit halber verwenden wir durchgängig – grammatikalisch – männliche Bezeichnungen, adressieren dabei aber Personen aller Geschlechter gleichermaßen. Themen wie die berufliche Gleichstellung aller Menschen haben bei TÜV SÜD einen hohen Stellenwert.
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International Regulatory Affairs Liaison Lead (m/f/x)

Fr. 22.01.2021
München
Daiichi Sankyo and its 15.000 employees in more than 20 countries are dedicated to the creation and supply of innovative pharmaceutical products. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology. Our European headquarters are in Munich, Germany and we have affiliates in 13 European countries including Denmark, where Copenhagen acts as the Nordic headquarter. For our headquarters in Munich we are seeking highly qualified candidates to fill the position International Regulatory Affairs Liaison Lead (m/f/x) To provide International Regulatory Strategy support for projects, products and non-project work. Act as a single point of contact for Tier 2 and 3 country regulatory submissions, accountable overall for filing strategies and marketing application reviews in these regions. Represent International Regulatory Affairs internally working on a collaborative basis with Global Regulatory Leads to become a fully recognised member of a multi-disciplinary global project team, providing expertise on international regulatory matters. Role and Responsibilities: Advise and support Local/regional regulatory teams for assessing regulatory landscape and regulations to optimise our regulatory strategies and submission plans within and across the product portfolio and provide actionable Regulatory Input into Development Strategy to enable timely commercial desirable registrations across the regions. Advise global teams on any specific local requirements or gaps in the global clinical development to support local submissions and collaborate to develop mitigation plans (e.g. bridging/sub-population requirements). Champion for countries to obtain the needed global and regional resources (e.g. to participate in global registration-directed trials, to prepare bridging reports, to respond to health authority queries rapidly). Interface between Global and Local Regulatory Teams and communicate project specific information to local teams, ensuring alignment between registration/submission requirements and local development plans, translate global regulatory expectations into local plans and lead the execution of these plans. Strategise with Global Regulatory Lead (GRL) and other core Global Regulatory Team (GRT) members on the regulatory strategy for NCEs and major variations (e.g. line extensions, new indications, label enhancements). Co-lead with Global Regulatory Leads (GRLs) development and execution of the Global Regulatory Engagement Plan. Participate in external partnership negotiations, execution and implementations, when applicable, to ensure advanced awareness of regulatory risks and seamless integration. Represent Global Regulatory Affairs on International product issues, and on specific non-product related projects. Participate or lead assigned non-project tasks and process improvements pertinent to International Regulatory Affairs. Keep current with, review and interpret international regulatory and scientific regulations and initiatives, communicate important changes and trends with the relevant stakeholders, making recommendations to senior management. 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 10 years of experience in the pharmaceutical industry Minimum of 8 years of experience in global regulatory affairs with emphasis on International drug development and marketing authorisation applications in LATAM, Eastern European Region, Middle East as well as other International Markets. Experienced people leader. Experience of working in global environment. Proven ability to plan, coordinate and lead submission activities simultaneously. Excellent personal and intercultural skills paired with the ability to work cross functionally in a multinational organisation. Ability to develop and maintain good relationships, gain the trust of others, challenge views and 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, Spanish and/or French as a second language preferred. 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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Team Lead (w/m/d) Klinische Studien Monitoring & Recruiting

Fr. 22.01.2021
Gräfelfing
FUTRUE ist ein international tätiger Healthcare Incubator, der mit mehr als 20 Unter­nehmen und mehr als 70 Arzneimittel­zulassungen u.a. in den Bereichen intelli­gente Bakterien, inno­vative Schmerz­therapien, chemiefreie Arznei­mittel, medizi­nisches Cannabis und Orphan Diseases tätig ist. Unser Fokus liegt dabei auf der Identi­fikation von inno­vativen und bereits weit ent­wickelten Wirk­stoffen mittels unserer weltweit tätigen Scouts. Nach einem Status­check der präklinischen und klinischen Daten anhand eines eigens ent­wickelten Algorithmus startet ein hoch standardi­sierter Prozess, um alle aus­stehenden Daten für eine zeitnahe Zulassung zu generieren. Eigene speziali­sierte Marketing- und Sales-Teams stellen die Information der Fach­kreise und damit eine zeitnahe Patienten­versorgung mit dem jeweiligen Arznei­mittel sicher. Unser Anspruch liegt darin, schneller zu sein als jede andere Pharma­firma – denn unsere Patienten haben keine Zeit! Dabei setzen wir auf eine neue Generation dynamischer Talente, die den Mut hat, unge­wohnte Wege zu gehen.Für unser Team Klinische Studien suchen wir der­zeit einen Leiter (w/m/d) für das Moni­toring und das Patienten- bzw. Ärzte-Recruiting. Mit Deinem Team verantwortest Du das gesamte Patienten- / Ärzte-Recrui­ting und steuerst unsere externen Dienstleister. Du erarbeitest Recruiting-Stra­tegien für die Gewinnung von Patienten und Ärzten für unsere klinischen Studien und dis­kutierst diese auf Management-Ebene. Du bist für die Initiierung von Studien­zentren verantwortlich und erster Ansprech­partner (w/m/d) für unsere Prüfärzte. Zudem bist Du für das gesamte Monitoring unserer klinischen Studien verantwort­lich, unter der Berück­sichtigung fristgerechter Erstellung von qualitativ hoch­wertigen Berichten und Follow-Up-Briefen der Monitoring-Besuche. Du verfügst über ein erfolgreich abgeschlossenes naturwissenschaftliches Studium (z.B. Ernährungs­wissenschaften, Biologie oder Biochemie) und mehrjährige Berufs­erfahrung, idealer­weise im Projektmanagement von klinischen Studien. Neben einer hohen Sorg­falt bringst Du die Bereitschaft zum termin­gerechten Arbeiten mit. Du bist ein Teamplayer (w/m/d) und kannst Dich schnell sowie eigen­ständig in wechselnde Themen­gebiete einarbeiten. Du verfügst über hervor­ragende ICH-GCP-Kenntnisse zur ordnungs­gemäßen Durch­führung von klinischen Studien. Dich zeichnen eine verantwortungs­bewusste Arbeitsweise und Organisations­stärke aus. Du sprichst hervor­ragend Deutsch und Englisch und verfügst außerdem über fundierte MS-Office-Kennt­nisse sowie einen Pkw-Führerschein. Wir bieten Dir einen vielfältigen, anspruchs­vollen Job mit spannenden Aufgaben und einem breiten Spektrum an Gestaltungs­möglichkeiten! Wir bieten ein innovatives Umfeld zur beruflichen Entfaltung mit kurzen Entscheidungs­wegen und dem Frei­raum, auch einmal neue Wege zu gehen! Außerdem warten auf Dich: Flache Hierar­chien und eine offene Kommunikation – nur so kannst Du Dich weiter­entwickeln und dazu bei­tragen, dass unsere Produkte von unserem gegen­seitigen Austausch leben. Verantwortung – nach einer Einarbeitungs­phase durch einen erfahrenen Kollegen oder Dein Team Lead bekommst Du die Gelegen­heit, Deinen eigenen Bereich zu betreuen. Hast Du das Entrepreneur­ship in Dir? Dann schaffen wir gemeinsam Großes! Frische Vitamine – wöchent­lich wirst Du mit unserem Obstkorb versorgt, der Dir die nötige Energie verleiht. Firmenfeiern sind für uns selbst­verständlich – ob Sommer­fest, der traditionelle Wiesn-Besuch oder die all­jährliche Weihnachtsfeier. Eine Dachterrasse mit Alpen­panorama – entspanne Dich während der Mittags­pause und tanke Sonnen­strahlen bei gutem Wetter.
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Supplier Relationship Manager (gn)

Fr. 22.01.2021
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! As part of the CMC organization, the Supplier Relationship Manager will coordinate the implementation of harmonized collaboration models, ensure efficient interactions with Contract Manufacturing Organizations (CMOs), and leverage Operational Excellence tools to continuously accelerate business performance of MorphoSys’ growing supplier network. We would like to fill the following vacancy as soon as possible: Supplier Relationship Manager (gn) Act as a point of contact for business collaborations with CMOs, ensuring that the overall relationship is healthy Optimize business interactions with key suppliers in order to continuously improve quality, efficiency and innovation in respective processes with the suppliers Establish harmonized processes i) across different suppliers, ii) across multiple projects, iii) across all stakeholders / internal departments Support and coordinate the implementation of harmonized governance structures across all vendor accounts, organize governance meetings and follow up with internal and external stakeholders Collaborate with the Finance Business Partner on regular budget monitoring and controlling, system improvement and harmonization Coordinate and contribute to contract establishment and vendor selection procedures. Responsible to set-up contractual standards in close collaboration with the internal Business and Quality units  Continuous monitoring of key processes via uniform performance indicators and stakeholder reviews and ensuring compliance with contractual terms Collaborate with the Technical Project Leader and Supply Chain functions to drive continuous improvement of the overall business relationship with CMOs; establish and execute operational excellence and LEAN approaches to drive continuous efficency gains in supplier interactions Bachelors or Master's Degree in Engineering, Biotechnology or related field Ideally more than eight years years of relevant experience in the pharmaceutical, biopharmaceutical or related industry     Understanding of GMP principles and regulatory requirements in pharmaceutical development Knowledge of suppliers, industry trends and emerging players in global pharmaceutical manufacturing services Knowledge of, and previous experience with supplier management procedures in a pharma / biotech environment Good organizational awareness of relevant business units within a global supplier network Demonstrated experience in negotiating supply and manufacturing agreements with external suppliers Demonstrated knowledge of tools and techniques of Operational Excellence / Lean methods Ability to work efficiently across culturally diverse global matrix organizations Excellent project management skills to efficiently coordinate, prioritize and manage multi-parallel tasks and objectives Highly motivated and open-minded team player with well-developed interpersonal abilities Excellent oral and written communication skills (German would be a plus) Effective presentation, negotiation and conflict resolution skills Proficiency with MS Word, Excel and PowerPoint required 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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Clinical Evaluation Specialist (w/m/d)

Mi. 20.01.2021
München
Wir gehören zu den weltweit führenden Unternehmen im Bereich Orthopädie, Arthroskopie, Sportmedizin und Orthobiologie. Getreu unserer Mission Helping Surgeons Treat Their Patients Better entwickeln wir seit über 35 Jahren innovative Produkte und Operationsverfahren. Arthrex wurde 1981 in München gegründet - heute befindet sich unser Hauptsitz in Naples (Florida, USA) mit weiteren Niederlassungen in 21 Ländern. Unsere Firmenkultur ist geprägt von einer länderübergreifenden Zusammenarbeit sowie einem Austausch mit Kolleginnen und Kollegen unterschiedlicher Nationalitäten. Die Erschließung neuer Geschäftsfelder und die Erweiterung unserer Produktpalette tragen zu einem stetigen Wachstum bei und lassen uns auch in Zukunft federführend bei der Entwicklung qualitativ hochwertiger Produkte sein. Unsere Mitarbeiterinnen und Mitarbeiter tragen mit ihrem Engagement wesentlich zu diesem Erfolg bei. Dafür bieten wir ein motivierendes, wertschätzendes Arbeitsumfeld. Zur Unterstützung der Abteilung Orthopedic Research suchen wir ab sofort in München einen Clinical Evaluation Specialist (w/m/d) Sie führen umfangreiche Literaturrecherchen im Bereich der Orthopädie und Sportmedizin durch Sie identifizieren literaturbasierte Evidenz für klinische Akzeptanzkriterien Sie arbeiten eng mit der regulatorischen Abteilung bei der Beantwortung klinischer Fragestellungen zusammen Sie erstellen und aktualisieren die klinischen Abschnitte von Clinical Evaluation Reports gemäß MEDDEV 2.7/1 Sie unterstützen die Ausarbeitung von Studienprotokollen Sie analysieren und interpretieren klinische Daten und fassen diese in Form von Präsentationen und wissenschaftlichen Texten zusammen Sie stimmen sich regelmäßig mit globalen Mitgliedern aus den Bereichen Forschung, Produktmanagement, Regulatory u.a. ab Sie haben Ihr Studium im Bereich Naturwissenschaften, Mediziningenieurwesen, Life Science, etc. erfolgreich abgeschlossen oder verfügen über eine vergleichbare Qualifikation Sie bringen mehrjährige Erfahrung im wissenschaftlichen Arbeiten mit Mit den gängigen MS-Office-Programmen sind Sie bestens vertraut und haben bereits mit Statistiksoftwares wie SPSS oder JMP gearbeitet Sie haben bereits Erfahrung mit einschlägigen Gesetzen und Standards im Medizinproduktesektor (MDR, MDD, ISO 14155), mit der Erstellung klinischer Bewertungen gemäß MEDDEV 2.7/1 sowie mit Literaturrecherchen und -datenbanken (Pubmed, Embase, etc.) Sie sind motiviert, arbeiten sehr zuverlässig sowie selbstständig und übernehmen gerne Verantwortung Eine gute und vertrauensvolle Zusammenarbeit im Team ist Ihnen genauso wichtig wie uns Fließende Englisch- und sehr gute Deutschkenntnisse in Wort und Schrift runden Ihr Profil ab Eine Tätigkeit in einem internationalen Umfeld Persönliches und wertschätzendes Miteinander Ein zukunftssicherer Arbeitsplatz Flexible Arbeitszeiten und in vielen Bereichen die Möglichkeit zur mobilen Arbeit Individuelle Einarbeitung, ergänzt durch umfangreiche Einführungsschulungen Betriebliche Altersvorsorge (im unbefristeten Beschäftigungsverhältnis) Kostenlose Krankenzusatzversicherung Unterstützung in verschiedenen Lebenslagen (z.B. Kinderbetreuung, Pflege, persönlichen Fragestellungen, etc.) durch eine Kooperation mit einem Dienstleister Von Montag bis Donnerstag kostenloses Mittagessen
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Head of Quality Assurance (m/w/d)

Mi. 20.01.2021
Planegg
Coriolis Pharma, is a globally operating independent service provider for formulation research and development of (bio)pharmaceutical drugs (proteins, peptides, monoclonal antibodies, RNA/DNA, etc.) and vaccines. 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.As Head of Quality Assurance (m/w/d) you are responsible for the continuous improvement of quality management systems at Coriolis. Your main tasks will be: Organization of a Coriolis wide quality management system including disciplinary responsibility for the Coriolis quality assurance unit Heading of the GMP QA group and coordination of GRP (Good Research Practice) QM team Planning and performance of internal audits for all quality relevant units Planning, implementation and follow-up of corrective actions resulting from audits and authority inspections Compilation and approval of a yearly QM status report for senior management Organization of QM systems for deviations, CAPAs, changes, OOS and complaints according to GMP/GRP regulations Securing that QM systems such as equipment qualification programs, supplier qualification and/or method validation programs are in place Organization and management of a system for employee training according to GMP/GRP regulations Establishment of a good relationship to regulatory authorities and clients, coordination and follow-up of authority inspections and client audits. Negotiation, approval and implementation of Quality Assurance Agreements in quality related matters Securing the compliance according to client quality arrangements together with relevant internal stake holders (e.g., Head QC, group leaders, project managers) Conduction of risk analysis, deviation investigations and changes for QA related topics Close collaboration with BD, IT, HR GMP-QC and all operational units with respect to QM related matter Approval of GMP-CoA/CoTs Master or equivalent University degree in (bio) chemistry, biology, medical sciences or pharmacy, PhD preferred Excellent knowledge of GMP and relevant regulations (AMG; AMWHV, Pharm. Eur. USP, JP, ICH, GAMP) At least 5 years professional experience and track record in GxP environment of pharmaceutical or biotech companies Excellent written and verbal knowledge of English and German   Very good MS Office skills (Excel, Word, Outlook) Very good organizational skills and assertiveness Very good communication and leadership skills Exact and structured way of working Experience in leading people As a fast-growing company, we offer you the opportunity to take on the exciting tasks and responsibilities as Head of Quality Assurance for our GMP/GRP units. We invite you to design and establish processes and structures and continuously improve our existing QM systems. In an international team, we provide you with competence-based development opportunities. In addition to performance-related remuneration and numerous benefits, we also offer an attractive workplace at the location of Martinsried. You are reliable, show commitment, want to apply knowledge and learn new things, carry out projects, ensure quality, make a team contribution and work sustainably as well as develop solutions? Then we look forward to receiving your application, including your salary requirements and earliest possible starting date.
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Science Manager (m/f/d) at the MDSI (Munich Data Science Institute), ELLIS Munich

Di. 19.01.2021
Garching bei München
The Munich Data Science Institute is an integrative research center at the Technical University of Munich (TUM) that carries out research, teaching and promotion of young talents with an interdisciplinary and cross-faculty focus on the field of data science and in particular machine learning. Recently ELLIS Munich, the Munich unit of the European Lab for Learning and Intelligent Systems (ELLIS), has been set up and we are looking for an engaged dynamic personality to join our team having as main focus of activity the coordination and implementation of ELLIS activities at our Institute. The contract will be initially limited to two years. Management, coordination and implementation of different activities around further set-up and extension of the ELLIS Unit Munich Providing strategic and operational structure for ELLIS activities at TUM, such as meetings of the steering and management board. Organisation and implementation of various scientific activities and events (exchange and visiting programs, network meetings, etc.) Contribution to third-party funding proposals and reporting, including the ELLIS network and the MDSI as a whole Fostering the interaction and collaboration with further ELLIS stakeholders such as the Helmholtz Center Munich and other Universities, coordinating communication and joint initiatives Support of activities related to the Munich Center for Machine Learning and other MDSI related activities A Master University degree in engineering, natural- or computer science or mathematics. A PhD is desirable Experience in science management in an university or research institution is highly welcome A reliable, collaborative, creative and with own initiative approach to work Strong analytical and critical thinking skills and the ability to manage a broad range of tasks and responsibilities Strong written, verbal communication and presentation skills in both English and German with high level of comfort communicating effectively across internal and external organizations and across hierarchies Very good user knowledge of MS-Office applications; experience with project management software and CMS are desirable Full responsibility from the start in an innovative environment and with real impact at the forefront of science and technology Opportunity to advance the data science and machine learning ecosystem at TUM and in Munich and extend the international network of collaborations in these fields Highly dynamic and networked working environment with inspiring talents and leaders, renowned experts and researchers The position is initially limited to two years. Employment and remuneration is in accordance to TV-L 13. Place of employment is Garching bei München. Applications from disabled persons with essentially the same qualifications will be given preference. TUM strives to raise the proportion of women in its workforce and explicitly encourages applications from qualified women.
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Conformity Assessment Procedure Specialist – IVDR (f/m/d)

Di. 19.01.2021
München
At TÜV SÜD we are passionate about technology. Innovations impact our daily lives in countless ways, and we are dedicated to being a part of that progress. We test, we audit, we inspect, we advise. We never stop challenging ourselves for the safety of society and its people. We breathe technology, we strive for professional excellence, and we leave a mark. We take the future into our hands. We are TÜV SÜD – more than 25,000 highly skilled employees across 1,000 offices worldwide. If you would like to shape the future with us, we look forward to receiving your application.The candidate will be responsible to assure that all processes implemented in Product Service Division by corresponding process owners are in line with the regulatory requirements of the IVDR: Overall responsibility for up to date compliance to the assigned conformity assessment scheme and applicable standards Creates awareness for the essentials of the conformity assessment scheme and related changes Identifies regulatory risks and reviews changes in processes and QM documents for regulatory compliance Supports process owners, certification bodies and project leaders (e.g. for digitization projects) to find the most efficient and effective solutions in compliance with the requirements of the conformity assessment scheme and applicable standards Performs spot checks and internal audits of the conformity assessment scheme Analyses quality problems for risks of non-compliance to regulatory requirements Trains on overall conformity assessment scheme and how individual processes relate to the scheme University Degree in field of engineering, biology, chemistry, or related discipline Five years of professional experience in regulatory affairs or related field Sound knowledge with medical device regulatory requirements e.g. IVDD/IVDR, MDR and ISO 13485 Demonstrated experience in project management Strong team related thinking Fluent commad of English and German language (written and spoken)
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Associate Principal Scientist in MEU Meals Brand Value (m/w/d)

Mo. 18.01.2021
München
At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about. We have a rich portfolio of strong brands – both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum. Our 80,000 Makers and Bakers are located in our operations in more than 80 countries and are working to sell our products in over 150 countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast. Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Working as part of a cross-functional team, you are recognized internally as a technical expert in an area of importance to the RDQ function. You identify, define and solve complex business problems by applying your broad and in-depth technical knowledge. As an expert in your technical specialty, this technical leadership role requires you to interact with senior management and cross-functional teams to meet current and future strategic demands of the business.Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Working as part of a cross-functional team, you are recognized internally as a technical expert in an area of importance to the RDQ function. You identify, define and solve complex business problems by applying your broad and in-depth technical knowledge. As an expert in your technical specialty, this technical leadership role requires you to interact with senior management and cross-functional teams to meet current and future strategic demands of the business. What you will bring A desire to drive your future and accelerate your career and the following experience and knowledge: Using your excellent technical expertise to set and deliver the RDQ agenda Effectively influencing category leads (e.g. vice presidents) Using critical thinking and thought leadership to ensure that solutions are developed for complex issues Working collaboratively in a fast-paced commercial and technical environment Coaching and mentoring others Expertise in Cream Cheese technology and Process cheese technology. Filling the long term productivity funnel in MEU BV. Leading QI activities to grow the core in cream cheese.Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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Associate Scientist II (m/w/d)

Mo. 18.01.2021
München
At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about. We have a rich portfolio of strong brands – both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum. Our 80,000 Makers and Bakers are located in our operations in more than 80 countries and are working to sell our products in over 150 countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast. Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Working as part of a cross functional team, you deliver the RDQ activities required to complete new product development, portfolio maintenance and/or productivity projects with an emphasis on meeting the desired consumer experience.How you will contribute With the support and guidance of a manager, you will organize and execute projects in line with RDQ, marketing and manufacturing requirements, effectively communicating status and risks. You will plan and conduct pilot plant and factory trials in accordance with good manufacturing practice and HACCP requirements and development activities (e.g. product shelf-life testing, designing for quality, consumer test preparation etc.). You will also write technical reports that will require the analysis and interpretation of results and that lead to conclusions and recommendations and create and maintain accurate consumer-led specifications. What you will bring A desire to drive your future and accelerate your career and the following experience and knowledge: Food science, science, or engineering ideally in a fast-moving consumer goods market Working on teams and independently with the guidance of a manager Prioritizing and managing activities Identifying problems proactively and creating and implementing solutions independently Applying fundamental technical understanding to interpret and analyze data to reach clear conclusions Communicating effectively verbally and in writing, including technical writing Putting the consumer at the heart of development activities More about this role: Scientist supporting product development from concept through prototyping and scale up Carrying out pilot and plant trials including product testing Carrying out shelf life testing Writing product specifications Welche Zusatzqualifikationen du mitbringst: Science/engineering background in food technology Good English skills, other language skills very welcome Proficient computer skills, MS office, internet Team oriented mind set Independent working style/self starter/problem solving skills Reisetätigkeit: 30-50%Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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