Sie sind hier: Home > Regional > !#platzhalterstadtname!# >

!#platzhalterdienstname!#

Anzeige
Filter

Pharmaindustrie: 31 Jobs in Pfaffenhofen an der Glonn

Berufsfeld
  • Pharmazie 8
  • Teamleitung 6
  • Gruppenleitung 5
  • Leitung 5
  • Abteilungsleitung 3
  • Bereichsleitung 3
  • Außendienst 2
  • Biotechnologie 2
  • Chemie 2
  • Qualitätsmanagement 2
  • Supply-Chain-Management 2
  • Assistenz 1
  • Betriebs- 1
  • Biologie 1
  • Business Intelligence 1
  • Data Warehouse 1
  • Datenbankentwicklung 1
  • Dienstleistung und Fertigung 1
  • Filialleitung 1
  • Forschung 1
Mehr anzeigen
Weniger anzeigen
Branche
  • Pharmaindustrie
Berufserfahrung
  • Mit Berufserfahrung 31
  • Ohne Berufserfahrung 9
  • Mit Personalverantwortung 8
Arbeitszeit
  • Vollzeit 31
Anstellungsart
  • Feste Anstellung 27
  • Befristeter Vertrag 3
  • Arbeitnehmerüberlassung 1
Pharmaindustrie

Clinical Trial Leader (gn)

Mo. 17.05.2021
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: Clinical Trial Leader (gn) Leads the global cross-functional Clinical Trial Team Provides direct operational input into protocol development to ensure efficient and effective delivery of trial objectives Ensures trial operational plans are developed by the vendors with inputs from CTT Develops and executes operational risk management plan highlighting potential risks and actions Creates and drives trial level timelines and deliverables Ensures all trial related documents and systems (e.g. clinical database, IRT and etc.) required for Ethics / Regulatory submissions and trial initiation are developed by the CTT and vendors within the specified timelines Manages and oversees vendor activities and interactions during the conduct of the trial to ensure adherence to the signed contract and agreed timelines and budget Reports and assesses vendor performance ongoing during the trial Collaborates with Clinical Trial Supply Management and vendors to ensure all aspects of the IMP and non-drug supplies (if applicable) are managed throughout the trial Manages and oversees resolution of trial operational issues Collects, tracks, and communicates trial status to the relevant internal / external boards Accountable for accuracy of trial information in all trial databases, trial master file, and tracking systems Manages trial budget, obtains relevant internal board approvals, revises budget when applicable, and reconciles at trial close out Participates in inspection / audit and ensures timely response to inspection / audit observations or other quality issues in cooperation with Quality Assurance Collaborates with CTT to define the scope of responsibilities of operational and medical / clinical data review within the data management plan or equivalent to ensure ongoing quality data review Ideally a minimum of five years operational experience in planning / executing / reporting clinical trials on international level Thorough knowledge of Good Clinical Practice, regulatory processes, and clinical development process Experience with health authority inspections (FDA and/or EMEA) preferred Demonstrated ability to effectively manage trial budget Strong leadership and project management skills in a cross functional and multicultural team Excellent in negotiation and conflict resolution Fluent English (oral and written) 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
Zum Stellenangebot

Clinical Operational Manager (gn)

Mo. 17.05.2021
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: Clinical Operational Manager (gn) Being a core member of Clinical Trial Team (CTT) including deputizing the CTL during his/her absence in leading the CTT Organize CTT meetings including agenda preparation, actions tracking and follow-up Collect and track trial status such as enrollment and timelines to monitor the trial progress and to update the relevant internal / external boards (e.g. Global Program Team) Prepare trial outsourcing specifications with input from the CTT, and coordinate the vendor selection process including business process walkthrough together with the Category Manager In collaboration with other CTT functions, set-up and maintain trial-related processes/systems and their key performance indicators (e.g. central laboratories, interactive response technologies (IRT), Clinical Trial Management Systems (CTMS), data analytics tools, clinical supplies) with the vendors as per protocol requirements and internal standards Oversee the interfaces between the trial vendors and the established processes / systems to ensure accurate data or information flow including data integration, data transfer and reconciliation of information at the agreed time intervals Access and address vendor performance during the trial conduct and escalate (if required) to the Clinical Trial Team for further actions Develop the ethics submission plan in collaboration with the Clinical Trial Leader, Clinical Trial Manager, Regulatory Affairs Manager and the CRO for implementation in the participating countries and clinical sites to obtain approvals to conduct the trial Monitor the progress of the status of the ethics submissions and approvals, and intervene as required to resolve the issue with the CRO Take the role of a CTL as assigned in clinical trial and lead the cross-functional CTT to operationalize the protocol Ensure inspection / audit readiness including TMF documentation and participates in internal audits and inspections as required Bachelor’s or Master’s Degree / PhD or equivalent qualification in life science / healthcare Ideally a minimum of five years clinical research experience, previous involvement with clinical trial development, implementation or reporting activities preferred Knowledge of Good Clinical Practice and experience with the end to end clinical trial process including the interfaces Strong leadership with ability to lead a cross functional team in a matrix environment and to demonstrate collaboration skills Excellent interpersonal, communication, organization and coordination skills and ability to influence without authority Ability to resolve issues independently and understand when to escalate Fluent English (oral and written) 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
Zum Stellenangebot

Scientific Reviewer (m/w/d)

Sa. 15.05.2021
Planegg
Coriolis Pharma, is a globally operating independent service provider for formulation research and development of (bio)pharmaceuticals (proteins, peptides, monoclonal antibodies, nucleic acids, vaccines, etc.). 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 (bio)pharmaceuticals. Provide scientific and technological support for Coriolis’ project teams in biopharmaceutical formulation development and/or analytical characterization projects: Assist project managers during detailed experimental planning and troubleshooting Review of Coriolis’ documents in client projects Conduct literature studies Discussion and alignment of data and results in the overall scope/context of the study Write executive summaries/project summaries Take part in meetings and telephone conferences with clients Support business development in the scientific assessment of new project requests and the definition of the project strategy Support Coriolis’ management in scientific questions and strategy Involvement in training and continuing education of Coriolis’ employees   Representation of Coriolis at conferences Scientific support of internal research projects at Coriolis PhD degree in pharmacy, pharmaceutical sciences, biochemistry, biophysics, or related field 10+ years experience in formulation development and drug product development for biopharmaceuticals (protein therapeutics, ATMPs and/or vaccines) In-depth scientific know-how in the field of formulation development and analytical characterization of biopharmaceuticals Lyophilization expertise and regulatory experience are beneficial for the position Team player with a high intrinsic motivation and enthusiasm for science and innovation Excellent communication skills (in English) Excellent scientific writing skills As a Scientific Reviewer, you will join a highly motivated, interdisciplinary team performing contract research and development for clients from the (bio)pharmaceutical industry worldwide. In this cross-functional position you will support Coriolis’ project teams by providing scientific and technological guidance for drug product development projects, with focus on formulation development (liquid and lyophilized) and analytical characterization for biopharmaceuticals, including vaccines and advanced therapy medicinal products (ATMPs). We offer you diversified and challenging areas of responsibilities in our innovative company. We actively support your personal development and the realization of your own ideas, i.e.g., specialization on management or scientific tasks. As a Scientific Reviewer there is the flexibility to work from remote and/or on-site at Coriolis.
Zum Stellenangebot

Digital marketing Manager, EU & US Drug Discovery Services (m/w/d)

Sa. 15.05.2021
Planegg, 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. Inbound & outbound marketing campaigns for Drug Discovery Services Develop, measure and optimize Proteros’ Digital Marketing Programs using Social Media Ad platforms (including Linked-In), Google Adwords, Google tools and HubSpot Website analytics, (SEO), optimization and maintenance CRM: create new leads and expand outreach by marketing and research measures Develop, measure and optimize Proteros’ marketing & communication strategy and campaign management Develop and optimize outbound marketing collaterals and activities Solid inbound/outbound marketing experience in life-sciences for Europe and US In-depth experience in digital marketing campaigns and paid advertisement (Linked-In, Twitter, Facebook,…) Proficiency in marketing and automation and blogging software e.g. Hubspot Enhanced website maintenance and optimization skills Proven strong lead-generation skills and track-record, extended CRM communication and analysis skills Strong communicator and team-player with business acumen Commercial experience in Life Science Industry (preferable CRO / Drug Discovery) in an matrix organization Scientific background: ideally Master in Biology, Life Sciences or equivalent Bonus skills: HTML / CSS, Adobe Creative Suite A superb, jump-start from a brand-new marketing conception and close interaction with outstanding marketing agency An inspiring creative, flexible, agile and passionate working atmosphere A multicultural, interdisciplinary teams and an open corporate culture Market competitive salary and benefits Position based in the biotech hub of Martinsried near Munich
Zum Stellenangebot

Senior Manager (gn) Regulatory Affairs

Sa. 15.05.2021
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: Senior Manager (gn) Regulatory Affairs Global Regulatory Affairs is actively involved in the development and life-cycle management of medicinal products thereby contributing to appropriateness of the drug development path as well as to compliance with applicable pharmaceutical legislation / regulation.The purpose of the regulatory affairs senior manager is to provide support and or manage in the preparation and execution of global regulatory strategies and to manage the submission, approval, and maintenance of applications for clinical trials, marketing applications or other related regulatory submissions. Manage the regulatory submission process through to approval including management and coordination of the preparation of all regulatory documentations at different Regulatory milestones Manage the regulatory agency interactions, document preparation, co-ordination rehearsals and minutes Contribute to development and evaluation of regulatory strategies for projects Review and provide regulatory comments to quality, safety and efficacy or labeling related documents (e.g. protocols, reports) to be included in a regulatory submission (e.g. Clinical Trial Applications, IND, Scientific Advice, HA interactions, Answers to Authorities, orphan designation, annual report, pediatric pans, ODD, DSUR, PIP etc.) Contribute to the development of risk assessment pertaining to the quality, safety and efficacy documentation / data of investigational medicinal products related applications Professional skills & experience Minimum of five to seven years’ industry experience of which at least four years’ regulatory experience Experience in preparation and submission of a full submission / or large variation / supplement in at least one ICH region through to authorization Experience in all phases of drug development Experience with regulatory agency interactions and preparation of documentation to support interactions Experience in IND / CTA requirements Knowledge of international regulatory affairs Experience with maintenance of regulatory authorizations Experience with supporting a project with development activities eCTD experience Personal skills & competencies Excellent written and spoken communication skills Good interpersonal skills Attention to details Ability to work in teams Awareness of Regulatory Affairs Contribution to Pharma business Good organizational and planning skills 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
Zum Stellenangebot

Tax Assistant (gn)

Fr. 14.05.2021
Planegg
MorphoSys hat sich der Entwicklung heraus­ragender und inno­vativer bio­pharma­zeutischer Medi­kamente ver­schrieben, um so das Leben schwer­kranker Patienten zu ver­bessern. Hierbei sind innovative Techno­logien und intelligente Ent­wicklungs­strategien von zentraler Bedeutung. Unser Erfolg basiert auf unseren Mit­arbeitern. Bei allem was wir tun, streben wir Spitzen­leis­tungen an und arbeiten eng über Fach­bereiche hinweg zusammen. Vertrauen und Respekt im Umgang mit­einander prägen unsere Zusammen­arbeit. Unser aller Anspruch ist es, die Medikamente von morgen zu entwickeln. Freuen Sie sich auf ein Umfeld, in dem jeder seine Talente ent­falten kann. Kommen Sie zu uns nach Planegg bei München! Wir haben zum nächstmöglichen Zeitpunkt folgende Position zu besetzen: Tax Assistant (gn) Koordination der Berechnung von tatsächlichen und latenten Steuern in Jahres- und Quartals­abschlüssen nach IFRS und HGB Erstellung der Steuererklärungen und Prüfung von Steuerbescheiden Unterstützung und Beratung von Konzerngesellschaften in steuerlichen Fragestellungen, insbesondere Transfer Pricing Sicherstellung und ständige Verbesserung der Tax Compliance und SOX-Prozesse Begleitung von Betriebsprüfungen Mitarbeit an steuerlichen Sonderprojekten Abgeschlossene kaufmännische Ausbildung und Weiterbildung zum Bilanzbuchhalter (gn) oder ein erfolgreich abgeschlossenes Studium der Wirtschaftswissenschaften mit den Schwerpunkten Rechnungswesen, Steuern und/oder Finanzen Gute steuerliche Kenntnisse (Ertragsteuern, Umsatzsteuer, Quellensteuer, latente Steuern, Transfer Pricing, Tax Compliance) Ausgeprägtes Verständnis von Buchhaltungs-/ Steuerprozessen Gute Kenntnisse der Rechnungslegung nach IFRS und HGB Praktische Erfahrung in der Steuerberatung oder in der Steuerabteilung eines Unternehmens Erfahrung mit ERP-Software (idealerweise SAP Business by Design) DATEV-Kenntnisse Kreatives Arbeiten in X-functional Teams Offene und wertschätzende Unternehmenskultur Multikulturelles Umfeld Arbeiten in einem attraktiven, hochwertig ausgestatteten Gebäude mit Betriebsrestaurant Kostenfreie Sportangebote und Sprachkurse
Zum Stellenangebot

Leiter (m/w/d) Gesamt-IT

Fr. 14.05.2021
Planegg
Coriolis Pharma zählt weltweit zu den führenden unabhängigen Dienstleistungsunternehmen für die Formulierungsforschung und -entwicklung von (bio-) pharmazeutischen Arzneimitteln und Impfstoffen. Bei Coriolis Pharma verfolgen wir täglich ein Ziel: die Weiterentwicklung von Medikamenten zur Heilung von Menschen. Unser expandierendes Unternehmen beschäftigt derzeit circa 130 Mitarbeiter an zwei Standorten. Leiter Gesamt-IT (m/w/d)Ohne IT läuft fast nichts bei uns. Die Coriolis IT ist mehr als eine interne Supporteinheit.Zusammen mit Ihrem agilen Team stellen Sie als Leiter Gesamt IT unserem Unternehmen innerhalb einer virtualisierten Umgebung alle Corporate-IT-Services zur Verfügung, vom IT-Support, einer integrierten IT-Entwicklung, bis zum Betrieb der Infrastruktur mit allen relevanten Netzwerkkomponenten. Umsetzung der unternehmensweiten strategischen Weiterentwicklung der IT-Organisation orientiert an der digitalen Transformation Bündelung der einzelnen IT Units: Data Science Application, Strategic IT Projects, Core IT Opera­tions, User Support und GMP IT zu einer Gesamt-IT Unit Unterstützung der stetigen Optimierung unserer Geschäftsprozesse und Richtlinien und Entwicklung dazu passender IT-Umsetzungskonzepte Ausbau der digitalen Unternehmens-IT-Architektur durch die Verzahnung technischer, orga­nisatorischer und prozessualer Aspekte Leitung und Entwicklung eines hochmotivierten wachsenden Teams von aktuell 7 Mitar­beitenden Sicherstellung der zielgerichteten Nutzung neuer Technologien und Collaboration-Tools, z.B. zur Prozessoptimierung und digitalen Automatisierung entsprechend des Unter­nehmens­bedarfs Erweiterung des Informationssicherheitsstandards von Coriolis verzahnt mit dem Daten­schutz und anderen gesetzlichen Vorgaben und Anforderungen Übernahme des IT-Programm-Managements aller relevanten IT-Projekte vom Design, über das Qualitätsmanagement, bis hin zum Deployment neuer IT-Services und Funktion als Ansprechpartner für interne Stakeholder und externe IT-Dienstleister   Abgeschlossenes Studium der Informatik, E-Technik/ Informationstechnik, Wirtschafts­wissenschaften oder einer vergleichbaren Studienrichtung mit langjähriger Berufs­erfahrung Tiefgreifendes Wissen über Entwicklungen, Tools und Best Practices digitaler Trans­formation, idealerweise im Life Science-, bzw. Pharma- Umfeld Einschlägige Erfahrung als Führungskraft / Entscheidungsträger, sowie weitreichende Erfahrung als Projektmanager. Praxiserprobtes Verständnis betriebswissenschaftlicher Prozesse und deren Übersetzung in innovative, high end IT Lösungen Strategisch-konzeptionelle Vorgehensweise, hohes Umsetzungsvermögen, sowie unternehmerische Persönlichkeit mit der Fähigkeit, neue Produkte, Services und Geschäfts­modelle zu etablieren Hohe Lösungsorientiertheit mit Change-Erfahrung Sehr gute Kommunikations- und Präsentationsfähigkeiten in deutscher und englischer Sprache auf allen Ebenen des Unternehmens Versierter Umgang mit den neuesten Tools und Technologien und hohe Affinität für neue Trends und Entwicklung von cutting Edge IT-Lösungen Als stark wachsendes Unternehmen bieten wir Ihnen die Möglichkeit als erfahrener Leiter IT (m/w/d) abwechslungsreiche vielfältige Aufgaben und Verantwortung zu übernehmen und unsere wachsende IT-Organisation maßgeblich zu gestalten und weiterzuentwickeln. In einem internationalen Team ermöglichen wir Ihnen kompetenzbasierte Entwicklungsmöglichkeiten. Neben einer leistungsgerechten Vergütung und zahlreichen Benefits, bieten wir außerdem einen attraktiven Arbeitsplatz am Standort Martinsried im südlichen Teil von München.
Zum Stellenangebot

Scientist Downstream Processing (gn) Antigens

Mi. 12.05.2021
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: Scientist Downstream Processing gn* The scientist will be part of the downstream processing team with the following responsibilities: Work on cutting-edge technologies with the aim of generating differentiated, more efficacious and safer engineered antibody-based therapeutics for patients Design synthetic expression constructs; use your deep understanding of protein structure and function to create novel protein constructs, focus is on the generation of antigens Purify, and characterize proteins from mammalian or bacterial cells by different chromatographic techniques Perform method development, technology evaluations and implement new technologies Supervise technical assistants and coordinate project tasks with other scientists to ensure efficient, high-quality antigen production Present and discuss results within MorphoSys cross-functional project teams and with external partners PhD in the field of life sciences or equivalent degree in biotechnology, biology, cell biology, biochemistry or related disciplines preferably complemented by post-doc or industry experience Hands-on experience in purification technologies using state-of-the-art chromatography systems as well as in the production and analysis of proteins Experienced in engineering and modeling complex protein molecules with potential biotechnological and biomedical applications Teamplayer with well-developed communication skills Ability to coordinate and manage parallel project streams Systematic, careful and responsible execution of experiments Excellent oral and written communication skills in English and German 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
Zum Stellenangebot

Head of External Supplier Operations (gn)

Mi. 12.05.2021
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: Head of External Supplier Operations (gn) Act as a point of contact for business collaborations with Contract Manufacturing Organizations (CMOs) ensuring that the overall relationship is healthy Implement harmonized governance structures across all vendor accounts Establish harmonized procedures i) across different suppliers, ii) across multiple projects, iii) across all stakeholders / internal departments Coordinate and contribute to contract establishment and vendor selection procedures by leading negotiation and selection teams. Set-up contractual standards in close collaboration with the internal Business and Quality units Continuously monitor key procedures via uniform performance indicators and stakeholder reviews and ensure compliance with contractual terms Responsible for performance monitoring and reporting and ensure compliance with contractual terms Collaborate with the internal Technical Project Leaders, Supply Chain, QA and Regulatory functions to drive continuous improvement of the overall business relationship with CMOs Collaborate with the Finance Business Partner on regular budget monitoring and control, system improvement and harmonization Optimize business interactions with key suppliers in order to continuously improve quality, efficiency and innovation Bachelors or Master's Degree in Engineering, Biotechnology or related field Ideally more than eight 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
Zum Stellenangebot

Group Leader (w/m/d) Drug Product Development for Biopharmaceuticals

Mi. 12.05.2021
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 (bio)pharmaceuticals. For our headquarters in Munich - Martinsried, we are looking for a highly motivated and dedicated Group Leader (w/m/d) Drug Product Development for Biopharmaceuticals Lead a group of 8 – 12 direct reports, i.e., scientists with academic degree, working on client projects with focus on liquid formulation development and characterization of biopharmaceuticals and vaccines Ensure operational success of the group and associated team members Responsible for the successful execution of client projects within the group Responsible for the development of team members, i.e., creating a strategy for building up the group on a qualitative as well as quantitative level Responsible for performance appraisals and career development of the team members Work cooperatively alongside colleagues and key stakeholders across teams (e.g., Business Development, Contract Management, etc.) Maintain cutting edge scientific knowledge in biopharmaceutical formulation development and characterization technology Support the implemention of innovation and continuous improvement of the organization Responsible to ensure quality related regulations are implemented and followed in the group Master or equivalent, University degree in (bio)chemistry, biology, medical sciences pharmacy or related field, PhD beneficial 6+ years experience and in-depth knowledge in drug product development and regulatory requirements of biopharmaceuticals and/or vaccines Track record in leading teams in an interdisciplinary and international environment Leading by example, open for new ideas and tasks, can-do attitudes and hands on mentality Significant experiences as project manager with strong project management skills such as resource management, delegation and controlling, prioritization, risk management and coordination of mutidisciplinary project teams Team player with strong motivation and inter-personal skills Excellent verbal and written communication skills in English and German As a Group Leader, 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. The well-being and health of our employees is very important to us. Even in this current situation, we have a distinctive hygiene concept in addition to workplace health programs, which we consistently implement and further develop during the application process, as well as during onboarding and daily work.
Zum Stellenangebot
1234


shopping-portal