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Vifor Pharma

Die Vifor Pharma Gruppe – die frühere Galenica Gruppe – ist ein globales Spezialitäten-Pharmaunternehmen, das eigene Pharmaprodukte erforscht, entwickelt, herstellt und vertreibt und ein bevorzugter Partner für innovative patientenorientierte Lösungen ist.
Das Unternehmen hat sich zum Ziel gesetzt, ein globaler Marktführer in den Bereichen Eisenmangel, Nephrologie und kardiorenale Therapien zu sein und weltweit Patienten mit schweren und chronischen Erkrankungen zu einem besseren Leben in Gesundheit zu verhelfen.
Die Vifor Pharma Gruppe verfügt über Produktionsstätten in der Schweiz und in Portugal sowie über ein dynamisches Netzwerk von Vertriebsgesellschaften und Partnern zur weltweiten Marktabdeckung. Das Unternehmen treibt die Expansion seiner weltweiten Präsenz laufend voran, bleibt dabei aber in seinem schweizerischen Heimmarkt fest verwurzelt.
Die Vifor Pharma Gruppe besteht aus Vifor Pharma, Vifor Fresenius Medical Care Renal Pharma, ihrem gemeinsamen Unternehmen mit Fresenius Medical Care, Relypsa und OM Pharma.

Vifor Pharma

Flughofstrasse 61
8152Glattbrugg

02.08.2020

Vifor Pharma

Procurement Lead R & D - Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 02.08.2020

  • Vollzeitstelle

For Global Procurement, we are looking for a Procurement Lead with focus on R&D and sub-categories. The main goal for this position is to, in collaboration with the global R&D organization, create and drive a business focused procurement strategy as well as performing sourcing activities and implement procurement innovation across the Group. The person we are looking for is a passionate procurement professional, with a genuine R&D understanding in order to collaborate with the R&D organization in the optimal way. The position reports into the Head of Global Procurement and will be part of the procurement leadership team. The successful candidate will join Global Procurement, a passionate team of procurement professionals from across the globe, and the main tasks would be: Developing category strategies in close collaboration with key stakeholders Coordinating multi-unit, cross-functional global projects and supporting of local, regional and global implantations Leading and managing competitive bids, contract negotiations and contracting Manage suppliers within the R&D category, through a standardized Supplier Relationship Management process Identification and implementation of savings opportunities by applying best practices Bring procurement innovation into processes and supplier management Furthermore, your profile meets the following criteria: You hold a Bachelor- or Master degree in business, economics or R&D related fields You bring minimum 3 years’ experience within procurement, consulting, key account management or research & development Experience in negotiation & contracting You have strong project management skills, you are able to deal with complex initiatives and to lead through persuasion with all levels of the company as well as across different cultures Excellent verbal written communication skills in English. Additional languages are a big plus Experience in dealing with R&D business stakeholders and suppliers in a procurement environment would be considered an advantage Solid financial acumen and strong analytical skills. SAP knowledge and experience is a plus Open for international business travel as per business needs (approx. 10%) We offer the successful candidate a challenging position in a strong and world leading pharma company in which you will find and environment with room to maneuver. As we are in the process of establishing Global Procurement team, the candidate will be able to influence the final role setup largely.
Inserat ansehen

30.07.2020

Vifor Pharma

Clinical Development Director Cardiorenal - Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 30.07.2020

  • Vollzeitstelle

Due to its expanding portfolio, Vifor Pharma has an excellent opportunity for a Clinical Development Director for our cardiorenal therapy area. This role will be a part of our global clinical development team based in Glattbrugg, Zurich. Reporting to the Clinical Development Lead for Cardiorenal, the Clinical Research Director will be responsible for medical and scientific contribution to protocols, new product and indication opportunities, drug safety, study reports, IBs, regulatory submissions, manuscripts, medical education, and other projects requiring medical/scientific research, analysis, evaluation, training and reporting. Key responsibilities (but not limited to): Leadership of clinical study/program to ensure delivery of clinical trials per ICH-GCP requirements and meeting timelines and budget Leadership and moderation of clinical advisory boards and ongoing interactions with applicable committees relevant to successful conduct of studies and programs In collaboration with a cross-functional team, drive the development of effective and innovative clinical trial designs, and facilitate execution of clinical trials by supporting site and CRO personnel, safety monitoring activities, data clean-up activities, data analyses, and clinical study report development and finalization Author protocols, and provide scientific input into manuscripts/publications, IBs, regulatory and study reports Research and analyse scientific/medical information and data with respect to clinical trials, safety databases, and other medical/scientific elements necessary for decision-making and regulatory submissions Assess safety data including labs and SAEs on an ongoing basis for ongoing clinical trials; manage DSMB processes for clinical trials Represent the company as the scientific subject matter expert at external meetings including those with Investigators, Steering Committees, Key Opinion Leaders and Advisory Groups Provide Medical Oversight and Medical Monitoring to interventional clinical trials (supported by CROs, if applicable) Maintain and evaluate current knowledge of key disease areas, providing information to appropriate groups as needed Evaluate investigator-initiated protocols and make recommendations (if applicable) Requirements: Educational background: MD (strongly preferred) or internationally recognized equivalent degree or PhD in science/health-related discipline 6 to 8 years of pharmaceutical industry experience gained in clinical research Experience in phase 3 and 4 clinical studies/outcomes trials is an advantage Knowledge and experience of clinical trial design, data analysis, statistics and research methods Knowledge of the drug development process and clinical research methodologies Trained in GCP regulations, and familiar with ICH and FDA guidelines relevant to clinical development Experience in Cardiology and/or Nephrology clinical trials would be preferrable Experience in writing and submission of Health Authority documents (e.g., NDA, sNDA, MAA) desired Ability to work independently and in a fast paced, hands-on, flexible, dynamically changing environment If this opportunity is of interest to you, please apply by submitting your updated CV via our careers website.
Inserat ansehen

23.07.2020

Vifor Pharma

Director Global Business Development – Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 23.07.2020

  • Vollzeitstelle

We are looking for a Director Global Business Development to join the Business Development and Licensing Team (BD&L) at our operational headquarters in Glattbrugg, Zurich. As an expert in finance and business modelling with emphasis on development stage life sciences companies, products and services you will report to the Head of BD&L and be responsible for, but not limited to, the following: Seek out and generate data required to build robust BD&L business cases (financial models) that are aligned with insights generated during the due diligence process Manage research including external consultants or service providers (recruitment, briefing, definition of deliverables, etc.) Collaborate closely with stakeholders and data providers of adjacent departments, namely Market Analytics, Medical Affairs, Regulatory, Market Access and Clinical Development Create, own and present content for investment opportunities to the Executive Committee. Support the development of BD&L updates to the Board of Directors of Vifor Pharma Be the “project owner” in regards to BD&L opportunities assigned to you and ensure the transition of those business cases to Corporate Finance and the implementation of operational activities in Project Management once a deal is closed Support efforts to identify new companies, new products and services and ultimately new investment ideas that are in alignment with the strategic needs of the Vifor Pharma Group Create your own network of internal and external partners Be part of a BD&L department and participate with team members in the early evaluation and project triage of newly identified opportunities (deal flow) You bring strong analytical and conceptual skills. You enjoy creating your own models in Excel and expressing your findings by creating a convincing storyline. Specifically, we are looking for a person with the following profile: University degree in Biology/Chemistry/Medicine or equivalent natural or medical sciences higher education Further business and administration education (e.g. MBA) and/or Financial Analysis (e.g. CFA) is an important additional asset 7-10 years of professional experience in a Pharma BD&L function or relevant corporate positions within the Life Sciences Industry (Business Development/Venture Capital/Private Equity/Investment Banking) Firm understanding of the general drug discovery, development and commercialization process is a requirement Previous exposure to nephrology or heart failure is considered an additional asset Help in the advancement of the team, the development of new skills and the continuous improvement of quality Excellent oral and written communication skills in English and German Good story-telling capabilities Entrepreneurial spirit and can-do attitude You are self-motivated, proactive, and have a result-driven personality and are ready to step into action when required. You have an open and communicative personality, which fits well with your ability to work in interdisciplinary teams. You have high client orientation and a passion for close collaboration with a wide range of stakeholders. Your ability to deliver high quality work under time pressure reflects your interest in working in a dynamic and international work environment such as Vifor Pharma.
Inserat ansehen

25.06.2020

Vifor Pharma

Regulatory Affairs Partner Business Manager – Japan expert – Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 25.06.2020

  • Vollzeitstelle

We are currently looking for a Regulatory Affairs Partner Business Manager to join our Regulatory Affairs team. In this role you will be our Japan Regulatory Expert and also deal with other Key Asian Markets (eg China, South Korea, and other Asian Markets) This role reports directly to the Head Regulatory Affairs Business Partner and is planned to be based in Zurich. Your responsibilities will include: Acts as Single Point of Contact between Regulatory Affairs of the partner company, local regulatory representatives of Vifor Pharma and corporate or regional stakeholders Manages successfully assigned regulatory projects Maintains the assigned Regulatory Data Base Entries in TrackWise according to internal guidelines Organizes and supports Regional Regulatory Meetings with the partner companies Has oversight on all regulatory actions in the area of responsibility Clarifies requirements for planned regulatory activities Represents GRA International at in-house meetings, e.g. Demand Review Meeting Manages the response to Health Authority questions / requests for information Systematically identify and eliminate insufficiencies/discrepancies in the approved regulatory documentation Support GMP inspections of manufacturing sites by competent authorities Supplies Regional Hub / partner companies with required regulatory documents Improves internal regulatory work flows and processes Ensures compliance of regulatory dossiers with legal requirements in close collaboration with other functions of Global Regulatory Affairs such as the Therapeutic Groups, Labelling, RegOps and CMC Keeps up to date with the latest regulatory requirements with the focus on the key market Japan. Further tasks according to directives from Line Manager The successful candidate is willing to work effectively with a wide variety of personnel across diverse teams and functions internally as well as external partners. In addition, you will bring the following profile: Degree in Life Sciences 4 to 6 years of experience in Regulatory Affairs, preferably in Japan or in any other APAC country Good command of English and Japanese Leadership and cross-cultural competences Strategic thinking, analytical and result-oriented mindset Ability to analyze the regulatory requirements, perform comprehensive gap assessments and build effective regulatory strategies Project and matrix team management capabilities (direct/indirect people management experience is an advantage) Computer literacy: advanced skills in Word, Excel and PowerPoint This position demands excellent communication and negotiation skills at all levels, and discretion in the handling of confidential information You describe yourself as a good communicator, with strong teamwork skills as well as good organization and negotiation abilities. You demonstrate accuracy and attention to details with a focus on quality and regulatory requirements. Finally, you are able to cope with stress and demonstrate discretion in the handling of confidential information
Inserat ansehen

10.08.2020

Vifor Pharma

Head Process Engineering & Validation - Geneva

  • Vifor Pharma

  • Switzerland - Meyrin/Geneva

  • 10.08.2020

  • Vollzeitstelle

To strengthen the growth of OM Pharma, we are currently looking for a Head Process Engineering & Validation for our manufacturing plant in Geneva. In this function, you report to the Head of Product and Industrial Development (P&ID). You will manage and share responsibilities with a team of two Validation Engineers. At this position, you will successfully establish and implement validation strategies as well as lead Process Engineering activities by ensuring compliance according to standards and international guidelines, assessing Validation gaps and delivering projects in due time. These activities will cover both Biotechnology and Pharmaceutical processes. Your main missions are: In the frame of Technical Projects, products LCM and compliance activities, ensure that all validation activities i.e. Manufacturing, Cleaning Processes & Transport Validation comply with GMP regulations in force Establish and implement validation strategies, lead their execution in close collaboration with Manufacturing, QA, QC and P&ID teams: validations, continued process verification, periodic revalidations Lead and bring new expertise for process engineering activities to improve process capability, quality and compliance: process mapping, identification of process improvement Implement Continued Process Verification (CPV): monitoring and data analysis of process parameters by applying a statistical approach Team management: supervise staff, develop the team & people, ensure reliability, meet deadlines, make decision in a timely manner, promote team cohesion and ownership, ensure operational effectiveness Review and approve protocol and reports generated by the team, manage deviations, CAPA, change control, SOPs related to the activity Act as Project Manager or Team Member for technical projects of the site: lead process engineering, validation for biotech & pharmaceutical manufacturing and cleaning processes Contribute to prepare and review documents in support of CMC regulatory filings and addressing queries from HA’s related to validations Act as a key interface with HA’s regarding validation topics (Q&A and inspections) For this role, we are a looking for a strong technical and strategic leader, bringing the following profile: PhD, Master, Engineer’s Degree in pharmaceutical sciences 10 years experience in validation in biotech pharmaceutical industry in GMP environment Extensive experience on Process engineering, Process Capability Management and Statistical analysis Proven experience in Team Management Cross functional skills (Manufacturing, QC, RA, QM) Previous experience in Project Management Fluent in French and English both in oral and written conversation. To be successful in this new created role, we are looking for an experienced leader with capability to coach team members and flexibility to adapt to changes. You describe yourself as solution oriented, flexible and have an organized approach . Thanks to your communication skills, you easily develop new relationships and feel comfortable in a situation where you need to influence and convince others, internal and external stakeholders . Furthermore, your strategic thinking enable you to examine and understand issues from multiple points of view and your scientific analytical skills help you to identify challenges and hurdles.
Inserat ansehen

03.08.2020

Vifor Pharma

Regulatory Affairs Teamlead - Geneva

  • Vifor Pharma

  • Switzerland - Meyrin/Geneva

  • 03.08.2020

  • Vollzeitstelle

We are currently looking for an experienced Regulatory Affairs Team Lead who will lead key activities for EU, US and CH regions. You will be responsible for the definition and implementation of regulatory strategies based on the good knowledge and appropriate interpretation of guidelines and directives. Based in Geneva, you will report to the Head of Regulatory Affairs OM Pharma and your responsibilities will include: Contribute to the definition and the implementation of regulatory strategies to expand the business (geographic expansion, new indications…) and support/maintain registrations Coordinate life cycle activities / maintenance of existing product licenses Coordinate dossiers submission according to the defined timelines (renewals, variations, responses to HA questions) Ensure compliance of the portfolio with legal requirements Conduct risk assessments and set-up mitigation plans Cooperate with internal stakeholders to ensure alignment on strategies Lead the EU, US and CH regions team (2 direct reports): be responsible for the management and development of staff by overseeing recruitment and training, evaluating performance, defining and assigning responsibilities, providing opportunities for career development We are looking for a customer- and service-oriented person who brings experience in working with a wide variety of stakeholders across diverse teams both internally and with external partner companies. Furthermore, your profile meets the following criteria : University Degree (PhD / MSc) in Life Sciences, Pharmaceutical Sciences or Medical 10 years of experience in Regulatory Affairs, with a proven experience on US market (new registrations) and EU region (support to clinical trials activities) Experience in people management and development Ability to perform comprehensive gap assessments and build effective regulatory strategies (Good knowledge and appropriate interpretation of guidelines, directives etc…) Self-assertion, creative and solution-oriented work approach Strategic thinking and acting, entrepreneurship skills Excellent communication and negotiation skills at all levels, diplomacy and respectful behavior Good command of French and English both in oral and written conversation You are a mature regulatory professional and describe yourself as a solution-oriented and flexible person, able to influence internal and external stakeholders. Your work is characterized by its accuracy, a proactive approach and you are able to work under pressure and to deal with tight deadlines. These skills will ensure your success in this role.
Inserat ansehen

09.08.2020

Vifor Pharma

Manager Strategic Supply Chain Projects / NPIs - St. Gallen / Zurich

  • Vifor Pharma

  • Switzerland - St Gallen

  • 09.08.2020

  • Vollzeitstelle

We are currently looking for a Manager Strategic Supply Chain Projects / NPIs to join our Supply Chain team located in St. Gallen and Zurich. In this global role, reporting to the Head NPIs & Strategic Partnerships, you will manage and be a key contributor to strategic cross-functional projects and new product introductions (NPIs), from a global supply chain perspective. Your tasks will include: Project management of end-to-end supply chain setup for new products: Lead cross-functionally to ensure optimal supply chain setup and ensure timely alignment with operational teams Manage seamless transition of new products and launch activities to routine commercial operations in full cooperation with involved functions Establish and maintain excellent and authoritative relations with global stakeholders such as business partners, customers, logistics providers and act as ambassador for Global Supply Chain Design, establish and optimize the complete supply chain for products in focus of this role, to the best interests of the business and our patients, and in alignment with internal and external partners Secure, analyze and monitor initial demand plans for the NPIs, identify deviations to plan and lead mitigation activities in cooperation with Customer Operations and Planning teams Ensure an optimal TTM (time to market) and flawless launch execution from a supply chain perspective Drive close alignment with commercial operations regarding supply / commercial strategy for the product(s) Compile and synthesize supply chain relevant data such as in-market sales, stock levels, etc. to support supply chain objectives and ensure continuous product availability Represent and drive supply chain interests at various cross-functional strategic meetings, including presentation work The successful candidate needs to have excellent communication skills and the ability to work successfully across different sites, functions and management levels, and will bring the following profile: University Degree in International Management or Supply Chain Management Minimum 5 years of experience in a relevant Supply Chain Function (e.g. Procurement, Planning, Customer Service, Demand Management) Minimum 3 years of experience in the Pharmaceutical Industry; other relevant experience in a highly regulated industry may be considered Proven project management skills Fluent in English (written and verbally), German is an advantage Additional preferred requirements: Proficiency in use of ERP systems and MS Office products (Excel, Project, ThinkCell, PowerPoint) GMP / GDP experience You describe yourself as a strong customer- and service-oriented personality. You show a high level of flexibility, work effectively in a cross-functional and cross-regional environment and are able to adapt to the ever changing business environment. We are looking for someone who is a role model for others in terms of the Vifor Pharma Values and continuously displays a positive can-do attitude. Finally, your proven experience in a similar position will allow you to be successful in this position and in line with Vifor Pharma values.
Inserat ansehen

09.08.2020

Vifor Pharma

Lehrstelle Chemie- und Pharmatechnologe EFZ 2021 – St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 09.08.2020

  • Vollzeitstelle

Für unseren Standort in St. Gallen suchen wir eine/n Lernende/n Chemie- und Pharmatechnologin / Pharmatechnologe. Die unter der früheren Berufsbezeichnung Chemikant / Chemikantin Chemie- und Pharmatechnologen bekannten Fachleute sind Produktionsspezialisten in der pharmazeutischen und chemischen Industrie. Bei Vifor Pharma bedienen sie computergesteuerte Anlagen zur Herstellung von hochwertigen pharmazeutischen Wirkstoffen, die in anderen Betrieben zu Medikamenten weiterverarbeitet werden. Sauberkeit und Ordnung sind im pharmazeutischen Betrieb ebenso essentiell wie eine exakte Dokumentation. Diese Aufgaben setzen voraus, dass Chemie- und Pharmatechnologen alle Anlagen in ihrem Arbeitsbereich genau kennen, ein gutes technisches Verständnis haben und über Grundkenntnisse in Technologie, Chemie und Physik verfügen. Die Kenntnisse, welche zum Erfüllen der Stelle erforderlich sind, werden während der 3-jährigen Ausbildung erlangt. Zu Antritt der Ausbildung sind folgende Qualifikationen erforderlich: Abschluss Sekundarschule Interesse an Technik Kenntnisse in Naturwissenschaften (Chemie, Physik und Mathematik) Konzentrationsfähigkeit Gute Deutschkenntnisse in Wort und Schrift Zuverlässigkeit und ausgeprägtes Verantwortungsbewusstsein Gute körperliche Konstitution Kommunikations- und Teamfähigkeit Flexibilität Sie ergänzen unser Team optimal, wenn Sie über eine exakte und eigenverantwortliche Arbeitsweise verfügen. Wir freuen uns auf eine Person mit Interesse an der pharmazeutischen Industrie, welche unser Team künftig tatkräftig unterstützen möchte.
Inserat ansehen

05.08.2020

Vifor Pharma

Administrator/in Stabilität 40% - Befristet auf 2 Jahre - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 05.08.2020

  • Vollzeitstelle

In dieser Funktion arbeiten Sie in einem kleinen Team an unserem modernen Produktionsstandort in St. Gallen. Sie sind verantwortlich für die Überwachung von extern durchgeführten Stabilitätsstudien, wobei Sie nach Bedarf auch die Stabilitätsprüfung vor Ort unterstützen. Ziel von Stabilitätsstudien ist es herauszufinden, wie sich ein pharmazeutisches Produkt oder Wirkstoff während der Lagerung bei bestimmten klimatischen Bedingungen über die Zeit verändert. Aus den Ergebnissen werden u.a. die Haltbarkeit und empfohlenen Lagerbindungen abgeleitet. Dabei erfüllen Sie folgende Aufgaben: Kontrolle der externen Stabilitätsstudien und -resultate Kommunikation mit externen Dienstleistern/Partnern (Agenda-, Pendenz- und Mailbox-Verwaltung) Erstellung und Durchsicht von Plänen und Berichten zu Stabilitätsstudien Datenbereitstellung für die jährlichen Stability Quality Reviews für jedes unserer Produkte Mithilfe beim Transfer analytischer Methoden zu unseren externen Dienstleistern/Partnern Um diese Aufgaben erfolgreich zu meistern, bringen Sie nebst einer zuverlässigen und sorgfältigen Arbeitsweise folgende Kompetenzen mit: Abgeschlossene technisch-naturwissenschaftliche Ausbildung oder Bachelor-Studium Sicherer Umgang mit MS-Office Sehr gute Deutsch-Kenntnisse Gute Englisch-Kenntnisse Interesse an der Qualitätskontrolle von Arzneimitteln und Arbeit im GMP-gerechten Umfeld Sie erkennen und überprüfen gerne Aufgaben Dritter und führen dafür das notwendige Mass an Kontrolle selbständig durch. Zudem sind Sie eine interessierte und flexible Persönlichkeit, die sich rasch auf neue Fragestellung einstellt und Teamarbeit schätzt.
Inserat ansehen

28.07.2020

Vifor Pharma

Lehrstelle als Laborant/in EFZ Fachrichtung Chemie 2021 - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 28.07.2020

  • Vollzeitstelle

Deine Aufgaben Für diese anspruchsvolle Berufslehre als Laborant/in EFZ suchen wir Sekundarschul-Abgänger oder Personen mit adäquater Ausbildung und starken Leistungen in Mathematik. Während deiner Lehrzeit lernst du folgende Tätigkeiten kennen: Praktische Durchführung wissenschaftlicher Untersuchungen Synthese und Analyse von chemischen Substanzen Berechnen und Durchführen von chemischen Reaktionen Wägen, Messen und Bestimmen von Substanzen, Gasen und Flüssigkeiten Erfassen und Interpretieren von Daten Die Berufsschule wirst du in St. Gallen besuchen. Die ersten zwei Jahre an 2 Tagen die Woche und im letzten Jahr an 1 Tag die Woche. Wenn du die BMS abschliessen möchtest, findet der Unterricht durchgehend 2 Tage die Woche statt. Dein Profil Du besuchst die Sekundarschule und verfügst über gute schulische Leistungen. Mathematik und naturwissenschaftliche Fächer gehören zu deinen Stärken und du hast Freude an chemischen und technischen Vorgängen. Zudem kannst du dich mit folgendem Profil identifizieren: Logisch-abstraktes Denkvermögen und rasche Auffassungsgabe Ausgeprägte Konzentrationsfähigkeit, Geduld und Ausdauer Freude am Experimentieren und Beobachten Exakte und systematische Arbeitsweise Gute Team- und Kommunikationsfähigkeit Wir wünschen uns eine/n Kandidaten/in welche/r gerne in einem international tätigen Pharmaunternehmen das Laborteam ergänzen möchte. Du bist motiviert Neues zu lernen und kannst dich für technische Herausforderungen begeistern.
Inserat ansehen

22.07.2020

Vifor Pharma

IT Business Analyst / Application Specialist – St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 22.07.2020

  • Vollzeitstelle

We are seeking an IT Business Analyst / Application Specialist who will be based at Vifor (International) AG in St. Gallen and will ensure that the main applications TrackWise and Oracle AGILE within the area of responsibility are available, stable and secure. In this role, the person will report to the to the Head of Business IT Applications and will be part of the Global IT. The person will be responsible for the following tasks: Ensure the availability of the applications and their services (Trackwise, Oracle Agile and Medgate) Support on the 2nd and coordinate the 3rd level application support Ensure that all services delivered are optimal and cost effective Ensure the availability of further small applications and their services Manage on-going maintenance of systems and documentation Support IT policies, practices and standards (e.g. IT Security Manual) Address privacy and security gaps and risks Coordination and technical lead of IT projects, creation of IT concepts for this area Risk analysis and implementation of changes and bug fixes The ideal candidate is an Information Technology professional and brings the following skills and experience: Minimum 5 years of experience in IT role, preferably as Business Analyst or Application Specialist/ Application Manager Minimum 3 years project management experience Experience in pharmaceutical or chemical industry In depth knowledge of Sparta - TrackWise Good knowledge in Oracle AGILE as well as OpenText – LiveLink / Content Server Knowledge and understanding of basic IT-Systems (Windows, Oracle, etc.) Capability to understand business needs, requirements and relationships Fluency in English both verbally and in written, German language is an advantage Good incident managing skills (e.g. working with ticket system and external partners) Knowledge in IT Service Management and ITIL Knowledge of GAMP and GxP guidelines For this role, we are looking for a proactive candidate who demonstrates entrepreneurial approach and can drive the necessary activities to bring our infrastructure and services to the next level. Being in that role will allow to underline the necessary «can do» attitude, team player spirit and act as a role model for others in line with Vifor Pharma values.
Inserat ansehen

11.07.2020

Vifor Pharma

Global Records Manager - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 11.07.2020

  • Vollzeitstelle

We are seeking a Global Records Manager who will be based at Vifor (International) AG in St. Gallen and who will coordinate the Data Classification and Records Management (DCRM) project, support the Global Document Management and the quality applications LIMS and TrackWise. In this role, the person will report to the Head Global Digital Quality Systems and will be part of the Technical Operations team. The person will be responsible for the following tasks: Coordinate the Project DCRM (Data Classification and Records Management) in cooperation with the Project Leader Steer and lead the DCRM activities as Global Records Manager Provide administrative and user support including training of key users for the Global Digital Quality Systems Support the implementation and roll-out of additional process workflows on global as well as on-site level Provide 1st level support and handle related incidents in the ticketing tool SNOW Support the development, validation, implementation and maintenance including validation on Vifor sites level Help ensuring a compliant validation status and inspection readiness Support maintenance, building up and actualization of documents such as, handbooks, SOPs, templates etc. for the use of Digital Quality Systems and training of its users Support the creation of reports and queries (e.g. SQL or Jasper reports in LIMS) Manage the follow-up of activities resulting from periodical key user meetings The ideal candidate brings the following essentials skills and experience: Minimum 3 years of work experience in a similar role, preferably in the Pharmaceutical, Chemical and/or Medical Device industry Experience in project management and coordination of project activities Experience with document/records management including classification of data and related E2E processes Knowledge in GxP and/or Medical Device requirements Work experience with validation of computer systems Fluency in English and German (written and spoken) Good knowledge of Microsoft Office Applications (e.g. Word, Excel, PowerPoint, Visio) The following skills would be advantageous: Demonstrated ability to successfully collaborate across different sites, functions, management levels and cultures Experience with computer systems and the business administration role, especially in the area of Quality Management Additional languages would be advantageous For this role, we are looking for a proactive candidate who demonstrates entrepreneurial approach and can drive the necessary activities to bring our infrastructure and services to the next level. Being in that role will allow to underline the necessary «can do» attitude, team player spirit and act as a role model for others in line with Vifor Pharma values.
Inserat ansehen

09.08.2020

Vifor Pharma

Head of Communications Switzerland – Fribourg

  • Vifor Pharma

  • Switzerland - Villars-sur-Glâne/Fribourg

  • 09.08.2020

  • Vollzeitstelle

Our successful Swiss Affiliate is looking for a Head of Communications Switzerland, who will report directly to the General Manager and dotted line to the Global Head of Corporate Communications. In this role, you will work closely with the Headquarter as well as with the local Swiss sites and are in charge of the communication of Vifor Pharma in Switzerland. You goal is to ensure positive presence and reputation of the company within local trade media. Your main responsibilities include: Strengthen position of Vifor Pharma Switzerland as a patient-centric organisation in the Swiss market Ensure consistency and alignment of Corporate Communications activities and local Business strategy Manage local media relations strategy with trade magazines and ensure execution Act as local spokesperson and as responsible person for local Crisis Communications Develop and implement local employee engagement activities including town halls and events, employee-relevant stories and articles, including publishing on intranet Draft Swiss statements, Q&As, press materials and write, edit and approve content Be responsible for local change and business transformation communications Anticipate reputation or business issues and prepare for mitigations Develop media plan with Swiss marketing and medical teams ensuring consistent messaging from corporate with local disease awareness & education and local product brand communications Contribute to corporate digital communications For this role, we are looking for a passionate, pragmatic and creative person, bringing the following profile: University degree in Journalism, Communications or similar At least 8 years’ experience in professional communications in a Corporate or Agency environment Experience in the pharmaceutical industry is strongly preferred Profound experience in internal and external communications, strategy development, digital, crisis management, product & change communications Good knowledge of the Swiss media landscape and social media analytics Expertise in managing multiple projects at the same time Experience in working and advising senior management and executives German as mother tongue, with very good command both in oral and written conversation in French and English You demonstrate a strong customer orientation and feel comfortable in a position, where you make decisions and take initiatives to move things forward. You are an innovative, determined and assertive person, who is able to work efficiently on his own as well as in cross-functional teams. Your negotiation ability, analytical skills and strategic thinking enable you to achieve performance and to federate others towards your ideas.
Inserat ansehen

07.08.2020

Vifor Pharma

IT Business Analyst / Application Specialist (Serialization) - Fribourg

  • Vifor Pharma

  • Switzerland - Villars-sur-Glâne/Fribourg

  • 07.08.2020

  • Vollzeitstelle

We are looking for an IT Business Analyst / Application Specialist to join our Business Applications team at our Swiss affiliate in Fribourg, Villars-sur-Glâne. You will report to the Group Leader Business Applications and your responsibilities will include, but not be limited to: You will be responsible for the serialization tool and application provider management process in line with existing internal/external regulations and policies Develop and maintain the serialization application life cycle management roadmap in line with the IT and application management strategy Drive continuous improvement of the serialization applications to meet and sustain compliance with internal and external regulatory requirements in alignment with local/global QA Ensure that the serialization system is meeting regulatory requirements for serialization and track & trace Ensure serialization system availability and support according to internal/external Service Level Agreements (SLAs) and Operations Level Agreements (OLAs) Ensure compliance of serialization applications & interfaces Partner with business in the definition, assessment and implementation of serialization requirements Furthermore, your profile meets the following criteria: Bachelor’s degree in Engineering, Supply Chain & Logistics, IT or directly related field Minimum 3 years of experience in application management in the pharmaceutical industry with knowledge of pharmaceutical regulatory guidelines for computer system validation (CSV, GAMP, FDA 21 CFR Part 11, PIC, etc.) or equivalent qualification from another regulated industry (e.g. banking) Experience as an application expert or partial project manager throughout the project lifecycle in the area of supply chain management, logistics or production Sound technical understanding of relevant application including configuration, customization, administration, interfaces, etc. Proficiency in use of MS Office products (Excel, PowerPoint, Access) Fluency in English and either German or French language (good command of both, written and spoken language is mandatory) For this role, we are looking for a proactive candidate who demonstrates entrepreneurial approach and can drive the necessary activities to bring our infrastructure and services to the next level. Being in that role will allow to underline the necessary «can do» attitude, team player spirit and act as a role model for others in line with Vifor Pharma values.
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02.08.2020

Vifor Pharma

Head of Human Resources Swiss Affiliate - Fribourg

  • Vifor Pharma

  • Switzerland - Villars-sur-Glâne/Fribourg

  • 02.08.2020

  • Vollzeitstelle

We are currently recruiting for an accomplished Head of Human Resources, taking a unique opportunity to overlook our Swiss affiliate. As a Head of Human Resources, you will act as a local HR Partner for the Swiss Commercial Entity, providing expert guidance on all HR matters, as well as strategic operational input to truly make things happen. Based in Fribourg (Villars-sur-Glâne), you will be an active member of the Management Committee providing guidance and support to the Management Team and Line Managers of this particular affiliate. You will act locally as a subject matter referent in all HR areas such as Recruitment, On-Boarding, Administration, Compensation & Benefits, Performance & Talent Management. You will be an active and integrated member of Vifor HR Community and you will closely partner with your Global colleagues in Talent Acquisition, Learning and Development and Compensation & Benefits. You will operationally report to the affiliate General Manager and functionally report to the Head of Human Resources Switzerland. Main Responsibilities: Act as a local HR partner for General Manager, Management Team and Line managers Active member of the Country Leadership Team (CLT), involve in strategic discussions and decisions for the Swiss affiliate ) Provide guidance and support to local managers for the administration/support of all annual corporate HR processes; e.g. performance management, promotion, salary increase, bonus, etc. Advice the General Manager on the affiliate organization, in all HR matters Facilitate and coach during change process and critical leadership topics as retention, conflict management, dismissal process, etc... Interface with internal / external experts in case of delicate personal circumstances Act as an HR generalist Ensure effective management of all HR administrative tasks (on-boarding, exit process, work certificates, work confirmation, contracts, time management, archiving, filing, personal data and files, social events, training convention, etc.) Close collaboration with Global Compensation & Benefits team for all relative topics : salary policy, benchmark, package proposals in line with the market and internal practices Compliance: ensure correct handling of workplace policies, procedures and practices in compliance with Employment legislation and regulations Support the Recruitment activities Work closely with the Talent Acquisition team for all the recruitment processes Interview candidates and make the final choice with the line manager Use the assessment tools as defined by Global Learning & development Propose salary and contract conditions to HR Operations Switzerland Make the offer to the candidate Prepare a proper on-boarding with the line manager Support Performance & Talent Management Follow-up IPD process, Development Plans, Career plans with line managers Promote the internal trainings offered through Vifor Pharma academy, global coaching concepts Organize local trainings based on needs and in coordination with Global Talent Management team Qualifications: Fluent in German, French and English Relevant degree in Human Resources or equivalent Pharma market and business know-how Minimum of 5 years related experience in HR in Swiss environment (an additional experience in international HR is an asset) Very good knowledge of Swiss Labor Law and employment principles. Experience working in a dynamic, international environment (fast growing organization)
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15.07.2020

Vifor Pharma

Product Manager Gynaecology - Fribourg

  • Vifor Pharma

  • Switzerland - Villars-sur-Glâne/Fribourg

  • 15.07.2020

  • Vollzeitstelle

We are looking for a Product Manager Gynaecology to join our Marketing team at our Swiss affiliate in Fribourg, Villars-sur-Glâne. You are responsible for the market observation and the product sales results on the Swiss Market. You work closely with our local Medical and Sales Teams as well as with the Global Teams to ensure elaboration and effective implementation of tactical plans. Your contribution to the success of our products is key. Your responsibilities include, but are not limited to, the following: Establish strategies and brand plan for each of your responsible products Planning and delivery of marketing activities Management of sales and promotional budget Lead the customer team (marketing, medical, sales, market access) Effective collaboration with the Global Teams Stay up-to-date on competition and markets Spend at least 10% of the time with clients in the field Systematic stakeholder management Ensure proper training of external service (sales force) of your products Respect and ensure compliance with agreed procedures and permanent/standing orders For this challenging position, we are looking for a person with an entrepreneurial mindset and strong analytical and conceptual skills. In addition, you bring the following profile: University degree in the scientific and/or in business area (such as Economy, Business Administration, Medicine, Pharmacy, Biology or similar) At least 3 years’ experience in pharmaceutical product management Training in Medical Science and/or Marketing German or French as mother tongue with good understanding of the other language Very good knowledge of English is required Experience in relevant indication, i.e. Gynaecology and Hospital know-how is preferred You describe yourself as an innovative, entrepreneurial and reliable person, who likes to work in interdisciplinary teams. Your excellent and convincing communication skills and drive allow you to successfully interact with your customers both internal and external. Autonomous and objective oriented, you love to embrace new challenges and to use your team spirit to fully contribute to the development of Vifor Pharma in Switzerland.
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