811 Firmen für deine Suche.

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

20.11.2020

Vifor Pharma

Regulatory Affairs Director - China

  • Vifor Pharma

  • China - Beijing

  • 20.11.2020

  • Vollzeitstelle

Are you an experienced regulatory affairs professional with strategic experience of new product registration in China? Vifor Pharma has a newly created opportunity for a Regulatory Affairs Director based in Beijing, China to lead the regulatory function in the local affiliate and drive strategies to accelerate regulatory approval for our product portfolio in China. Key responsibilities Manage, guide and develop the local RA team, ensure planned local regulatory affairs activities are delivered in time and proper local Regulatory procedures and policies are in place. Support Global Regulatory Affairs in accelerating the approval of Vifor portfolio in as a key RA SME for specific considerations related to regulatory frameworks in China. Act as RA lead to develop advocacy, support Authority management with stakeholder mapping and proactively build and strengthen external stakeholder contacts (external experts, industry organizations, etc) in China Develop and evaluate registrations as well as clinical strategies to ensure effective achievement of regulatory/business objectives, approvals, and optimal labels. Act as key regulatory affairs subject matter expert for specific considerations related to relevant strategic objectives regarding Advocacy, functional capabilities, and clinical design strategies. Proactively address industry trends and opportunities, and key regulatory trends related to registration requirements, clinical development and clinical requirements supporting new product approval. Act as primary Vifor RA representative in front of the CDE in collaboration with Global RA International Strategy group. Provide input for GRA International Strategy in interpreting public information related to approval of products and on conditions for building regulatory dossiers to support the safety, efficacy, medical usefulness, and marketability of drug and product candidates in China. Review and ensure that the design and conduct of clinical development programs and individual studies are appropriate to generate data supportive of registration in China. Requirements Advanced degree in pharmaceutical or health related field At least 10-12 years’ experience with regulatory affairs in the pharmaceutical industry (prescription drugs) in China Demonstrated experience managing regulatory strategy and submission of dossiers including study design, data review, approval strategies and labelling negotiations in China Demonstrated experience interacting with local health authority bodies and local health experts Solid knowledge of the Chinese regulatory environment, clinical practice regulations in China Proficiency in Mandarin and English (verbal and written) is essential Experience in pharmacovigilance regulations is a plus Experience in anaemia, nephrology, rare diseases or speciality drug development is preferred
Inserat ansehen

23.11.2020

Vifor Pharma

Medical Science Liaison Manager - Mecklenburg-Vorpommern, Berlin, Brandenburg

  • Vifor Pharma

  • Germany - Field based

  • 23.11.2020

  • Vollzeitstelle

We are searching for a Medical Science Liaison Manager for the region Mecklenburg-Vorpommern, Berlin, Brandenburg. In this position, you will represent Medical Affairs externally to establish and maintain medical relationships with Key Opinion Leaders (KOLs), Health Care Professionals (HCPs) and key accounts on behalf of Vifor Pharma Group. Yours tasks will include the following: Develop and maintain scientific and medical expertise (Indications and products) Identify, develop and maintain relationships with KOLs, HCPs and professional organizations KOL engagement, key account medical support, training and other appropriate activities Facilitate scientific engagement, scientific exchange and medical information Provide clinical presentations and respond to medical requests Update medical team and other internal stakeholders on medical community interactions Support the development, implementation and completion of medical activities (advisory boards, congress symposia, hospital meetings and speaker programs) and attend relevant scientific meetings and conferences Serves as a medical resource for internal medical and sales training Support company sponsored clinical research and IIS process Ensure compliance with applicable local and global laws, regulations, guidelines and company policies and procedures Develop personal and professional capabilities to improve skills and professional capabilities For this role you will need to bring the following requirements: MSc in Medical Field (e.g. Pharmacy, Chemistry or Biology) Minimum of 3 years’ experience in research, pharmaceutical medical affairs or clinical practice Minimum of 3 years’ experience with pharma industry and healthcare compliance requirements locally and globally, ideally in Nephrology Demonstrated experience in KOL, HCP or medical community engagement Excellent oral and written communication skills in German and good oral and written communication skills in English Experience in public scientific presentations We are looking for a strong team player with good communication and networking skills. An entrepreneurial spirit with a humble approach and the ability to influence and persuade stakeholders are important competencies for this role.
Inserat ansehen

23.11.2020

Vifor Pharma

Medical Science Liaison Manager - South East, Nürnberg

  • Vifor Pharma

  • Germany - Field based

  • 23.11.2020

  • Vollzeitstelle

We are searching for a Medical Science Liaison Manager for the South East region. In this position, you will represent Medical Affairs externally to establish and maintain medical relationships with Key Opinion Leaders (KOLs), Health Care Professionals (HCPs) and key accounts on behalf of Vifor Pharma Group. Yours tasks will include the following: Develop and maintain scientific and medical expertise (Indications and products) Identify, develop and maintain relationships with KOLs, HCPs and professional organizations KOL engagement, key account medical support, training and other appropriate activities Facilitate scientific engagement, scientific exchange and medical information Provide clinical presentations and respond to medical requests Update medical team and other internal stakeholders on medical community interactions Support the development, implementation and completion of medical activities (advisory boards, congress symposia, hospital meetings and speaker programs) and attend relevant scientific meetings and conferences Serves as a medical resource for internal medical and sales training Support company sponsored clinical research and IIS process Ensure compliance with applicable local and global laws, regulations, guidelines and company policies and procedures Develop personal and professional capabilities to improve skills and professional capabilities For this role you will need to bring the following requirements: MSc in Medical Field (e.g. Pharmacy, Chemistry or Biology) Minimum of 3 years’ experience in research, pharmaceutical medical affairs or clinical practice Minimum of 3 years’ experience with pharma industry and healthcare compliance requirements locally and globally, ideally in Nephrology Demonstrated experience in KOL, HCP or medical community engagement Excellent oral and written communication skills in German and good oral and written communication skills in English Experience in public scientific presentations We are looking for a strong team player with good communication and networking skills. An entrepreneurial spirit with a humble approach and the ability to influence and persuade stakeholders are important competencies for this role.
Inserat ansehen

18.11.2020

Vifor Pharma

(Senior) Medical Manager Nephrology - Munich

  • Vifor Pharma

  • Germany - Munich

  • 18.11.2020

  • Vollzeitstelle

Für unser medizinisches Team am Standort München suchen wir zum nächstmöglichen Zeitpunkt einen erfahrenen Medical Manager Nephrologie (m/w). Sie berichten an den medizinischen Direktor bzw. an den Head of Medical Affairs. Der Schwerpunkt der Tätigkeit liegt im Bereich der Hämodialyse. Sie sind unter anderem für folgende Aufgaben zuständig: Erstellen und Umsetzen der medizinischen Strategie für das Nephrologieportfolio Eigenverantwortliche Durchführung von medizinischen Advisory Boards, Kongresssymposien, Fachpublikationen, Fortbildungen, etc., wie auch bestehende und neue wissenschaftliche Forschungsvorhaben erfolgreich auf den Weg zu bringen, mit Fokus auf Real World Data Generation Beantwortung von medizinischen Anfragen und wissenschaftlicher Informationsdienst aller von der Vifor Pharma Deutschland vertriebenen Produkte Erstellen der medizinischer Argumente im Rahmen von Frühberatungen und/oder des Value Dossiers im Rahmen der frühen Nutzenbewertung neuer Medikamente Enge Zusammenarbeit mit den Bereichen Marketing und der Business Unit Nephrologie durch Einbringen der medizinischen Perspektive bei der Erstellung von Kommunikations-Unterlagen in Zusammenarbeit mit dem jeweiligen Produktmanager Planung und Durchführung von fachlichen Schulungen für interne Kollegen Für diese Position suchen wir eine Fachexpertin/einen Fachexperten im Bereich Nephrologie mit einer strukturierten, wissbegierigen und kommunikativen Persönlichkeit zu folgendem Profil: Erfolgreich abgeschlossenes Studium der Humanmedizin (oder Pharmazie), idealerweise mit abgeschlossener Promotion und klinischer Erfahrung im Bereich Nephrologie/Dialyse Erfahrung in der pharmazeutischen Industrie, möglichst im medizinischen Fachbereich oder einer vergleichbaren Position; Erfahrung in der Produktneueinführung wünschenswert Erfahrung im Bereich Real World Data Generation Kenntnisse der relevanten gesetzlichen Regulatorien, z.B. Arzneimittelgesetz, Good Clinical Practices, Good Pharmacovigilance Practices Fliessende Deutsch und Englischkenntnisse, schriftlich sowie mündlich; überzeugende Präsentationsfähigkeit in beiden Sprachen Hohe intrinsische Motivation sowie proaktives Einbringen eigener Ideen gepaart mit einem ausgeprägten Pioniergeist Analytische und konzeptionelle Denkweise sowie zielgerichtete, tatkräftige Umsetzung eines medizinischen Aktivitätenplans Hervorragender Teamplayer mit Kommunikations- und Kooperationsfähigkeit Darüber hinaus verfügen Sie über ein hohes Mass an Flexibilität und Selbstmotivation. In Ihrer Persönlichkeit überzeugen Sie durch einen strukturierten und selbständigen Arbeitsstil und sind dabei zuverlässig, team- und ergebnisorientiert und handeln stets nach unseren ethischen Grundsätzen.
Inserat ansehen

09.11.2020

Vifor Pharma

Medical Science Liaison Orphan Disease - Italy

  • Vifor Pharma

  • Italy - Field based

  • 09.11.2020

  • Vollzeitstelle

At Vifor Pharma, due to recent positive clinical trial data for one of our key orphan drugs, we are setting up a new team of Medical Science Liaisons who will support the field medical activities associated with our product for treatment of ANCA Vasculitis. As a result, we have a vacancy for an experienced Medical Science Liaison to join us in Italy. It is an exciting opportunity to be involved in a niche therapy area and be a part of the team taking the product to launch. Responsibilities As an MSL, you will be responsible for the following: Develop and maintain scientific and medical expertise (Orphan disease areas) Identify, develop and maintain relationships with KOLs, HCPs and professional organisations KOL engagement, key account medical support, training and other appropriate activities Facilitate scientific engagement, scientific exchange and medical information Provide Disease State Education, clinical presentations and respond to medical requests Update medical team and other internal stakeholders on medical community interactions Provide medical support for patient and formulary access following global and local policies and procedures including liaison with patient associations Support the development, implementation and completion of medical activities (advisory boards, congress symposia, hospital meetings and speaker programs) Serves as a medical resource for internal medical and sales training Support company sponsored clinical research and IIS process Attend relevant scientific meetings and conferences and support development of summaries of key data, presentations or symposium Ensure compliance with applicable local and global laws, regulations, guidelines and company policies and procedures Requirements As a Medical Science Liaison, you will need to demonstrate the following skills and experience: Deep therapy area knowledge in nephrology, rheumatology or autoimmune diseases Demonstrated experience in KOL, HCP or medical community engagement Experience in literature review and analysis Excellent oral and written communication skills Experience in public scientific presentations and experience in planning and delivering medical trainings Experience gained in the pharmaceutical industry and a strong understanding of the healthcare compliance requirements locally and globally Strong communication skills and fluency in Italian and English Educational qualifications: Doctoral level degree (MD, PharmD or PhD) or MSc in Medical Field (e.g. Pharmacy, Nursing, Chemistry or Biology) with experience in clinical practice, research or pharmaceutical medical affairs within Nephrology, Rheumatology or Autoimmune disease Availability to travel up to 50% of the time is a must. If this opportunity is of interest to you, please apply by submitting your application including your updated CV.
Inserat ansehen

10.11.2020

Vifor Pharma

Medical Science Liaison Italy - Sicily and Calabria

  • Vifor Pharma

  • Italy - Rome

  • 10.11.2020

  • Vollzeitstelle

Due to internal progression, Vifor Pharma has an excellent opportunity for a Medical Science Liaison to join our affiliate in Italy. As a part of our medical affairs team, the Medical Science Liaison will defend Vifor Pharma's interests in iron deficiency anemia, cardiorenal and nephrology. The territory includes Sicily and Calabria. Ideally, the candidate will need to based in one of the following areas: Messina, Catania, Palermo, Reggio Calabria, Lamezia Terme Key responsibilities: Serve as scientific expert for internal and external customers Ensure dissemination of medical information and partner with key influencers and capture insights and opportunities for Vifor Pharma Development of presentation material for clinical sessions, advisory boards, investigators meetings and training Development of trial related documents All activities related to planning, execution and reporting of clinical trials in coordination with external vendor Build strong network with medical/nurse societies Train internal people in the Italian affiliate Speaker about our products in scientific meetings All activities related to planning, execution and reporting of clinical trials / registries national or international in coordination with external vendor. Accountable to represent the Medical Affairs team as an interface with external and internal customers. Requirements: As a Medical Science Liaison, you must have the following profile: PhD or Health related Master Degree, a registered Pharmacist or equivalent Previous experience in a Medical Science Liaison role Experience in cardiology or nephrology therapy area is a plus Ability to travel 60% of the time Fluent in English and Italian Strong presentation and KOL management skills Demonstrable ability to build external and internal relationships through strong communication, influencing and collaborative networking skills. If this opportunity is of interest to you, please apply by submitting your updated CV via our careers portal.
Inserat ansehen

24.11.2020

Vifor Pharma

Head of Signal Management - Geneva or Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 24.11.2020

  • Vollzeitstelle

Are you an experienced pharmacovigilance professional looking for a new challenge? Vifor Pharma has an opportunity for a Head of Signal Management to join their drug safety function. This role can be based in Geneva or Glattbrugg. Responsibilities Ensuring ICH/FDA/ and EMA Guidelines compliance Responsible of the whole process of signal detection and management Responsible, in close collaboration with Drug Safety Lead and Therapy Area Lead, that all tasks relating to Signal detection and management are properly conducted in time Responsible, in close collaboration with Case Management, that data sources for signal detection are available and robust Responsible, in close collaboration with any Service Provider that all subcontracted tasks related to Signal management are properly conducted in due time Acting as key contact point for Signal detection and management Acting as owner of all procedural documents and ensuring regular review and updates Participating to Audits/Inspection as company specialist of Signal detection and management Collaborating with Drug Safety Leads/Therapeutic Area Leads for the implementation and improvement of the process Collaborating with Head Clinical Drug Safety for Signal management in clinical safety data sets Collaborating with Medical Writing Unit for aggregate safety reports writing Medical evaluation of adverse event reports Acting as QPPV for Switzerland as per Drug Authorization Ordinance and Ordinance on Medicinal Products Requirements PhD/ Equivalent with experience in International Drug Safety, ideally operational as well as clinical drug safety Experience in data analysis, signal detection and benefit/risk evaluation Excellent knowledge of international regulations (ICH, Volume 9A/10, EMA GvP ,FDA regulations and Swiss regulations) Fluency in English Knowledge and experience in Pharmacoepidemiology Demonstrated ability to set up and implement drug safety strategies, risk management plans, develop Drug Safety systems and procedures, and elevate and resolve issues. Demonstrated proficiency in problem-solving with respect to pharmaceutical Drug Safety issues. Good computer literacy with experience with safety data bases (ARIS G preferably)
Inserat ansehen

17.11.2020

Vifor Pharma

Head Customer Operations & Demand Management - Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 17.11.2020

  • Vollzeitstelle

In this senior position, you are part of the Global Supply Chain department and report directly to the Head of Global Supply Chain Operations. You are responsible for leading and organizing the Customer Operations & Demand Management Team including appropriate staffing. Your main tasks are the following: Supervise and coach a team of diverse professionals with a multi-cultural background Coordinate and lead the Demand Review Meetings with the regions, maintain an accurate demand plan in IBP demand whilst constantly improving forecast accuracy and monitoring in market stock and safety stock levels Ensuring receipt of the firm orders according to contractual lead times and challenge any major deviations Assess customer orders upon receipt, calculate the products free of charge to be compensated (returns goods expired) monitor and execute on time delivery Review and re-estimate the expected turnover for the regions, circulate and review the numbers with the regional management and conduct a gap analysis versus Budget/re-estimates with various key stakeholders Monthly OTIF Review and departmental KPI reporting, with SCM LST Liaise with department heads around estimates and MTP prior to budget meetings Support monthly S&OP / IBP cycle with data preparation, analysis and mitigate supply risks with supply chain Review Distribution Agreements and provide timely feedback particularly on the operational as well as supply chain sections Further assist Legal, Commercial, Quality, Finance and the joint company VFMCRP that SDEA and QAG agreements are reviewed and signed Coordinate operational management activities in case of new partnerships, partner changes and NPI’s Actively participate in projects with operational impact on the various Regions (e.g. CMO change, regulatory variations, artwork changes, serialization etc.) Conduct review alongside Regulatory department, of all the ongoing and pending activities, potential issues and contribute toward solving them by deriving and proposing contingency plans Annual review with the Region around opportunities to increase the prices/margins, circulate new price lists to partners and internal stakeholders and maintain pricing in the ERP system In coordination with the Region and Finance, propose pricing and volumes for tender participation, collect all the required documentation and ensure follow-up with partners around status of the tender Strong focus on general process and continue improvements throughout the value chain Actively contribute toward favorable DSO rate, maintain dunning process, calculate/issue marketing contribution payments, price compensation for hospital tenders, service fees etc. Participate at Commercial, Finance and Supply chain meetings to review the Budget plan as deemed necessary Ensure trade compliance, collect documentation, import license authorizations in conjunction with the regions Calculate with the Regional M&S Directors, sample needs for own Sales force and exclusive Sales team and ensure availability with Supply Chain at the requested dates Manage the operational relationships with Partners and own Sales Force (Country Managers) thereby ensuring that all contractual commitments of the Distribution Agreement are met Maintain good relationships with internal and external partners and develop a trustworthy environment The ideal candidate has a degree in International Business, Business Administration, Supply Chain or Logistics, in addition to the following skills and experience: 5 - 8 years’ experience in supply chain within the pharmaceutical, biotechnology or medical devices industry Minimum 5 years in a leading role in an international environment, with proven experience a customer service and demand management Green/Black Belt Six Sigma & Supply Chain (APICS/IBF) certification desired Fluent in English and either German or French (written and verbally); Knowledge of any other foreign language is an asset Expert knowledge of ERP systems in particular SAP, SD,MM, FiCo, IBP as well as experience with other programs such as Anaplan, Power BI & MS Office Suite Good understanding of the pharmaceutical industry, GxP and other relevant regulations Ability to influence Director & VP Levels within the organisation and in a matrix environment Ability to utilize business acumen and financial acumen to drive cross-functional decisions You are an influential leader with the ability to engage and influence stakeholders across a matrix environment. You are self-aspired, have a positive “can do” attitude with a vast amount of experience in turning around difficult business situations. On top you are a “cool-headed” great communicator, with the ability to understand issues from multiple perspectives and successfully resolve them. You act as a role model for the Vifor Pharma values.
Inserat ansehen

12.11.2020

Vifor Pharma

Contract Management Associate - Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 12.11.2020

  • Vollzeitstelle

Zur Verstärkung unseres Legal-Teams in Zürich suchen wir eine/n Contract Management Associate. In dieser Funktion rapportieren Sie direkt an den Head of Legal Center of Excellence. Zu Ihren Hauptaufgaben gehören: Elektronische Erstellung / Ausführung / Ablage / Archivierung / Verwaltung von Verträgen Sicherstellen der Datenqualität und -genauigkeit im Vertragslebenszyklus-Management-Tool und in den Vertragsarchiven der Vifor Pharma Erstellung, Pflege und Aktualisierung der Vertragsdatensätze im Vertragsverwaltungstool Integration, Unterstützung und Schulung der Benutzer des Vertragslebenszyklus-Management-Tools und Führung von Aufzeichnungen über die Dokumentschulungen Anbieten von Ad-hoc- und Auffrischungsschulungen für Benutzer Durchführung technischer Wartungen und Aktualisierungen des Vertragslebenszyklus-Management-Tools in Zusammenarbeit mit relevanten internen und externen Funktionen und Anbietern Unterstützung unserer Tochtergesellschaften bei Vertragsanfragen Arbeiten Sie als Teil des Teams, um auf Anfragen in der gemeinsam genutzten Mailbox des Teams zu antworten Erstellung grundlegender Dokumente Unterstützung des Vertragsverwaltungsspezialisten Für diese Aufgabe suchen wir eine kommunikationsstarke Persönlichkeit mit folgendem Profil: Mindestens 3 Jahre Berufserfahrung in einem internationalen Umfeld, bevorzugt in der Pharmaindustrie oder einer ähnlichen Branche (Lebensmittel, Medizinprodukte etc.) Vertiefte Erfahrung in der Verwaltung von Vertragsmanagementsystemen Erfahrung in der Arbeit mit Rechtsverträgen Gute Kenntnisse in MS-Office Fliessende Deutsch- und Englischkenntnisse in Wort und Schrift Für diese Rolle stellen wir uns eine Person vor, die selbständig und exakt arbeitet und proaktiv mitdenkt. Sie bezeichnen sich als durchsetzungsfähig und besitzen ein analytisches und strategisches Denkvermögen. Sie sind dabei kommunikativ, zuverlässig, kontaktfreudig, team- und ergebnisorientiert und handeln stets nach unseren ethischen Grundsätzen.
Inserat ansehen

06.11.2020

Vifor Pharma

Global Scientific Publications Lead - Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 06.11.2020

  • Vollzeitstelle

Are you an experienced scientific publications professional looking for a leadership role in a growing pharma environment? Vifor Pharma is seeking a Global Lead of Scientific Publications (Director) within the Global Medical Team, reporting directly to the Head of Medical Excellence. Within this role you will be responsible for establishing and leading the scientific publications function within the Global Medical organisation. This exciting position is an excellent opportunity to work in a dynamic matrix environment where you will have the responsibility to enhance the organizational capabilities by building the function and driving publications delivery. Key responsibilities (not limited to): Establish a centralised publication function within the Global Medical organisation Direct development and implementation of Global publication plans and deliverables in collaboration with the cross-functional publications team and vendors Lead the regular global publication plan meetings with the cross functional team Act as the key interphase with country affiliates on publications and publication planning Implement and ensure publication policy standards meet international standards and requirements Ensure creation of compliant processes for planning and delivery of publications in collaboration with Legal/compliance, R&D and Medical Develop and champion compliance with publication development, tracking of individual publications and internal procedural documents and guidelines Provide internal expertise in publication planning and execution Manage vendor teams, process and budget Pilot innovation in the field of publications Requirements: Higher degree in a scientific/medical subject preferred (PhD, PharmD) Minimum 10 years of experience in the pharmaceutical industry or a medical communications agency Minimum 5 years in scientific publications, including experience in publication planning, execution and communications Robust understanding of GPP, ICMJE and other relevant publication guidelines Experience with publication management software Key Competencies required: Proven record of leading publication planning, execution and communication Expertise in project management, tracking and reporting Demonstrable expertise in understanding scientific concepts, data interpretation and process development Medical Affairs understanding - management and conduct of studies, evaluation of clinical trial outcomes, medical writing, congress and workshop management, KOL communication Business acumen to collaborate appropriately and compliantly with partners Works effectively in cross-functional teams through proactive communication, collaboration and stakeholder management Can demonstrate organizational effectiveness and time management skills Proven relationship building skills with key opinion leaders, authors and medical affairs/clinical development stakeholders Fluent level in English, both in oral and in written communications If you meet the above mentioned criteria and are interested in this opportunity, please apply by submitting your updated CV via our careers portal.
Inserat ansehen

06.11.2020

Vifor Pharma

Clinical Development Director Cardiorenal - Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 06.11.2020

  • 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

05.11.2020

Vifor Pharma

Clinical Trial Associate - Zurich

  • Vifor Pharma

  • Switzerland - Glattbrugg/Zurich

  • 05.11.2020

  • Vollzeitstelle

We are currently looking for a Clinical Trial Associate to support our Clinical Development team at our operational headquarter in Glattbrugg, Zurich. Reporting to the Clinical Trial Management Director, you will be part of a cross-functional team and contribute to the operational execution of global clinical trials, as well as supporting the performance and quality targets for all Vifor Pharma sponsored studies. Your tasks will include the following: Support operational execution of global clinical trials, from start-up activities until archiving of study documentation Ensure operational support of clinical study teams including creation and distributing of meeting minutes as well as the follow up on open action items Set-up, manage and maintain ICH GCP compliant Trial Master File and support the CST functions in review and audit of vendor Trial Master File to ensure quality compliance Provide input into department SOPs and procedures Be an active member of international internal and external clinical study teams Ensure that trial invoices are processed in a timely manner, maintaining financial records for each study and invoice tracking list For this role we are looking for a flexible and efficient person bringing the following profile: Degree ideally in Life Sciences or equivalent degree; PhD is a plus At least 2 years of experience in clinical trial support in the pharmaceutical industry Familiar with clinical trial documentation and regulatory requirements Understanding of the drug development process and clinical trial execution Good knowledge of ICH GCP requirements Excellent user of Office Programs (Word, Excel, PowerPoint) and MS Project Fluency in English, oral and written Additional language skills (e.g. German, French) are a plus Ability to travel occasionally You bring excellent verbal and written communication skills. Your attitude and entrepreneurial spirit is congruent with the company values. You are interpersonally aware and culturally sensitive, with the ability to work in highly networked organisations with many partners. You are a team player, working well in cross-functional teams, but also being able to work independently. You take a thorough approach with high attention to detail and can think and influence conceptually, strategically and rationally. You are effectively able to plan and prioritise workload, with an accurate sense of urgency. You are an eager learner and can act as a fast-paced, proactive ambassador of Vifor Pharma.
Inserat ansehen

29.11.2020

Vifor Pharma

Master Data Coordinator (limited) - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 29.11.2020

  • Vollzeitstelle

We are currently looking for Master Data Coordinator who will create, maintain and manage Master Data related processes and activities. Based in St. Gallen, you will report to the Global Master Data Manager and your responsibilities will include: Create and maintain the Material Master Data and manage related processes Coordinate cross-functional communication and, if necessary, collect and provide information on demand Ensure master data accuracy Troubleshoot master data-driven system errors Support, guide, and influence other master data users to ensure adherence to global best practices Assist with internal and external audits Monitor, process and control Material Master Data creation and maintenance requests Create and maintain Material Master Data Support all stakeholders involved in Master Data creation and maintenance processes. Obey cross-site Master Data guidelines and processes Provide accurate, homogeneous and high quality data Ensure professional and pro-active flow of information Communicate clearly and accurately with different Stakeholders, both orally and in writing Support setup and maintenance of procedural and Master data governance documents Support SAP relevant projects to improve data quality or workflow improvements We are looking for a proactive- and service-oriented person who brings experience in working with a wide variety of stakeholders across diverse teams. The ideal candidate brings the following skills and experience: High school diploma or apprenticeship in IT or Supply Chain Some experience (1-3 years) working in the pharmaceutical or another regulated industry. 2 years expertise in the use of ERP systems Experience in Master Data Management would be advantageous Excellent command of German and English – both spoken and written, additional language skills are an advantage Detail-oriented, problem solver, ability to perform analysis and validate results Good interpersonal skills Strong communication and organizational skills You have the ability to understand interconnection between the processes and consider the whole picture. Additionally. You bring a proactive approach and are able to work under pressure and to deal with tight deadlines. This is a temporary position. The contract will last from February 1st 2021 to September 30th 2021.
Inserat ansehen

28.11.2020

Vifor Pharma

QA-Manager Quality Systems (Limited) - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 28.11.2020

  • Vollzeitstelle

In dieser temporären Anstellung sind Sie zuständig für die Bearbeitung von GMP-konforme Abläufe zu Dokumenten, Schulungen und Change Control. Zu Ihren Aufgaben gehören: Sicherstellung der GMP-Compliance im Verantwortungsbereich Erstellung und zeitgerechte Aktualisierung von Arbeitsanweisungen (SOPs) Angemessene Schulungen der Arbeitsanweisungen (SOPs) Mitwirken in IT-Projekten zum Verantwortungsbereich (eDMS, LMS,Trackwise) - Gestaltung, Funktionalität testen, Validierung, Maintenace Vertretung der zu verantwortenden Systeme während Behördeninspektionen und Kundenaudits Erfahrungs- und Ergebnisaustausch mit anderen Vifor Pharma Standorten zu den Themenbereichen Dokumente, Schulungen, Change Control Durchführung von Selbstinspektionen und Audits bei externen VIT-/VFMCRP-Partnern Bearbeiten von Änderungsanträgen und Abweichungen zu Prozessen im Verantwortlichkeitsbereich Regelmässige Auswertung, Berichterstellung und Massnahmenfestlegungzu den Dokumentenerstellungen, Archivierung, Dokumentenabgabe,Übersetzungen, -Obsoletsetzungen und kontrollierten Kopien GMP-konforme Abbildung der Schulungen im elektronischen, Datenbanksystem LMS Onboarding & GMP-Training durchführen Jährliche GMP-Schulung durchführen Regelmässige Auswertung, Berichterstellung und Massnahmenfestlegung zu Change Control Um diese Herausforderung erfolgreich zu meistern, bringen Sie folgende Erfahrung und Kompetenzen mit: Ausbildung an einer Universität oder einer Fachhochschule mit Abschluss im naturwissenschaftlichen Bereich Berufliche Erfahrung in der Wirkstoff- oder Pharmaproduktion Erfahrung in der Qualitätssicherung im GMP-Bereich Erfahrung mit Abweichungen, CAPAs Risikomanagement/Audits von Vorteil Fliessende Deutschkenntnisse in Wort und Schrift, gute Englischkenntnisse Sind Sie eine motivierte und belastbare Persönlichkeit, welche gerne im Team arbeitet und über eine selbständige Arbeitsweise verfügt? Dann freuen wir uns auf Ihr komplettes Bewerbungsdossier (Motivationsschreiben, Lebenslauf, komplette Arbeitszeugnisse und Diplome). Die Stelle ist befristet ab sofort bis 30. November 2021 (12 Monate).
Inserat ansehen

27.11.2020

Vifor Pharma

Supply Chain & Serialization Specialist - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 27.11.2020

  • Vollzeitstelle

In this position, you are responsible for the Global Vifor Serialization System (VSS) and process including the global business process and partners. You report directly to the Team Lead Supply Chain & Serialization. Your main tasks are the following: Plan and manage global serialization, track&trace changes and projects from the business side in close collaboration with the Serialization Project Team and IT, across sites and aligned with all stakeholder and in line with the company strategy Responsible together with the stakeholders and IT for the contract(s) and performance of the VSS providers Responsible that the VSS users are able to perform the tasks by providing guidance, knowledge, training and overall support Manage global documentation Lead and drive meetings between global and local stakeholders and create alignment regarding the use of the VSS and linked processes Support local stakeholders in optimizing the use of the VSS and linked processes EU alert management Troubleshooting in VSS Ensure access to relevant information in SAP which are relevant for artwork creation 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: Bachelor’s degree in Engineering, Supply Chain, Packaging & Production or directly related fields Minimum 3 years of experience in the Consumer Industry and or Pharmaceutical industry with knowledge of quality and regulatory guidelines especially in regards to serialization Minimum 1 year of experience in leading projects in the Pharmaceutical industry Experience with serialization systems Experience with writing and maintaining SOPs Proficiency in use of MS office (Excel, PowerPoint, Visio) Fluency in English and either German or French language You describe yourself as a 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

27.11.2020

Vifor Pharma

Planner / Buyer - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 27.11.2020

  • Vollzeitstelle

For our location in St. Gallen we are looking for an operational Planner / Buyer. In this function you report directly to the Head Supply API & In-house Packaging. You will be responsible for carrying out production planning and independently procure the direct materials needed for production. Your responsibilities will include, but not be limited to: End-to-end supply chain process - from customer order, from sourcing to delivery for shipment Optimum ordering and reordering from suppliers and/or own controlled manufacturing sites in order to fulfil on time in full (OTIF) the customer demand Control and track the correct settlement of deliveries and invoices including the correct archiving of documentation Manage inventory levels to minimize supply chain risks and optimise the OTIF and support in defining the tactical planning Mitigate risks by managing bridging stock according VP category management Maintain master data in the ERP system Build sustainable relationships at peer level with suppliers and internal stakeholders (e.g. Quality, Production, Regulatory and Sales & Marketing) Responsible for the Planning Forecast and alignment with the supplier Prepare and provide monthly reports to the respective departments (e.g. Inventory reporting) For this position we are looking for the following profile: Commercial education or equivalent; preferred a degree and certificate in supply chain management At least 3 years of experience in planning and procurement Understanding of the Pharmaceutical Industry or related (e.g. Food, Chemical, Medical Devices) Experience with SAP-System GMP and/or GDP experience Advanced expertise in MS Office, especially MS Excel Highly analytical skill set with aptitude for figures and data-driven argumentation Fluent in English and German language – both verbally and written You describe yourself as a resilient and responsible person with distinctive teamwork and strong communication skills. You have the ability to work under pressure with an independent work style. Your experience in the field of SCM and your practice-oriented way of working ensure that you always have an overview and a pragmatic solution even in hectic situations.
Inserat ansehen

25.11.2020

Vifor Pharma

SAP Business Expert SD - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 25.11.2020

  • Vollzeitstelle

We are currently looking for an SAP Business Expert SD (Sales and Distribution) to join our Supply Chain SAP Support Excellence team in St. Gallen. In this role, reporting to the Team Lead CoE SAP Support, you will be accountable for coordinating and supporting the overall Tech Ops project scope for implementation and realization of topics related to Sales and Distribution (including maintenance in the post go-live phase). Your tasks will include: Act as a subject matter expert for S/4 SD and associated systems and processes Ensure business requirements are identified, documented, tested and trained for SAP S4/HANA for the SD stream Design own maintenance and project-tasks, define and implement S/4 solution and deliver user requirements and enhancements Drive delivery of harmonised standards for SD related master data, securing the integrity and quality of data Support user training and qualification documentation and training delivery Ensure that outstanding project management, process implementation and design requirements and/or issues are being addressed for projects assigned Communicate activities and status of each project assigned throughout its life cycle Schedule and lead SD-related workshops and meetings as required Identify areas to harmonize, simplify and optimize Ensure required user support is in place Escalate project changes and decisions that exceed decision power to the project management 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 Supply Chain Management, Operations Management, Logistics or Business Administration Minimum 5 years of experience in one of the Tech Ops functions (Sales, Distribution, Logistics) within the pharma industry or similar industry (i.e. food, medical devices, FMCG) Minimum 3 years’ experience with ERP in one or multiple modules with the focus on operations (Material Logistics, Material Management etc.) Proven project management experience/ track record Fluent in English (written and verbally) The following skills would be advantageous: Additional language skills in French or German Working experience in the Pharmaceutical industry or related highly regulated processing industries (e.g. Chemical) 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

22.11.2020

Vifor Pharma

Graduate Program Technical Operations - Limited - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 22.11.2020

  • Vollzeitstelle

Launch your talent and have an impact on our mission to help patients around the world with severe and chronic diseases lead better, healthier lives! Vifor Pharma is offering you the great opportunity to participate in our 2 year Graduate Program within Technical Operations, where you will get an insight into 4 different departments at 2 different sites (St. Gallen and Lisbon). The earliest start is between January and March 2021. This exciting program includes the following: Rotating assignments in key functions within Technical Operations: Supply Chain Management, Manufacturing/ Production, Quality Assurance (QA)/ Quality Control (QC), Technical Project Management Cooperation at different locations The opportunity to interact with various functions and sites Regular mentoring sessions with your sponsor Opportunity to join us for an unlimited contract in a first Managerial role after successful completion of the Graduate Program For this responsible position, you should bring the following profile: Graduate (BSc/ MSc/ PhD) in Life Sciences (e.g. pharmaceutical studies, biology, chemistry, preferably bioengineering) First insight into the industry (e.g. during internships in pharma industry), but max. 2 years of experience (incl. internships) Fluency in English (oral and written) Fluency in German OR French, good knowledge of the other language You have a high learning capability and the ability to think outside the box, linking ideas and concepts. You are an excellent team player with very good communication skills as well as very good organisation and planning skills. With this opportunity you can apply your theoretical knowledge and gain first practical experience in different areas of a rapidly growing, global pharmaceutical company.
Inserat ansehen

16.11.2020

Vifor Pharma

MES Process Manager - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 16.11.2020

  • Vollzeitstelle

Zur Verstärkung unseres lokalen MES-Teams am Standort St. Gallen suchen wir einen MES Process Manager. In dieser Funktion sind Sie Teil des globalen Vifor MES Core Teams und rapportieren direkt an den MES Program Leader. Zu Ihren Hauptaufgaben gehören: Implementierung eines MES Systems - in Zusammenarbeit mit dem globalen Vifor MES Core Team - am Standort St. Gallen sowie an anderen Standorten Projektmanagement und Prozessimplementierung für den Standort St. Gallen Planung, Vorbereitung und Durchführung von Validierungsaktivitäten Erstellung von GMP-Dokumentationen und Change Management Identifikation von Bereichen zur Harmonisierung, Vereinfachung und Optimierung Abhalten von Benutzerschulung und Qualifikation gem. GMP-Anforderungen Planung von Workshops und Besprechungen nach Bedarf Ausbau von Know-how, um ein Kompetenzzentrum für MES innerhalb von Vifor Pharma zu werden In dieser Rolle arbeiten Sie in einem kleinen Team, weshalb wir uns an eine/n Teamplayer/in wenden. Ausserdem bringen Sie die folgenden Anforderungen mit: Abgeschlossenes technisches Studium Mindestens 5 Jahre Berufserfahrung in der Pharmaindustrie oder einer ähnlichen Branche (Lebensmittel, Medizinprodukte etc.) MES-Erfahrung, bevorzugt Werum PAS-X Berufserfahrung in einer IT-Umgebung, in Prozessharmonisierung und -optimierung Erfahrung im Projekt- oder Change Management von Vorteil Gute Englischkenntnisse in Wort und Schrift Für diese Rolle stellen wir uns eine Person vor, die selbständig und exakt arbeitet und proaktiv mitdenkt. Sie bezeichnen sich als durchsetzungsfähig und besitzen ein analytisches und strategisches Denkvermögen. Sie sind dabei kommunikativ, zuverlässig, kontaktfreudig, team- und ergebnisorientiert und handeln stets nach unseren ethischen Grundsätzen.
Inserat ansehen

16.11.2020

Vifor Pharma

Lehrstelle Chemie- und Pharmatechnologe EFZ 2021 – St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 16.11.2020

  • 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

15.11.2020

Vifor Pharma

Chemical Engineer - Befristet auf 1 Jahr - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 15.11.2020

  • Vollzeitstelle

Zur Unterstützung unseres Technical Operation Teams in St. Gallen suchen wir zum nächstmöglichen Zeitpunkt einen Chemical Engineer (m/w). Diese Einstiegsstelle ist befristet für ein Jahr. Sie unterstützen dabei die sichere, ökonomische und termingerechte Herstellung von pharmazeutischen Wirkstoffen und unterstützen den Head of Production in seinen Aufgaben. Zu Ihren Aufgaben gehören unter anderem: Mitarbeit bei technischen Projekten und Validierungen Definition und Umsetzung von Änderungen und Verbesserungen im Produktionsablauf Betreuung der anstehenden Produktionen sowie termingerechte Bearbeitung von Abweichungen vom normalen Produktionsablauf gemäss cGMP Guidelines Mithilfe bei der Evaluation, Bestellung, Qualifizierung und Integration in die laufenden Prozesse von neuen Apparaturen und Betriebsmaterialien Durchführung von Schulungsprogrammen für die Mitarbeiter der Produktion (Beispiel: Trainieren von neuen SOP’s und Prozessabläufen) Betreuung und Wartung von betriebsrelevanten SOP’s hinsichtlich Aktualität und Inhalt Sie sind eine teamorientierte und integre Persönlichkeit mit folgendem Profil: Bachelor- oder Masterabschluss, bevorzugt mit Fokus Chemieingenieurswesen, Chemische Verfahrenstechnik, Bioingenieurswesen oder Prozesstechnik Idealerweise Erfahrung mit chemischen Produktionsverfahren und Erfahrung mit Projektarbeit Hohe Leistungsbereitschaft und starker Wille zur Verbesserung von Betriebsabläufen Fliessendes Deutsch und Englisch in Wort und Schrift Vertrautheit mit den Grundbegriffen des cGMP ist von Vorteil Sie bringen eine starke Kommunikationsfähigkeit und hohes Durchsetzungsvermögen mit sich und überzeugen durch eine initiative und proaktive Ausführung der operativen Aufgaben. Sie bringen einen strukturierten Arbeitsstil mit und haben Spass daran, neue Ideen einzubringen und Lösungen mit zu entwickeln. Wir bieten ein spannendes und angenehmes Arbeitsumfeld, welches die persönliche Weiterentwicklung fördert und in dem freundlicher und respektvoller Umgang mit den Mitarbeitern zentral sind.
Inserat ansehen

06.11.2020

Vifor Pharma

Metrology Transport & Temperature Monitoring Specialist (Limited) - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 06.11.2020

  • Vollzeitstelle

Zur Verstärkung unseres Quality Teams am Standort St. Gallen suchen wir zum nächstmöglichen Zeitpunkt eine/n Supervisor/in in der Metrologie. Diese Stelle ist befristet auf 12 Monate. Sie unterstützen dabei die Temperaturüberwachung von pharmazeutischen Wirkstoff- sowie Arzneimitteltransporten weltweit sowie das Klima-Monitoring am Standort. Zu ihren Aufgaben gehören unter anderem: Temperaturüberwachung von Transporten gemäss GDP GxP- konforme Dokumentation Kommunikation mit internen und externen Partnern Erstellung und Aktualisierung von Dokumenten (SOPs) für den eigenen Arbeitsbereich Mitarbeit bei Transportqualifizierungen sowie Projekten im Arbeitsbereich Administration und Betreuung des Temperatur-Monitoringsystems Auswertung klimatischer Daten Kalibrierung von Temperatur und Feuchtesensoren Verwaltung von Prüfmitteln im LIMS Erstellen von Abweichungen Sie sind eine teamorientierte und integre Persönlichkeit mit folgendem Profil:Chemiker HTL/Chemielaborant mit Berufserfahrung oder Weiterbildung bzw. höherer naturwissenschaftliche Ausbildung Bereitschaft neue Prozesse und Änderungen umzusetzen Sehr gute Deutsch und Englisch Kenntnisse in Wort & Schrift Computeraffinität von Vorteil (Verwenden von diversen Softwaren, wie MS Office, LIMS,Smartview, Monitoring Software, SAP, etc) Idealerweise Erfahrung im GxP Bereich Für diese Rolle stellen wir uns eine Person vor, die sehr gut kommuniziert, selbständig und exakt arbeitet, proaktiv mitdenkt und belastbar ist.
Inserat ansehen

03.11.2020

Vifor Pharma

Head Product Group (m/w) - St. Gallen

  • Vifor Pharma

  • Switzerland - St Gallen

  • 03.11.2020

  • Vollzeitstelle

Für unseren Produktionsstandort in St. Gallen suchen wir eine engagierte Persönlichkeit als Produktgruppenleiter/in. In dieser Führungsfunktion sind Sie verantwortlich für einen Teil der Produktion und rapportieren direkt an den Leiter der Produktion. Zu Ihren Aufgaben gehören unter anderem: Verantwortung für die Herstellung von pharmazeutischen Wirkstoffen, intermediates und Rohstoffen unter Einhaltung der GMP Richtlinien Projektdurchführung im interdisziplinären Team von Forschung, Entwicklung, Technik, Qualitätskontrolle, Qualitätssicherung, Registrierung und Logistik, insbesondere zum Ausbau von Kapazitäten und zur Effizienzsteigerung Weiterentwicklung der Digitalisierung in der Produktion unter Einhaltung der Data Integrity Guidelines und der dazugehörenden Entwicklung der Mitarbeiter Arbeiten und Führen nach den Prinzipien von Operational Excellence Sichere, ökonomische und termingerechte Produktion in der geforderten Menge und Qualität Umsetzen der Vorgaben (Produktionsplan, Sicherheitsanweisungen, SOP’s etc.) in der Produktion Erstellung, Betreuung und Pflege betriebsrelevanter SOPs hinsichtlich Aktualität und Inhalt Betreuung, Aufsicht und bei Bedarf praktische Mithilfe von Produktionsprozessen Bearbeitung von Abweichungen und Implementierung von Verbesserungen im Produktionsablauf und in der Apparaten-Belegung Evaluation von neuen Apparaturen und Betriebsmaterialien Durchführung von Schulungen der Produktionsmitarbeiter Führung und Weiterentwicklung der Mitarbeiter Für diese Position suchen wir eine erfahrene und ambitionierte Persönlichkeit mit folgendem Profil: Abschluss eines Universitäts-, Hochschul- oder Fachhochschulstudiums als Chemiker/in, Chemieingenieur/in oder im Life Science Bereich Mehrjährige Praxiserfahrung aus einem produzierenden Industriebetrieb (Pharma, Biotech, Nahrungsmittel oder Chemie) Fundierte Erfahrung im GMP Umfeld, idealerweise ergänzt mit Lean / Six Sigma Sehr gute Erfahrung mit SAP und MES (PAS-X by Werum von Vorteil) Projekterfahrung Erfahrung in Personalführung und Organisation der Betriebsabläufe ist wünschenswert Fliessende Deutschkenntnisse und sehr gute Englischkenntnisse Für diese Rolle stellen wir uns eine Person vor, die selbständig und exakt arbeitet und proaktiv mitdenkt. Sie bezeichnen sich als durchsetzungsfähig und besitzen ein analytisches und strategisches Denkvermögen. Sie sind dabei kommunikativ, zuverlässig, kontaktfreudig, team- und ergebnisorientiert und handeln stets nach unseren ethischen Grundsätzen.
Inserat ansehen

11.11.2020

Vifor Pharma

Medical Affairs Manager Nephrology - Fribourg

  • Vifor Pharma

  • Switzerland - Villars-sur-Glâne/Fribourg

  • 11.11.2020

  • Vollzeitstelle

We are looking for a Medical Affairs Manager at our site in Fribourg, Villars-sur-Glâne. In this role you will be directly reporting to the Medical Affairs Team Lead and are responsible for the independent scientific support of products in the field of nephrology and of the various departments in the Rx area. Your tasks as subject-matter expert include, but are not limited to: Answering medico-scientific inquiries (internal and external) Medico-scientific support for marketing in the preparation of promotional materials Strategic contribution to the brand team in close cooperation with the marketing and sales departments Scientific training for field staff Review and evaluation of relevant scientific literature Planning, implementation and support of current and new projects such as clinical studies, market access initiatives and registries Scientific engagement with key experts and the physician community in the field Maintain a strong working relationship with Company Headquarters Organisation of seminars, training events, symposia and advisory boards – face-to-face or in the virtual setting Teaching of scientific topics to Sales, Marketing and other Medical collaborators For this exciting position, we are looking for an entrepreneurial person who wants to prove their analytical and conceptual skills on a daily basis. You are a reliable person and have an independent way of working. Additionally you bring the following profile: A successfully completed Master or doctoral degree in medicine, pharmacy, pharmacology or other natural sciences (preference for PhD or MD) Experience in the healthcare or pharmaceutical industry (e.g. patient experience or Medical Affairs skills) Fluency in English and German is a must, both orally and in written Good knowledge in French Willingness to travel throughout Switzerland and occasionally abroad; at ease with digital formats of customer interactions You complement our team optimally if you love challenges, have a self-starting attitude, enjoy engaging with people and are highly committed. As a person with good communication skills, you also appreciate contributing your strong scientific knowledge on a daily basis and acting as an interface between Vifor Pharma and its customers.
Inserat ansehen