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Pharmazie: 11 Jobs in Eschweiler

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Pharmazie

QC Manager (m/f/d)

Sa. 28.11.2020
Aachen
PAION is a publicly listed specialty pharmaceutical company focused on developing and commercializing innovative drugs for out-patient and hospital-based sedation, anesthesia and critical care services. PAION’s lead compound is remimazolam, an intravenous, ultra-short-acting and controllable benzodiazepine sedative/anesthetic. Remimazolam is partnered in multiple territories outside of Europe. Remimazolam was approved in the U.S. for procedural sedation in July 2020 and was approved in Japan for general anesthesia in January 2020. In China, licensee Yichang Humanwell received market approval in procedural sedation in July 2020 and in South Korea, licensee Hana Pharm filed for market approval for remimazolam in general anesthesia in December 2019. In Europe, PAION is seeking approval of remimazolam for general anesthesia and for procedural sedation. PAION submitted a Marketing Authorization Application (MAA) for procedural sedation in November 2019. Results of a Phase III trial in general anesthesia are expected in the second half of 2020. Together with PAION QA, review QC documentation and QC-related parts of manufacturing and ensure manufacturing / testing activities are conducted in-time and in accordance with current GMP guidelines, PAION specifications and PAION procedures. Drawing up of Specifications in coordination with relevant PAION departments and CMOs  Perform Life Cycle Management of analytical methods by establishing and executing an analytical method validation master plan and follow up of required periodical and ad-hoc measures in cooperation with other departments and PAIONs CMOs. Review and update / improve analytical methods as appropriate, including changes / updates of pharmacopoeia’s methods (Ph.Eur., USP and other). Ensure overall compliance of PAION with ICH requirements, especially ICH Q1, ICH Q2 and ICH Q6  Manage samples and reference materials together with Supply Chain and external partners Manage QC related change controls and deviations internally as well as externally with PAIONs vendors. Provide support to PAION’s licensees in QC related topics where applicable, including the organisation and support of method transfer programs. Draw up, review and maintain internal and external QC-related documents i.e. validation reports, shelf life justifications as well as SOPs. Provide technical support with the drawing up and maintenance of PAION's registration documentation. General management and control of external vendors of PAION and co-ordination of interactions with these vendors in all QC related topics. Provision of subject matter expertise to support audit of manufacturing / testing facilities in accordance with GMP, current guidelines and PAION procedures.  Master degree / Diploma or ideally a post graduate in Pharmacy, Pharmaceutical Sciences, Chemistry or Life Sciences, preferably with a focus on analytical methods / analytical chemistry At least 5 years practical industrial experience working in pharmaceutical or biotechnology industries and in three or more of the following areas associated with industrialization and manufacturing of pharmaceutical products: analytical method's development and validation, method lifecycle management, quality control, stability testing with a focus on analytical chemistry. Deep-rooted knowledge of regulatory requirements, including ICH requirements and national EU / US regional requirements like national pharmacopoeias (analytical method development and validation (ICH Q2), QC analysis, method lifecycle management). Proven knowledge of Good Manufacturing Practises and of working within a Quality Management System. Experience in managing change controls, deviations and OOS. Proven Experience with commercial manufacturing and on-time release of API and drug products as technical expert in cooperation with a QA team. Proven knowledge of method validation. Knowledge of risk management Fluent in English and German Desired skills: Knowledge of additional national regulatory requirements outside EU / US (e.g. Japan, Korea, Brazil) as well as their national pharmacopoeias Experience of technical managements and direction of external vendors would be extremely beneficial as the company works with a network of vendors. Additional experience in microbiological and sterility testing
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Medical Science Liaison Manager (m/w)

Fr. 27.11.2020
Köln, Kaiserslautern, Saarbrücken, Trier, Koblenz am Rhein, Bonn, Aachen
Vifor Pharma Group, formerly Galenica Group, is a global specialty pharmaceuticals company that researches, develops, produces and markets its own pharmaceutical products and is the partner of choice for innovative, patient-focused solutions. The company’s goal is to be a global leader in iron deficiency, nephrology and cardio-renal therapies and strives to help patients around the world with severe and chronic diseases to lead better, healthier lives. Vifor Pharma Group has production sites in Switzerland and Portugal as well as a dynamic network of affiliates and partners offering broad market coverage all over the world. The company has an ever-growing global presence while at the same time remaining firmly rooted in its home market, Switzerland. Vifor Pharma Group consists of Vifor Pharma; Vifor Fresenius Medical Care Renal Pharma, its joint company with Fresenius Medical Care; Relypsa; and OM Pharma. Medical Science Liaison Manager - Köln, Kaiserslautern, Saarbrücken, Trier, Koblenz, Bonn, Aachen Ort: Germany - Field based Funktion: Medical Affairs Firma: Vifor Pharma Senioritätslevel: ManagerWe are searching for a Medical Science Liaison Manager for the region Köln, Kaiserslautern, Saarbrücken, Trier, Koblenz, Bonn, Aachen. In this position, you will represent Medical Affairs externally to establish and maintain medical relationships with Key Opinion Leaders (KOLs), 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 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 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.
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Head DMPK (m/f/d)

Do. 26.11.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 36976 Head DMPK (m/f/d) Research & Development Aachen published 08.10.2020 Head DMPK (m/f/d) You are accountable for developing DMPK strategies to build a portfolio of high quality clinical candidates, including translational PKPD understanding from non-clinical models, leading to a prediction of clinical pharmacokinetics, efficacious and tolerable dose/schedules and  potential drug-drug interaction profile and interpreting clinical studies You lead and develop DMPK team to support lead optimization, IND-enabling programs and clinical PoC You ensure in time delivery of preclinical and translational DMPK work package from early drug discovery to launch and life cycle management You establish DMPK strategies that align with program goals and strive for high quality clinical candidates You integrate CRO DMPK/PD, bioanalytical, and biotransformation data to address key issues and enable informed, timely decision making You design, manage and review CRO preclinical studies to understand  DMPK profile of candidates to influence discovery decisions and support IND-enabling studies and clinical development You drive human dose projection calculations and support clinical pharmacology trial design based on DDI risk analysis based on nonclinical data and refining based on clinical data You demonstrate high proficiency across a wide range of in vitro/ in vivo DMPK technologies and being capable of initiating new areas of investigation that are scientifically meaningful in supporting drug discovery and development programs You hold a PhD in Drug Metabolism/ Pharmacokinetics or related discipline You have several years of relevant experience in DMPK with several years of experience as a line manager in drug discovery and development with track record of taking molecules to the clinic and beyond You have a track record of developing and leading a strong scientifically data driven DMPK team to support both research and clinical stage programs You have a broad understanding of various DMPK relevant areas such as physicochemical properties, drug metabolizing enzyme & transporter kinetics, pharmacokinetics, mechanistic biotransformation, analytical sciences and PK/ dose modelling You are experienced in interpreting met-id data and proposing metabolic pathways across species You have extensive experience in managing CROs, GLP and other regulated activities You have outstanding problem-solving skills, with proven ability to integrate across disciplines to address issues and identify mitigation strategies
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DMPK Scientist (m/f/d)

Do. 26.11.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 37035 DMPK Scientist (m/f/d) Research & Development Aachen published 08.10.2020 DMPK Scientist (m/f/d) You serve as DMPK project representative on global discovery and development programs You provide metabolism and drug-drug interaction guidance to discovery project teams to mitigate issues such as “soft spot identification,” “major metabolites” to enable identification of high quality “first in man” candidates You lead the interpretation of metabolite ID studies conducted at CROs and serve as internal expert on structure elucidation, metabolic pathways and reactive metabolite formation You serve as bio-transformation subject matter expert providing expert guidance on metabolic pathways of small molecules and alternate modalities such as anti-sense oligonucleotides, peptides, etc. You demonstrate high proficiency across a wide range of in vitro/ in vivo DMPK technologies and are capable of initiating new areas of investigation that are scientifically meaningful in supporting drug discovery projects You monitor project progress with CROs and provide timely and valuable guidance to enable studies being executed appropriately You support human dose projection calculations and support clinical pharmacology trial design based on DDI risk analysis based on nonclinical data and refining based on clinical data You hold a PhD in Drug Metabolism/ Pharmacokinetics or related discipline You have demonstrated extensive experience in conducting/ managing DMPK studies (in vitro and in vivo) at CROs You have demonstrated knowledge in interpreting met-id data and proposing metabolic pathways across species You have experience or knowledge in bioanalytical methods and technologies for small molecules and biologics and in biomarker assays You have experience in working and delivering projects within highly outsourced and matrixed environments across diverse geographies and working cultures You have a proven track record in leading and working in teams based upon a matrix reporting You have a broad understanding of various DMPK relevant areas such as physicochemical properties, drug metabolizing enzyme & transporter kinetics, pharmacokinetics, mechanistic biotransformation, analytical sciences and PK/dose modelling You have strong interpersonal, communication, presentation, and negotiation skill
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Head Chemistry (m/f/d)

Do. 26.11.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 36957 Head Chemistry (m/f/d) Research & Development Aachen published 08.10.2018 Head Chemistry (m/f/d) You provide inspirational and proactive  leadership of Drug Discovery Chemistry (Medicinal Chemistry, Synthetic Chemistry and Computational Chemistry) from lead generation through to candidate selection You are responsible for creating and executing a chemistry strategy for drug discovery that ensures the delivery of high quality clinical candidates You are accountable to provide expert functional input to create, advance and deliver a project from target idea to successful proof-of-concept clinical trial You develop strong design solutions to medicinal chemistry challenges in drug discovery You regularly assess developments in the field beyond classical small molecules like e.g. oligonucleotide therapeutics and identify areas for future investment relevant for drug discovery in pain You are responsible to monitor and optimize performance and motivation of internal and external providers to maximize output for the research programs You have several years of industry experience in small molecule drug discovery, including experience in other modalities like PROTAC, oligonucleotide therapeutics, etc. You have a strong track record of scientific innovation in medicinal chemistry and success in delivering high quality clinical candidates You have proven expertise in Synthetic Chemistry/ Medicinal Chemistry/ Pre-clinical Development ranging from target identification to PoC You have a strong knowledge in chemical biology and proven experience of when to use various chemical modalities in drug discovery You are truth seeking and delivery focused, a driven/passionate scientist with strong focus on creating value, problem solving and making things happen You are a can-do person who can take a hands on approach driving projects forward
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Head Toxicology (m/f/d)

Do. 26.11.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 36975 Head Toxicology (m/f/d) Research & Development Aachen published 08.10.2020 Head Toxicology (m/f/d) You lead the Toxicology team and are responsible for all target-based safety assessments, preclinical safety assessments and implement discovery toxicology strategies to enable the progression of optimized drug candidates You develop overall toxicology plans for lead candidates for Ph I to Ph III You provide strategic guidance for project teams and senior management including evaluation of conclusions and potential impact of toxicology results on program and clinical/ regulatory strategy You lead the development of early hypothesis-driven investigation into mechanisms of toxicity for the proactive management of potential safety liabilities and communication of impact to teams You are responsible for the safety strategy and input to multi-disciplinary drug-hunting project teams You represent Preclinical Development on Discovery and Development teams and interface with internal and external colleagues to ensure timely and accurate dissemination of nonclinical safety strategies as well as results to drive the portfolio strategically You monitor toxicology studies; review, summarize, interpret and integrate complex data sets across multiple disciplines; finalize as submission-ready documents for regulatory authorities You address and resolve scientific issues arising in drug discovery/ development programs You hold a PhD in Toxicology or closely related field with several years' experience in a drug discovery/ development setting of a biopharmaceutical company You have a proven track record of making major contributions to the discovery of one or more marketed or in-development medicines, incl. designing, monitoring, and interpreting toxicology studies to support clinical development of candidate therapeutic agents You have expert knowledge of nonclinical data packages needed to support first in human studies, clinical development and product registration You have extensive experience of regulatory toxicology/ pathology You have strategic leadership/ managerial competencies You are familiar with more than one of the following therapeutic modalities preferred: small or large molecules, cell and gene therapy You are a can-do person, problem solver who takes hands on approach to driving projects forward You have expert knowledge of GLP regulations and experience in the oversight of contracted studies
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Biomarker & Imaging Senior Scientist (m/f/d)

Mi. 25.11.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide.  Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion.  As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity.  Join us at Grünenthal, unleash your full potential and help us change lives for the better.  Job fact summary Job ID: 37155 Biomarker & Imaging Senior Scientist (m/f/d) Research & Development Aachen published 05.11.2020 Biomarker & Imaging Senior Scientist (m/f/d) You will be part of a dedicated Translational Medicine team that is responsible for building a deep understanding of drug mechanism(s) of action to facilitate the identification of candidate biomarkers for target engagement and early pharmacodynamic responses (TE/EPR)  You will be responsible for the development of TE/EPR biomarker assays such that they are “fit-for-purpose” with the pipeline status of the project  You will collaborate with the clinical development teams to embed TE/EPR strategies within early clinical development and experimental medicine studies  You will independently design and execute laboratory experiments, apply advanced data analysis, integration and interpretation with an emphasis on providing appropriate context for data and experiments in order to progress projects and/or develop platforms You will provide clear written reports of experiments, position papers and presentations for internal use within Research and as required contribute to the preparation of documentation to support regulatory applications  You are a PhD level scientist with translational biomarker or pharmacology background with several years of translational experience in academia or pharma, preferably in a relevant pain or neurosciences area  You are a committed laboratory scientist with high level of experience in the development of biomarker assays and the application of imaging techniques  You have a detailed understanding of regulatory environment surrounding biomarkers and validation requirements  You have a broad range of complementary skills in cell biology, molecular biology and biochemical techniques to support assay development work
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Head Electrophysiology Science (m/f/d)

Mi. 25.11.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide.  Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion.  As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity.  Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 37135 Head Electrophysiology Science (m/f/d) Research & Development Aachen published 05.11.2020 Head Electrophysiology Science (m/f/d) You will be part of a dedicated team that provides cutting-edge electrophysiology expertise in support of translational sciences and drug development projects  You will be responsible for the design and implementation of high-quality electrophysiology and pharmacology experiments in order to support translational sciences and drug development projects  You will contribute to the internal knowledge and advancement of the electrophysiological expertise across Research  You will provide cross-functional technical and scientific support across a range of internal research projects and external collaborations  You will provide clear written reports of experiments, position papers and presentations for internal use within Research and as required contribute to the preparation of documentation to support regulatory applications  You are a committed lab-based scientist with a PhD in neuropharmacology with extensive experience in electrophysiology (e.g. single cell/automated patch-clamp, multielectrode arrays) applied to isolated cells, in vitro culture systems and tissue sections  You will have post-doctoral experience in academia and/or industry, possibly including translation sciences  You will have experience of working with a range of cells and tissues from both preclinical species and human biological samples  You will have a broad range of complementary skills in cell biology, molecular biology and biochemical techniques  You are truth seeking and delivery focused, a driven/passionate scientist with strong focus on creating value, problem solving and making things happen
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Qualitätsprüfer (m/w/d)

Sa. 21.11.2020
Eschweiler, Rheinland
Willkommen bei West West Pharmaceutical Services, Inc. ist Marktführer bei der Entwicklung und Herstellung von pharmazeutischen Verpackungskomponenten und -systemen zur Verabreichung von injizierbaren Medikamenten. Wir streben nach einer ganzheitlichen Kooperation mit unseren Kunden, von der Produktidee bis zum Patienten und bieten professionelle Unterstützung in der Entwicklung, Umsetzung und Bereitstellung von Produkten, um das Leben von Millionen von Menschen weltweit zu verbessern. West hat seinen Hauptsitz in Exton, Pennsylvania, und unterstützt Partner und Kunden von Standorten in Nord- und Südamerika, Europa, Asien und Australien. Jeden einzelnen Tag werden ca. 112 Millionen Produkte von West genutzt, die dabei helfen, das Gesundheitswesen für Millionen von Menschen auf der ganzen Welt zu verbessern. Für unseren Standort Eschweiler (bei Aachen) suchen wir zum nächstmöglichen Zeitpunkt einen motivierten Qualitätsprüfer (m/w/d) befristet für 1 Jahr. Analytische Überprüfung von Rohgummimischungen (Mischungskontrolle) sowie die Durchführung von visuellen und dimensionalen Prüfungen (Inprozesskontrolle bzw. Endkontrolle) Erfassung der Prüfdaten in SAP und auf der Chargenkarte Sperrung oder Freigabe von Chargen nach Vorgaben in SAP Überprüfung der Chargenkartendokumentation Durchführung von Sonderprüfungen Kalibrierung und Pflege der Prüfgeräte Einhaltung der GMP- und ISO-Richtlinien Unterstützung der Produktion bei Qualitätsproblemen Weiterleitung der Labormuster Technische Ausbildung/Laborausbildung (CTA, Chemielaborant (m/w/d) o. ä.) Hohes Qualitäts- und Sicherheitsbewusstsein Ein hohes Maß an Gewissenhaftigkeit, Zuverlässigkeit und Verantwortungsbewusstsein Erfahrung in der Qualitätsprüfung/Qualitätssicherung Gute EDV-Kenntnisse (Word, Excel, Outlook, SAP) Durchsetzungsvermögen und Entscheidungs­kompetenz Einsatzbereitschaft und Flexibilität Bereitschaft zur Schichtarbeit (3-Schichtsystem, 17‑Schichtmodell) Englischkenntnisse wünschenswert Internationalität – Als amerikanisches Unternehmen leben wir eine globale Zusammenarbeit innerhalb internationaler Strukturen Philanthropie – Wir legen Wert auf eine wertschätzende und freundliche Arbeitsumgebung sowie flache Hierarchien Marktgerechte Vergütung – Wir bieten eine attraktive, marktgerechte Vergütung, einschließlich betrieblicher Sozialleistungen und Einkaufsvorteile Soziales Engagement – Durch diverse von Mitarbeitern organisierte Aktionen unterstützen wir lokale Hilfsorganisationen Mitarbeitervielfalt – Wir bei West schätzen das breite Spektrum unserer Mitarbeiter und Mitarbeiterinnen, das unser Unternehmen ausmacht Sicherheit – Arbeitssicherheit steht bei uns an erster Stelle; wir bieten sichere Arbeitsplätze in einer zukunftsfähigen Branche Entwicklungsmöglichkeiten – Unsere Mitarbeiter und Mitarbeiterinnen profitieren von einem umfangreichen Schulungsangebot sowie einer steten und gezielten Mitarbeiterentwicklung Familienfreundliche Unternehmenskultur – Wir legen Wert auf eine Vereinbarkeit von Privatleben und Beruf; flexible Arbeitszeiten sind für uns selbstverständlich  
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Apotheker*in (m/w/d) in Voll- oder Teilzeit

Fr. 20.11.2020
Herzogenrath
Die Grenzland-Apotheke wurde  im Jahr 199o gegründet und ist  Teil eines kleinen Gesundheitszentrums der Stadt Herzogenrath, Ortsteil Merkstein. In kollegialer  Zusammenarbeit versorgen neben der Apotheke  eine große Hausarztpraxis, eine Gynäkologische Praxis, eine Zahnarztpraxis, eine Krankengymnasitische Praxis , sowie ein orthopädischen Schuhmachermeister die Patienten vor Ort. Neben der Versorgung von zwei Heimen hat die Apotheke eine Zulassung als Sanitätshaus, sodass wir die Patienten in wirklich schwieriger Lebenslage nicht nur mit Arzneimitteln , sondern auch mit Hilfsmitteln versorgen können. Zur Unterstützung unseres Team suchen wir ab sofort oder später eine*n kompetenten und teamfähigen Apotheker*in , die/der sich gerne den Herausforderungen einer Apotheke in einem kleinstädtischen Gesundheitszentrum stellt. die Regelversorgung und Beratung der Patienten*innen die Versorgung der Heimbewohner und die Beratung der Pflegekräfte die Unterstützung der Kolleginnen in der Rezeptur die Beratung der umliegenden Ärzte im Bereich der Wechselwirkungen und Kontraindikationen die Unterstützung des Teams bei der Hilfsmittelversorgung die Vertretung des Apothekenleiters in Urlaubs- und Krankheitsfällen. Voraussetzung: Erhalt der Approbation als Apotheker*in durch eine bundesdeutsche Behörde Zuverlässigkeit Teamfähigkeit Freundlich und Kompetent 5-Tage-Woche übertarifliche Bezahlung Betriebsrente falls gewünscht Kfz-Gestellung Beteiligung bei den Umzugskosten Wechselprämie in Höhe eines Monatsgehaltes 13-tes Gehalt Tankgutschein Unterstützung bei der Wohnungssuche Wir sind Weiterbildungsstätte im Bereich der Allgemeinpharmazie
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