Finden Sie Ihren Job mit nemensis ag

At nemensis ag, we connected thousands of applicants with their dream jobs and gave them the opportunity to develop or re-enter the job market. For our client, an international pharmaceutical company in Basel, we are in search for a Teamleader QA (f/m/d).   Position purpose: - Manage external partners management processes to support departmental portfolio, projects and objectives according to agreed timelines and standards. - Ensure timely qualification of assigned vendors to support the business with GxP services and supplies. - Ensure qualification maintenance of assigned vendors    Responsibilities: - Support a discipline and/or provide a service individually or within a team of as-sociates. May provide functional expertise to Line Unit and other QA Units in area of responsibility. - Write, review qualification relevant deliverables and or/ related tools as per area of responsibility in order to ensure compliance with external partner management procedures and purchasing controls regulations. - Comply with internal and external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidance, SOPs etc.).   Qualifications: - Bachelor/Technician (5 years' pharma exp.) or Master - Fluent in English (oral and written), skills in local site-language (German) are an advantage - Sound scientific, technical and regulatory knowledge in the area of medical devices and pharmaceutical products are key skills. - Good understanding of medical device development activities and regulations as well.   At nemensis ag you are always welcome with your personality, your ambitions and your professional experience. Share your expertise with us and apply now!

At nemensis ag, we have connected thousands of applicants with their dream job and given them the opportunity to develop or re-enter the job market. For our client, an international pharmaceutical company in Basel, we are looking for a Specialist Product Lifecycle Management 100%.   RESPONSIBILITY:The Specialist Product Lifecycle Management is part of the EMEA Regional Portfolio Management Team, reporting into the Assoc. Director, Regional Portfolio Management. The incumbent is responsible for reviewing and owning processes that connect with various functions within MSD to drive supply chain actions arising from Product Launches, Network & Source changes, Regulatory driven artwork changes and Obsolescence for the allocated Customer Business Line. These functions include, but are not limited to, Global, Regional and local Human Health, E2E/Regional Supply Planning, Demand Management, SC Fulfilment, Market Planning, internal / external manufacturing sites, Regulatory Affairs, Global Artwork, Serialization, Master Data, Finance, Global Logistics and Quality. 2. Responsibilities Primary activities include, but are not limited to: Leading cross functional teams, managing complex information flow, coordinating and integrating the functional/ tactical project management activities for New Products Launches, Network Changes, Regulatory driven changes with Artwork impact, Insert Growth and Deletions in close collaboration with Value Chain Management, Global Launch Team, Product Source management, ES-PLM and partner with E2E Planners, EMEA Hub functions, Portfolio Management teams across regions (NA, AP, LA) and stakeholders across divisions (GHH & MRL). Coordinate activities to mitigate risks related to the different milestones across the lifecycle stages including, but not limited to: PLR Approval, Code Creation, Initial RCT update, Forecast Positioning, Artwork Readiness, First Packaging/ Pack-by Readiness, in line with the Regulatory Implementation Definition, last packaging to guarantee successful launch, post approval change or deletion by ensuring system readiness to allow MMD execution Responsible for and providing end to end visibility for all projects within assigned product portfolio to all stakeholders throughout all divisions of MSD (HH, RA, MMD, Merck Leadership) Coordinate activities to mitigate risks related to Artwork Readiness. Liaise with Regulatory Affairs, Artwork Centers and Quality for timely execution Liaise within the ES PLM Team to identify cross functional links & risks driven by PSO initiatives & B2B Deals and drive process improvement initiatives with the global process stewards Design, execute, track and report PLM KPls within Region, (Market & Regional views) mitigating risks to minimize impact to business; participate and provide input to the IBP process (Demand Reviews, Site Supply Reviews) Understand & translate the chemical, formulation and packaging lead times, capacity issues, process reliability issues, sourcing flows, market specific requirements (e.g. TOI, shelf life requirements, etc.). and regulatory issues impacting supply into appropriate risk mitigation actions The incumbent will be responsible for the following lifecycle stage specific activities: New Product Introductions (new pipeline and in-line product launches: Set up launch supply strategy, linked to HH launch strategy. Responsible to lead execution of Launch supply strategy by developing market specific timelines in accordance with supply chain design in partnership with other divisions (GHH & MRL) on Launch Execution and Acceleration. Work closely with RCL's to ensure timely submission/approval of PLR's in required timelines (12-18 months prior to launch) and ensure data quality of Launch Requests by resolving inconsistencies with Stakeholders: VCM Organization, GHH and GRA Owner of the Product Launch Requirements Process for MMD in the EMEA region. Review and Approve PLRs for the EMEA region. Manage market registration samples & coordinates market required stability samples Network & Source Changes: Ensure early engagement with Product Source Management group for robust implementation of Source of supply Changes in EMEA HUB, by translating existing source change project into tangible supply chain system readiness milestones while minimizing impact on service and cost Ensure that Voice of the HUB is captured during the Pre-Chartering Phase. Identify scope of change and analyze impact on resource planning Assessing and influencing target dates from an end‐to‐end perspective Regulatory Driven Artwork Changes: Responsible for the coordination and tracking of Artwork Milestones impacting the EMEA Supply Chain HUB. Tracking and reporting upon the initiatives and projects in the overall portfolio using information available in Regulatory tools Work with project lead to use process toolset to construct, deploy and maintain the methodology which is used to manage large scale initiatives/projects including- Serialization, Corporate initiatives, Divestitures. Execute Phase in/ Phase out of SKUs related with material proliferations required due to Regulatory requirements/ Serialization/ Harmonization Manage the Last Authorized Shipping Date Process for the assigned product portfolio Deletions: Apply the Phase out process to all SKUs issued for deletion through the DDC Process Work with other stakeholders (Supply Planning, Demand Management & Fulfillment, Market Planning, Site Print Coordinators, Finance) to apply the Phase out process that fall out of the DDC Scope Liaise with multiple stakeholders from several areas of the business, including commercial, planning and manufacturing, to understand deletion requests and mitigate inventory at risk. Agree and fix on Target Last Production Date with the site & E2E planning functions based on the Target Last Sales Date provide by the market.    Qualifications and Experience  - Bachelor's Degree Required - preferably Supply Chain or related discipline  - Commercial Apprenticeship of minimum 3 years/ 2-5 years relevant work experience (Product Lifecycle Management/ Supply Chain management/ Supply & Demand Planning/ Manufacturing & Packaging/ Project Management/ Regulatory)  - Experience in a customer facing environments, interfacing w/ functions involved in the regulatory process  - Experience in problem solving and task management; prior experience in project management is an advantage  - Pharmaceutical experience is an advantage.  - Proficient in the use of business software (including MS Excel, MS PowerPoint, MS Project). Working knowledge of SAP (prior experience with Merck MRP systems, practices/principles beneficial)  - Fluent in English  - Basic understanding of Operations, Planning, Regulatory strategy and Business/Financial acumen beneficial. Skill and Role Competencies  - Ability to develop a deep understanding of customer needs, behaviors and goals, to improve overall business outcomes.  - Ability to identify and appropriately build and maintain long-term, sustainable relationships with customers, external stakeholders, and key influencers through a variety of relationship-building approaches, in order to achieve a common goal  - Skill in proactively sharing information to keep others updated and ability to present large amounts of complex information clearly.  - Ability to identify process inefficiencies and adapt and develop work processes

Chemikant/Laborant (m/w/d) 100% Bei nemensis ag haben wir Tausende von Bewerbern mir ihren Traumstellen in Verbindung gebracht und ihnen die Möglichkeit der Weiterentwicklung oder des Wiedereinstiegs ermöglicht. Wir suchen per sofort eine/n pflichtbewussten  Chemikanten/Laboranten für ein spannendes Unternehmen.   Ihre Vorteile: Bei nemensis: - Sie werden während Ihrer Stellensuche permanent durch ein Team (Recruiter und Consultants) betreut - Wir sind seit über 10 Jahren Ihr Fachspezialist in der Vermittlung von Temporär- und Feststellen - Wir pflegen ein grosses Kundennetzwerk in der ganzen Schweiz und bearbeiten spannende Stellen Bei unseren Mandanten: - Grosses, internationales Unternehmen - Festanstellung - Tagschicht/flexible Arbeitszeiten - Unternehmen mit sehr guter Reputation - Selbstverantwortungsvolles Arbeiten - Chancengleichheit   Was Sie machen werden: - Sie sind verantwortlich für den Aufbau von Versuchseinrichtungen - Sie übernehmen die Vorbereitung, Durchführung und Nachbereitung von Kundenversuchen - Sie stellen die einwandfreie Reinigung, Pflege und Wartung der Technikumseinrichtung, wie Rührwerkskugelmühlen und Analyseequipment sicher - Sie arbeiten tatkräftig mit in Entwicklungsprojekten und Tests von Funktionsmustern - Messung der Partikelgrösse, Viskosität sowie farbmetrische und mikroskopische Analyse - Erstellung von aussagekräftiger Versuchsdokumentation in Englisch   Schlüsselqualifikationen: - Sie verfügen über eine abgeschlossene Berufslehre im chemisch-/pharmazeutischen Bereich Chemikant, Chemie- und Pharmatechnologe oder Laborant - Deutsch und Englischkenntnisse in Wort und Schrift - Gute MS Office Kenntnisse - Sie haben Freude am Umgang mit Kunden - Sicheres und gepflegtes Auftreten - Motiviert, teamfähig und selbstständig   Wir freuen uns auf Ihre Bewerbung! Bei der nemensis ag sind Sie mit Ihrer Persönlichkeit, Ihren Bestrebungen und Berufserfahrung immer herzlich willkommen. Zeigen Sie uns Ihre Expertise und bewerben Sie sich noch jetzt. Jasmine Jucker, +41 79 659 98 77, jasmine.jucker@nemensis.com

At nemensis ag, we connected thousands of applicants with their dream jobs and gave them the opportunity to develop or re-enter the job market. For our client, an international pharmaceutical company in Basel, we are in search for a QA -Specialist (f/m/d).   Position purpose: The Quality Assurance Specialist will support the Quality Responsible Person (QRP) as registered contact to the Swiss Health Authorities for quality issues and his Deputy in maintaining an open and transparent relationship with the Health Agency Swissmedic, the Regional Inspectorate, and the Cantonal Health Authority in all distribution matters in Switzerland. As a Quality Assurance Specialist, you will support the implementation of directives issued by the Quality Responsible Person in GMP and GDP matters in the quality interests of our Company's distribution in Switzerland. You will also support the QRP in overseeing the quality systems and processes, in accordance with local and international regulations and internal company standards.   Responsibilities: - Control of batch certificates and comparison with regulatory requirements (approved release specifications, shelf-life, authorized sites involved in the manufacturing process, further regulatory filings etc.) - Record and evaluate results of transport temperature monitoring. - Report temperature excursions and request disposition statements. - Artwork checks. - Process deviations.  - Life-cycle management, administration and change control of standard operating procedures, work instructions, protocols, flow-charts, controlled job aids, and forms according to approved Master SOPs and valid templates. - Formal control of documents in review, support of SOP process owners and authors with structural and formatting rules during creation and review of SOPs. - Implementation of inputs during review of controlled documents. - Processing of Product Quality Complaints (receipt, classification, forwarding to manufacturer, tracking, feed-back to customers, metrics, periodical evaluations). - Timely information of Pharmacovigilance Country Lead in case of suspected AEs in connection with PQCs. - Support processing of quality defects and possible notifications to Swissmedic. - Support planning and monitoring of general GDP training of employees (initial training, GxP-awareness training).   Qualifications: - Master's Degree in in pharmacy, medicine, biology or equivalent. - Minimum of 2-years' experience in Quality Assurance (GMP/GDP) within the pharmaceutical industry. - Documented experience with local Swiss, European and international GxP regulations. - Experience with quality management tools and/or workflow management tools. - English and German language ? Proficiency at a business level. French knowledge is a plus. - Excellent analytical and problem-solving skills, based on science, data and understanding of regulatory requirements in a complex and evolving environment; ability to apply sound risk management. - Team work, communication and solution-oriented.   At nemensis ag you are always welcome with your personality, your ambitions and your professional experience. Share your expertise with us and apply now!

Bei der nemensis ag haben wir tausende von Bewerbern mit ihrem Traumjob verbunden und ihnen die Möglichkeit gegeben, sich weiterzuentwickeln oder wieder in den Arbeitsmarkt einzusteigen. Für unseren Kunden, ein internationales Pharmaunternehmen in Luzern, sind wir auf der Suche nach einem Payroll Administrator (w/m/d).   Aufgaben: - Unterstützung in der fristgerechten Abwicklung der Lohnbuchhaltung   - Selbständige Bearbeitung der eingehenden Lohnmutationen,  Bearbeitung und Unterstützung in lohnrelevanten Prozessen - Abwicklung, Meldungen und Abrechnungen bei Krankheiten und Unfällen - Bearbeitung der Kinder- und Ausbildungszulagen Anträge und Änderungen - Beratung der Mitarbeitenden in Lohn- und Sozialversicherungsfragen, sowie bei Unfall und Krankheit - Bearbeitung von Statistiken, Reports und Auswertungen - Korrespondenz mit den Sozialversicherungsträgern, Steuerämtern und anderen Behörden - Mithilfe Prozessdokumentation sowie stetige Prozessoptimierung innerhalb der Personal ? Lohnadministration - Diverse fachspezifische administrative Aufgaben sowie Mitarbeit bei Projekten - Monitoren des QST Prozesses sowie erstellen der PPR's, Führen von Differenzlisten Profil: - Abgeschlossene kaufmännische Grundausbildung - Abgeschlossene Weiterbildung als HR Sachbearbeiter / HR Fachmann / - frau oder äquivalente Weiterbildung - Einige Jahre Berufserfahrung in einer vergleichbaren Tätigkeit, Arbeitserfahrung in einem Grossunternehmen von Vorteil - Zahlenflair, rasche Auffassungsgabe und pro aktive Arbeitsweise - Sehr gute Anwenderkenntnisse von MS-Office ( Excel, Word, Outlook) - Teamgeist und eine hohe Dienstleistungsorientierung - Stilsicheres Deutsch und sehr gute Englischkenntnisse   Wir freuen uns auf Ihre Bewerbung! Bei der nemensis ag sind Sie mit Ihrer Persönlichkeit, Ihren Bestrebungen und Berufserfahrung immer herzlich willkommen. Zeigen Sie uns Ihre Expertise und bewerben Sie sich noch jetzt. Mirjam Hachen, mirjam.hachen@nemensis.com

Bei nemensis ag haben wir Tausende von Bewerbern mir ihren Traumstellen in Verbindung gebracht und ihnen die Möglichkeit der Weiterentwicklung oder des Wiedereinstiegs ermöglicht. Wir suchen per 01.07.2021 eine/n Mechanical Engineer für ein spannendes Unternehmen im Kanton Luzern.   Verantwortlichkeiten: - Sie handeln und steuern das Projekte im Auftrag den Leiter Engineering - Gesamtprojektleitung und Steuerung der Umsetzung der Renovation unseres Biotechnikums  - Steuerung des Lieferanten, der mit der operativen Umsetzung beauftragt ist - Kosten- und Umsetzungskontrolle ? Koordination mit weiteren operativen Einheiten auf dem Werksgeländes - Weitere kleinere Projekte nach Bedarf - Verantwortung für Budget, Zeitplan, Beschaffung, Qualität und Risiko für dieses Projekt, einschließlich Detailplanung, Ausschreibung, Bau, Abnahme, Fertigstellung und übergabe an das operative team vor Ort - Verantwortlich für Einhaltung der Sicherheitsstandards, Engineering guidelines und GMP Anforderungen ? - Verfolgt und kontrolliert den Fortschritt des Projektes anhand von Zielen, genehmigten Budgets und genehmigten Zeitplänen. - Verantwortlich für turn-over-package und Übergabe an die operativen Einheiten vor Ort   Qualifikationen: - Bachelors oder Masters Degree in Mechanical Engineering oder ähnliches Studium - Mehrjährige Erfahrung in der pharmazeutischen Industrie (GMP) notwendig - ausgewiesener Erfahrung im Projektmanagement sowie spezialisierten Kenntnissen in: GMP Umfeld / Reinraumtechnik, Elektrischer Energieversorgung, Dampferzeugung, GIS-Mittelspannungsanlagen, Heizung und Warmwasser-Erzeugung - Interdisziplinäres Arbeiten - Deutsch und Englisch auf Niveau C1/C2

At nemensis ag, we connected thousands of applicants with their dream jobs and gave them the opportunity to develop or re-enter the job market. For our client, an international pharmaceutical company in Basel, we are in search for a QA / QC-Specialist (f/m/d).   Position purpose: Initiation and supervision of qualification processes of complex analytical systems including the corresponding software qualification. Responsible for the high quality / data integrity of qualification processes, SME-in the related fields. Participator/leader of global harmonized continuous improvement projects. Writing and reviewing of relevant SOPs in compliance with given guidelines.   Responsibilities: - Initiate, support and supervise qualifications of complex analytical equipment (in- cluding corresponding software qualification) in close collaboration with the analytical laboratories - First point of contact to Quality Compliance in all topics related to your field of work - Actively participate in global teams, projects, networks and/or platforms - Interact with authorities / inspectors where appropriate. Act as SME regarding system qualification topics - Manage deviations related to complex analytical systems - Write and review quality documents related to your field of work to ensure compliance to global guidelines   Qualifications: - Technical expert studies with PhD and 0-2 years relevant experience or - Master of Science with 4 years of relevant experience or - Bachelor of Science or equivalent technical education with 8 years relevant experience in industry or equivalent - Fluent in English (oral and written) Basic skills in local site-language (German), as - required for the position & Awareness of safety regulations and for safe - handling of chemicals and equipment. - Appropriate number of years of experience in an analytical GMP environment. - Very good knowledge of qualification processes for laboratory systems in a GMP environment including software qualification (CSV) and related technical tools and software. - Very good with laboratory and/or technical tools. Ability to work in and lead teams.   At nemensis ag you are always welcome with your personality, your ambitions and your professional experience. Share your expertise with us and apply now!

Bei nemensis ag haben wir Tausende von Bewerbern mir ihren Traumstellen in Verbindung gebracht und ihnen die Möglichkeit der Weiterentwicklung oder des Wiedereinstiegs ermöglicht. Wir suchen einen Spezialisten Arbeitssicherheit im Chemieumfeld (m/w/d) 100% für eine feste Anstellung. Das in der Region Zürich ansässige Schweizer Familien-Unternehmen ist ein leistungsstarker Spezialanbieter in seiner Branche, welches international tätig ist.   Ihre Vorteile: Bei unseren Mandanten: - Festanstellung - 6 Wochen Ferien - Selbstverantwortungsvolles Arbeiten - Abwechslungsreiche Tätigkeiten   Was Sie machen werden: - Sie unterstützen die verschiedenen Abteilungen fachlich im Bereich Arbeitssicherheit & Gesundheitsschutz - Dazu gehören auch das Erstellen und Durchführen von Schulungen sowie die Kontrolle für die Einhaltung - Im Bereich Risikoanalysen und Gefährdungsbeurteilungen arbeiten Sie mit den Fachabteilungen zusammen - Das Erstellen von Statistiken, Berichten und Analysen gehört ebenfalls zu Ihrem neuen Aufgabengebiet. Die daraus abgeleiteten Optimierungen setzen Sie mit den entsprechenden Fachbereichen um  Schlüsselqualifikationen: - Abgeschlossene Ausbildung als Chemie-/Pharmatechnologe oder Chemielaborant (w/m) - Erfahrung in einer ähnlichen Funktion im Bereich Chemie / Spezialitätenchemie  - Abgeschlossene Weiterbildung im Bereich Arbeitssicherheit und Gesundheitsschutz - Teamplayer mit hoher Eigeninitiative, konstruktiver Feedbackkultur und offener Kommunikation - Lösungsorientierte und organisierte Persönlichkeit mit ausgeprägtem Sicherheitsbewusstsein - Fliessendes Deutsch in Wort und Schrift sowie Verhandlungssicheres Englisch setzen wir voraus, Französischkenntnisse sind von Vorteil   Wir freuen uns auf Ihre Bewerbung! Bei der nemensis ag sind Sie mit Ihrer Persönlichkeit, Ihren Bestrebungen und Berufserfahrung immer herzlich willkommen. Zeigen Sie uns Ihre Expertise und bewerben Sie sich noch jetzt. Mirjam Hachen, mirjam.hachen@nemensis.com

At nemensis ag, we connected thousands of applicants with their dream jobs and gave them the opportunity to develop or re-enter the job market. For our client, an international pharmaceutical company in Basel, we are in search for a Formulator Specialist (f/m/d).   Position purpose:Job purpose is to plan, perform, optimize and document routine scientific experiments for the preparation and timely delivery of drug products incl. GMP manufacturing. Participate in scientific teams and contribute to the overall Technical Research and Development strategies and goals.   Responsibilities: - Developing formulations of capsules, film coated tablets or sachets, to develop manufacturing processes including scale-up and to manufacture clinical supplies under a GMP environment. - Your responsibilities will be to plan, perform scientific experiments (or pilot plant processes) under minimal guidance from more experienced team members and to contribute to the interpretation and report results. - Plan, organize, perform and document scientific experiments/plant activities in collaboration with experienced team members if necessary. - Seeks proactively for support and coaching from Project Leader, Scientific Expert or other team members during the whole process if necessary - Adherence to quality, quantity, and timelines for all assigned tasks. - Adherence to company's standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards. - Reproducibility of experiments and results. - Refer to annual individual and team objective setting   Qualifications: - Scientific education e.g. BSc or a College of Applied Science Diploma - Experience in manufacturing under GMP - Ideally a minimum of 3 to 5 successful years of experience - Fluent in English, German and/or French is an advantage - Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment - Good scientific or technical knowledge in galenics/ formulation at lab, pilot and production - Adequate knowledge in scientific/technical areas of collaboration - Proficient with laboratory and/or technical tools - Adequate knowledge of software and computer tools - Basic presentation skills and scientific/technical writing skills   At nemensis ag you are always welcome with your personality, your ambitions and your professional experience. Share your expertise with us and apply now!

At nemensis ag, we connected thousands of applicants with their dream jobs and gave them the opportunity to develop or re-enter the job market. For our client, an international pharmaceutical company in Basel, we are in search for an Senior Data Engineer (m/w/d) 100%.   Job Purpose: Senior Data Engineer has the responsibility to design data pipeline architecture in a strong partnership with Product owner to fit with product roadmap needs.He plays a role as a mentor for the Data Engineer community to ensure that best practices and processes are met.Responsible for expanding and optimizing our data and data pipeline architecture, as well as optimizing data flow and transformations.   Responsibilities: - Responsible for defining how to develop the pipeline and his overall quality - Help the team in building new and relevant data engineer features for enhancing the pipeline according to the roadmap. - Plays a mentorship role to ensure the optimal application of best practices, coding conventions over the pipeline and assist data engineer in their duties upon request - Helps the team to achieve and surpass product and program goals - Provides technical guidance and direction as well as contributing hands-on to pipeline development - Acts as an evangelist and guiding practitioner of agile and devops practices   Qualifications: - Bachelor's/Master's degree in Computer Science, Applied Mathematics, Engineering, or any other technology related field; equivalent of the same in working experience may also be accepted - Responsible for expanding and optimizing our data and data pipeline architecture, as well as optimizing data flow and transformations - Strong troubleshooting and problem solving skills - Experience building large-scale software systems and implementation of creative solutions to difficult computational problems (with emphasis on performance and near real-time data analytics) - Senior level data engineering (e.g. ETL) experience - Databricks or Spark experience - Proficient in Python, R or Scala - Experience with AWS / Azure cloud technologies and stack - Experience building big data applications and pipelines using Spark - Strong knowledge in DevOps, coding conventions and best practices for User Acceptance Test   Of advantage: - Experience in medical imaging solutions - Understanding of data42 data capabilities and tools - Understanding of images storage best practices - Technical ability to configure images systems to load and transfer files - Knowledge of medical image formats and metadata - Work closely with data scientists to solve technical issues in building analytical blueprints in ML, DL, and genomic sequence analysis - Understanding of ML/DL and imaging processing in big data computing engine (e.g. Spark) - Familiarity with performance tuning skills (Spark, Data I/O); good knowledge about the internals of Spark and other components in Hadoop ecosystem (HDFS, Hive) At nemensis ag you are always welcome with your personality, your ambitions and your professional experience. Share your expertise with us and apply now.