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 company in Schachen, we are in search for a Scientist (f/m/d). Employment type: Temporary via nemensis ag, 100% Duration: 01.06.2022 - 31.12.2022, Backfill Maternity Leave Weekend readiness: yes Salary: CHF 35 - 42.- / h gross Your responsibilities: - Perform in-process analytics independently according to guidelines. - Calibration and maintenance of equipment. - Perform Batch and Continuous Fermentation and Harvest processes according to Batch Sheet or superior's demand in pilot scale. - Follow company policies and works according the internal and external safety, health, and environment guidelines. - Documention of all performed works according to GDP. Your Profile: - Apprenticeship as a Laboratory Technician (or similar). - GMP practical experience or Candidates with a theoretical GMP training and practical fermentation experience in the pharmaceutical, food or chemical industries. - Language skills in English and German at least at B1 level in written and spoken. - Knowledge about cGMP rules and the observance of them in the area of responsibility. We look forward to receiving your application! For further questions please contact: Kristina Mutidi +41 61 205 98 77 kristina.mutidi@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 company in Basel, we are in search for an Associate Scientist (f/m/d). Employment type: Temporary via nemensis ag, 100% Work location: Basel, onsite only Duration: asap - 31.03.2023 Salary: CHF 36 - 40.- / h gross Job Purpose:The global Pharmaceutical Intelligence (PharmINT) & Forensics strategy is fully embedded in the company's Combatting Falsified Medicines program, which is destined to combat pharmaceutical crime and create the conditions to bring counterfeiters and illegal traders to justice, recover losses through legal action, improve patient safety, preserve the company's reputation and create a tangible return on investment for the business. The Anti-Falsified Medicines, Scientist, PharmINT & Forensics is a specific and technical role, reporting the Anti-Falsified Medicines, Director, PharmINT & Forensics at Global Security. The Anti-Falsified Medicines, Scientist, PharmINT & Forensics will work to advance the state-of-the-art analytical techniques to primary gather spectrometric data to feed the spectra libraries of Nthe company's genuine. Initially, he/she will be contributing to the management of the life cycle and the chain of custody of falsified medicines exhibits and the execution genuine Drug Substances and Drug Products collection to support the spectral libraries development and perform phamactial process operations in solid oral technicum. He/she will work closely with PharmINT& Fo-rensics team to deliver the timely delivery to deliver spectra for methods development and maintenance to empower the authentication services.This position will require close collaboration and substantial interaction with Global Security Associates as well as various internal stakeholders (i.e. manufacturing sites, Technical Research & Development, Quality). Your responsibilities: - Meet quality, quantity and timelines in all assigned Anti-counterfeiting operations, networks and/or PharmINT & Forensics services: Work on assigned priorities and to an agreed plan, through the systematic collection, spectroscopic data gathering according to appropriate SOPs, GMP, GLP, QM, HSE, and ISEC and the company's guidelines into timely accurate and relevant Phar-mINT deliverables. - Collaborate with appropriate technical resources and experts to develop new use cases for Authentifield bythe company: Quantification, Container wise testing and Real-Time-Release testing. - Support or perform/execute operations related to the development, validation, transfer and maintenance of accurate and traceable cross-divisional spectral libraries to support the development of robust multivariate/Chemometrics statistical methods for reliable, cost efficient and realtime detection of counterfeit medicines: - Plan and manage the collection of genuine drug products covering the manufacturing (i.e., Sites and Variants) - Plan and manage the development, validation, transfer and maintenance of the spectral library. - Collect spectra of genuine samples using vibrational spectrometric techniques as per the library development plan - Develop and maintain excellent working and reciprocal relationships with internal associates from other functions to facilitate transfer of knowledge and deliveries of Drug Substances and Drug Products. Your profile: - Chemical or pharmaceutical scientist (with bachelor or MSc in Life Sciences, forensics, Pharmacy or Medicines from accredited Technical University) or equivalent education with experience in pharmaceutical industry. - 1-3 years' experience undertaking similar roles in the Pharmaceutical Industry with a particular focus on analytical and forensic sciences as well as pharmaceutical technology and quality Control. Operational experience should include manufacturing, forensic, QA/QC management, development or other relevant experience e.g. working at a regulatory health authority and/or law enforcement. - Excellent knowledge of laboratory and/or technical tools. - Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities e.g., spectrometers, handheld devices labs. - Good scientific and technical knowledge in analytical chemistry and galenical development. - Proficient in computational analysis of field measurement data with Python with data management and integration skills is a plus. - Experience working in a matrix environment with global, cross-functionally teams. - Quick learner, problem solver, working flexibly and in autonomy with solid written and verbal communication skills. - Languages: Fluent in English We look forward to receiving your application! For further questions please contact: Nicolas Gerster, +41 61 205 98 69, nicolas.gerster@nemensis.com
Per azienda cliente settore elettronico selezioniamo TECNICO DI SVILUPPO PRODOTTO Mansioni - Sviluppo e Ingegnerizzazione di nuovi prodotti (Sensori di Pressione, Circuiti Ibridi, Circuiti Elettronici) - Definizione delle specifiche e ciclo di lavoro di un nuovo prodotto - Gestione avanzamento campionature e prototipi in funzione delle tempistiche concordate - Identificazione di materiali, componenti e di attrezzature idonee allo sviluppo e alla realizzazione di nuovi prodotti e relativa gestione dei fornitori - Gestione relazione diretta con clienti per definire e/o discutere le specifiche tecniche dei prodotti in sviluppo Requisiti - Laurea in Fisica, Ingegneria Chimica o Ingegneria dei Materiali - Conoscenza di : processi di Chip & Wire, SMT, serigrafia di circuiti - Pregressa esperienza nella progettazione di prodotti di microelettronica
Bei der nemensis ag haben wir bereits tausende Bewerber mit ihrem Traumjob verbunden und ihnen die Möglichkeit gegeben, sich weiterzuentwickeln oder wieder in den Arbeitsmarkt einzusteigen. Für unseren Kunden, ein internationales Unternehmen im Raum Stein suchen wir einen QC Analysten (m/w/d). Vertragsart: Temporär über nemensis ag, 100% Beschäftigungsdauer: 01.06.2022 - 30.11.2023 Schichtarbeit: keine Schichtarbeit Home Office: nicht möglich Lohnspanne: CHF 36 - 40.- / Std. brutto Ihre Rolle: Als QC Analyst führen Sie die zugewiesenen Aufgaben im Qualitätskontrolllabor in Übereinstimmung mit den cGxP-Vorschriften. Sie führen laborspezifische Tätigkeiten wie Analysen, Wartung, Kalibrierung und Qualifizierung von Analysegeräten aus. Ihre Aufgaben: - Analytische Prüfung und Dokumentation von API-, Wirkstoff-, Arzneimittel-, Fertigprodukt-, Beanstandungs-, Stabilitäts- und Verpackungsmaterialproben. - Betriebliche Probenlagerung und -verwaltung. - Prüfung der Proben - Sicherstellung aller Aktivitäten in Übereinstimmung mit cGxP, einschließlich Datenintegrität. - Analytische Dokumentation von Stabilitätsproben nach cGxP-Standards. - Einhaltung aller HSE-Richtlinien. - Erkennen und melden potenzieller Unfälle und Risiken und Vorschlagen von Lösungen. - Verantwortlich für die Teilnahme an Erstschulungen und Umschulungen. Ihr Profil: - Abgeschlossene Lehre als Laborant/in oder gleichwertige Ausbildung - Frühere Erfahrungen in einer Laborumgebung in der pharmazeutischen Industrie (Qualitätssicherung, Produktion) - Fliessende Deutschkentnisse - Grundkenntnisse in Englisch Wir freuen uns auf Ihre Bewerbung! Bei weiteren Fragen kontaktieren Sie bitte: Kristina Mutidi kristina.mutidi@nemensis.com Tel.: +41 61 205 98 77
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 an Expert Science & Technology, Formulator Specialist, Oral Dosage Forms. Employment type: Temporary via nemensis ag, 100% Duration: asap - 15.12.2022 Salary: CHF 41 - 45.- / h gross Your role: The purpose of this role is to develop our growing pipeline of oral products. We are looking for an expert in the area of Oral Solid Dosage Forms (small molecules, NCE). As a member of the team, you will play a key role in the development of formulations and processes for oral dosage forms with end-to-end scope, from first-in-human trials to marketing phase. You will plan, perform and document scientific experiments for formulation- and process development for preparation and timely delivery of drug products incl. support at GMP manufacturing, primarily in the area of Oral Solid Dosage forms. You will participate in scientific teams and contribute to the overall Technical Research and Development strategies and goals. Your accountabilities: Your duties will be to develop formulations of capsules, film coated tablets or sachets, to develop manufacturing processes including scale-up. In addition you will support the process transfer to GMP Pilot Plant, and support the manufacture of clinical supplies under a GMP environment. Your responsibilities will be to plan, perform scientific experiments (or pilot plant processes) for formulation- and process development under minimal guidance from team members and to contribute to the interpretation and report results. You have experience in using digital tools e.g. for reporting of experiments, and are curious to utilize and to further advance data&digital tools. - Plan, coordinate, perform and document scientific experiments in collaboration with functional and project leads - Develop phase appropriate formulations for oral drug products - Develop efficient and robust processes for oral drug products - Provide raw data documentation, evaluation and interpretation of results - Propose and provide input for the design of next experiments - Transfer procedures/instructions to GMP production facilities (e.g. Pilot Plant, NTO), including troubleshooting - Support the manufacture of clinical supplies under a GMP environment - Contribute to maintenance of infrastructure/equipment. - Adherence to quality, quantity, and timelines for all assigned tasks. - Reproducibility of experiments and results. Your profile: - Degree in Pharmaceutical Sciences or a related discipline (e.g. BSc with 2 years industry experience or a College of Applied Science Diploma or equivalent, lab technician with 3 years industry experience and relevant on the job training). - Experience in manufacturing under GMP is advantageous Experience. - Minimum of 3-5 years of experience in pharmaceutical development of oral solid dosage forms, e.g. in lab, technicum or Pilot Plant setting, with experience in the most common pharmaceutical technologies und unit operations. - Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment. - Good scientific or technical knowledge in galenics/pharmaceutical technology / formulation- and/or process development at lab, pilot and production. - Excellent user experience of software and computer tools (e.g. electronic documentation). - Proficient with laboratory and/or technical tools. - Excellent organizational skills with respect to planning, tracking, priority setting and adherence to project timelines - Proficiency in English required (oral & written), German and/or French is a plus. We look forward to receiving your application! For further questions please contact: Nicolas Gerster, +41 61 205 98 69, nicolas.gerster@nemensis.com
Bei der nemensis ag haben wir bereits tausende Bewerber mit ihrem Traumjob verbunden und ihnen die Möglichkeit gegeben, sich weiterzuentwickeln oder wieder in den Arbeitsmarkt einzusteigen. Für unseren Kunden, ein internationales Unternehmen, suchen wir einen Senior Laborant für die Analytik. Ihr Aufgabenbereich: - Entwickeln, Optimieren und Troubleshooting von chromatographischen Methoden (HPLC, UPLC, GC, GCH) mit Hilfe des modernen Geräteparks - Implementieren, Validieren und Transferieren von chromatographischen/massenspektrometrischen Analysemethoden an einem modernen Arbeitsplatz - Qualifizierung und Betreuung des analytischen Geräteparks - Aktive Mitarbeit an spannenden analytischen Projekten von der frühen Entwicklungsphase bis hin zur Prozessreife - GMP-konformes analysieren pharmazeutischer Wirksubstanzen und Stabilitätsstudien Ihr Profil: - Ausbildung als Chemielaborant/in EFZ, Bachelor in Life Science Oder vergleichbare Ausbildung mit Schwerpunkt Analytik - Berufserfahrung in einer ähnlichen Funktion sowie Interesse und Kenntnisse an chromatographischen Trenntechniken - Exakte und zuverlassige Arbeitsweise - Erfahrung im Umgang mit Chromeleon, Empower, LIMS, MS-Office und GMP sind von Vorteil - Sehr gute Deutschkenntnisse in Wort und Schrift
Bei der nemensis ag haben wir bereits tausende Bewerber mit ihrem Traumjob verbunden und ihnen die Möglichkeit gegeben, sich weiterzuentwickeln oder wieder in den Arbeitsmarkt einzusteigen. Für unseren Kunden, ein internationales Unternehmen, suchen wir einen Senior Laborant für MS. Ihr Aufgabenbereich: - Entwickeln, Optimieren und Troubleshooting von LC-MS/GC-MS Methoden und chromatographischen Trennmethoden fur die Analyse von small molecules - Strukturaufklärung mittels LC-MS/GC-MS, sowie Interpretation von Analyseergebnissen - Implementieren, Validieren und Transferieren von chromatographischen/massenspektrometrischen Analysemethoden an einem modernen Arbeitsplatz - Qualifizierung und Betreuung des analytischen Geräteparks - Aktive Mitarbeit an spannenden analytischen Projekten von der frühen Entwicklungsphase bis hin zur Prozessreife - GMP-konformes analysieren pharmazeutischer Wirksubstanzen Ihr Profil: - Ausbildung als Chemielaborant/in EFZ, Bachelor in Life Science Oder vergleichbare Ausbildung mit Schwerpunkt Analytik - Praktische Erfahrung in der Chromatographie und Massenspektrometrie (LC-MS/GC-MS) - Praktische Erfahrung in der chromatographischen/massenspektrometrischen Methodenentwicklung und Troubleshooting - Exakte und zuverlassige Arbeitsweise - Erfahrung im Umgang mit Chromeleon, Masshunter, Empower, LIMS, MS-Office und GMP sind von Vorteil - Sehr gute Deutschkenntnisse in Wort und Schrift
My client is an innovating, dynamic and growing international pharmaceutical company, looking for a Statistical Programmer with a strong experience with SAS programming and CDISC. As the new Statistical Programmer, you will be responsible for leading, developing and implementing statistical solutions to the company R&D sponsored clinical trials. Within this role, you will perform statistical programming activities for all assigned clinical studies sponsored by the company. Job Responsibilities: - Provide statistical programming expertise with respect to Statistical Programming, Biostatistics - Perform/Coordinate all statistical programming related tasks - Support the development of tables, listings and figures for assigned projects - Work closely with statisticians to deliver all the statistical deliverables - Create derived data set specifications for all assigned studies and integrated summaries - Provide oversight and guidance to CRO for all statistical programming related activities, including development and validation of ADaM - Review statistical analysis plans for all assigned studies and integrated summaries and provide comments to study biostatistician - Review annotated case report forms and provide comments - Contribute to process improvement initiatives as assigned Minimum Requirements: - Minimum of 6-7 years of SAS Programming experience including statistical programming experience in pharmaceutical setting - Extensive experience in applying SAS programming language, preferably in pharmaceuticals setting - Very good knowledge of CDISC Standards, including SDTM, ADaM - Master's or bachelor's degree in Statistics, Mathematics, Computer Science, or any related field - Knowledge in SAS macros - Good understanding in statistical methods used in statistical analysis - Ability to review protocol and SAP and provide feedback - Good understanding in Good Programming Practices in pharmaceutical industry - Fundamental knowledge of GCP standards For more information, please feel free to contact Morgane CAYUELA at mc@axepta.com
Mon client, entreprise internationale biopharmaceutique en pleine croissance, recherche un Technicien de laboratoire de Biotechnologie avec votre experience en purification de protéine à l'echelle laboratoire. Ce poste est un CDI basé dans le nord du canton de Vaud. RESPONSABILITÉS : Exécution d'expériences de purification de protéine Participation à la mise en place de nouveaux équipements Préparation de solutions et milieux de culture Expérimentation de purification de protéine et de caractérisation du procédé à petite échelle (chromatographies (Äkta), UF/DF, SPTFF, nanofiltration). Soutien dans l'exécution des études de culture cellulaire Mise en place de méthode d'analyse comme HPLC, TECAN.. Package de colonne de chromatographie à échelle de laboratoire Contribution à l'organisation du laboratoire et des commandes Rédaction des SOPs, protocoles d'études et documents Process Sciences Participation à au commissioning et qualification de nouveaux équipements Respecter les exigences légales et les conformités ainsi que des directives de l'entreprise Collaboration avec les départements partenaires sur le site (QC, MFG, QA) et avec les laboratoires Process Sciences aux Etats-Unis PROFIL : Niveau CFC de technicien de laboratoire 3 ans d'expérience en laboratoire de biotechnologies et en purification de protéines Maitrise des instruments FPLC (AKTA) Connaissance des GLP Capacité à travailler dans un environnement très régulé et qui change très vite Esprit d'équipe Bon niveau d'anglais
Nous recherchons actuellement un Quality System Engineer, pour l'un de nos prestigieux clients, de renommée mondiale et en pleine croissance, spécialisé dans les dispositifs médicaux et basé à Genève. Responsabilités: - La gestion et l'amélioration du SMQ conformément aux normes ISO 13485 et 21 CFR 820 - Le pilotage du processus de gestion des risques via l'ISO 14971 - Veiller au respect du système de suivi des actions correctives, des Change Controls, des analyses de risques... - Participer aux audits internes/externes et suivre la résolution des non-conformités associées - Suivre les KPI Votre profil: - De formation en Life Sciences (Master ou équivalent), vous justifiez nécessairement d'au moins 4 ans d'expérience pour la gestion du SMQ et du processus de gestion des risques dans l'industrie des Dispositifs Médicaux - Maitrise des normes ISO 13485, 21CFR820 applicables aux DM - Expérience de la gestion des risques via l'ISO 14971 - Vous parlez Français et couramment anglais Pour plus d'informations, n'hésitez pas à contacter Morgane CAYUELA mc@axepta.com
We are looking for a Biological Sample Operations Manager in order to coordinate operations and logistics for testing, analysis and storage of biological samples for clinical trials and translational projects, performed by external providers. Join the Clinical Operations Department of one of our prestigious biopharmaceutical clients, based in the canton of Vaud. Responsibilities: - Manage sample tracking, receipt and storage processes for clinical and translational projects - Support clinical study activities in the preparation and review of study related documents - Interface with laboratory personnel, sample processing vendors, and other vendors (e.g., long-term storage vendor) as needed to ensure proper shipment of samples, respond to issues as appropriate, and ensure study objectives are met - Possibly contribute to the assessment of site and laboratory feasibility for the collection, handling and storage of biological samples - Be responsible for the development and maintenance of a biorepository database for human and non-human biological samples. - Ensure consistency of biospecimen process in clinical studies within their respective projects and manage specimen logistics from patient to data in compliance with GXP - Participate in process improvement projects (SOPs, work instructions, training materials) in collaboration with QA and clinical study teams - Forecast operational costs for biopsies and review contracts and invoices Profil: - Background in Life Sciences (Bachelor or Master Degree) - At least 3 years of experience working with biological sample management & coordination in clinical trials - Used to work with Central Laboratory, CRO or different vendors as long term storage vendors - Good understanding of overall Clinical Trial Operations and Translational Medicine - Strong knowledge of GCP, GCLP and ICH guidelines - English fluent, good knowledge of French an asset For more information, please feel free to contact Morgane CAYUELA at mc@axepta.com
My client is an innovating, dynamic and growing international pharmaceutical and healthcare company currently expanding their Global Regulatory Affairs team in Switzerland, Lausanne. Due to this growth my client is looking for a Global Technical Regulatory Affairs Manager with experience working on Cosmetics Products at global level to be part of the projects of development/maintenance; coordinating, preparing and reviewing the global cosmetic dossiers, ensuring the regulatory compliance of the Raw Material portfolio, the Packaging and the dossier sections related to manufacturing sites. Responsibilities: - Ensures compliance with relevant worldwide regulations from a technical standpoint (notably regulation EU 1223/2009/EC, REACH 1907/2006, STSC, CFR...). - Technical focal point of contact for manufacturing sites, procurement, supply chain, quality, safety and formulation teams. - Represents technical RA in global & cross functional meetings - Communicates of project relevant RA information to Project Team and Department Heads - Cooperates with RA Franchises in setting up the regulatory strategy for projects (development and LCM) - Performs the gap and impact analyses of changes. - Maintains and track RA activities databases - Ensures right processes and structures are in place for cosmetics and other topical products. - Participates to regulatory watch for ingredients, technical FP topics and technical parts of country regulations. - Prepares and participates to meetings with Health Authorities if necessary Your profile: - Minimum 2-5 years of experience in global Regulatory Affairs in the Consumer Care environment (cosmetics). - PhD (in Sciences, Medicine or Pharmacy), Master or any equivalent advanced scientific degree in a related technical field - Strong knowledge of the cosmetic industry, including solid knowledge of all associated global RA regulations - Fluent in English.
Bei der nemensis ag haben wir bereits tausende Bewerber mit ihrem Traumjob verbunden und ihnen die Möglichkeit gegeben, sich weiterzuentwickeln oder wieder in den Arbeitsmarkt einzusteigen. Für unseren Kunden, ein internationales Unternehmen in der Region Basel, suchen wir eine/n Chemielaborant/In. Vertragsart: Temporär über nemensis ag, 100% Beschäftigungsdauer: 01/06/2022 - 30/06/2023 Bruttolohn: CHF 37 - 42.- / Std. Ihre Rolle: Selbständige, GMP-konforme und termingerechte Planung, Durchführung, Auswertung und Dokumentation aller zugewiesenen im Labor anfallenden Arbeiten unter Einhaltung der Analysenvorschriften, SOP's und Sicherheitsrichtlinien. Eigenverantwortung für die Prozesse innerhalb der Laborgruppe und Sorgfalt für die zugeteilte Arbeiten und Gerätschaften. Ihre Aufgaben: - Selbständige, termingerechte Planung, Durchführung, Auswertung, Dokumentation und Interpretation komplexer und anspruchsvoller Arbeiten. Löst auftretende Probleme vorwiegend selbst. - Einhaltung von Terminvorgaben z.B. im Rahmen von NOSSCE und rechtzeitige Eskalation im Fall von absehbaren Verzögerungen. - Einhaltung der GMP-, GSU ? Vorschriften. - Pflege, Betrieb und Unterhalt der Geräte und Einrichtungen. - Übernahme komplexer und anspruchsvoller zusätzlicher Aufgaben (z.B. Methodentransfers, Entwicklungsarbeiten, Laboruntersuchungen, Problemlösungen). - Übernahme von Spezialaufgaben mit zusätzlicher Verantwortung (z.B. Poweruser, GSUBeauftragter, Mitarbeit bei der Gerätequalifizierung bei neuen Geräten / Techniken, etc.). - Selbständige Erstellung von Berichten (z.B. Methodenvalidierung, OOS,..). - Einarbeitung neuer Mitarbeiter. Ihr Profil: - Ausbildung als Chemielaborant. - Mindestens 3 Jahre Laborerfahrung (zusätzlich zur Lehrzeit), fundierte Erfahrung in Qualitätskontrolle oder analytischen Labors. - Besitzt vertiefte Kenntnisse in allen gängigen Laborrelevanten Techniken oder alternativ Expertenwissen für Spezialtechniken. - Gute IT-Kenntnisse: Office-Anwendungen, SAP, LIMS. - Fliessende in Deutsch- und Englischkenntnisse. Wir freuen uns auf Ihre Bewerbung! Bei weiteren Fragen kontaktieren Sie bitte: Nicolas Gerster, +41 61 205 98 69, nicolas.gerster@nemensis.com
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 Pharmaceutical Scientist (f/m/d). Employment type: Temporary via nemensis ag, 80-100% Duration: 01/06/2022 to 31/05/2024 with option for extension Remote work: no Salary: CHF 41 - 45.- / h gross Your role: For the development of oral solid dosage forms, we are looking for a scientist with expertise in the area of Oral Dosage Form development and manufacturing for small molecules to support the growing pipeline of products for oral administration. The position is within the Pharmaceutical Development Department (PHAD) within Global Technical R&D. Your responsibilities: - You will work together in a team with other experts and support development and manufacturing activities in the non GMP and GMP manufacturing plants at different manufacturing scales (mainly Lab and Pilot scales). - You will plan and perform scientific experiments for formulation and process development and establish the related lab documentation in electronic documentation systems. - You will as well author manufacturing instructions, contribute to and co-author development reports and Quality Risk Assessments and compile data from manufacturing campaigns and perform the scientific evaluation of process and in-process control data. This also includes document reviews and data integrity checks against source data and the support of investigations. Your profile: - Master's Degree or PhD in Pharmaceutical Sciences or related discipline. - Good scientific knowledge in Pharmaceutical Technology and some experience in formulation and pharmaceutical process development - Work experience in a laboratory environment and you have a good understanding of GMP. - You enjoy working with scientific data and drawing conclusions in scientific reports and you are open to learn new skills in working with electronic documentation systems. - Work experience in the safe handling of Active Pharmaceutical Ingredients (Small molecule Drug Substances). We look forward to receiving your application! For further questions please contact: Nicolas Gerster, +41 61 205 98 69, nicolas.gerster@nemensis.com
Il nostro cliente, realtà in forte espansione del settore Moda, ci ha incaricato di selezionare UN PRODUCT COMPLIANCE & SUSTAINABILITY COORDINATOR da inserire nel team di Supply Chain con sede nel Mendrisiotto. Il/la candidato/a riporterà direttamente al Production Manager e sarà responsabile della conformità e sostenibilità del prodotto e della gestione del processo con i principali partner e stakeholder: Il/la candidato/a inserito si occuperà in particolare delle seguenti attività: ? Supportare la preparazione e la pianificazione di audit e ispezioni. ? Supportare lo sviluppo e l'attuazione della strategia complessiva di sostenibilità e gestione del prodotto ? Coordinare le attività relative alla qualificazione delle materie prime e dei fornitori specificamente legate alla Responsabilità Sociale d'Impresa ? Partecipare all'esecuzione di analisi del rischio di qualità relative a materie prime, prodotti finiti ? Raccogliere e valutare con regolarità i dati KPI idonei a valutare l'efficacia dei Sistemi Qualità in conformità con gli aggiornamenti di leggi e regolamenti per i paesi in cui il marchio è presente. Completano il profilo: ? Conoscenza dei requisiti di qualità nel settore Moda/Fashion e delle leggi e dei regolamenti in materia di sicurezza dei prodotti e requisiti dei test di laboratorio ? Ottima conoscenza del sistema Office in generale e in particolare utilizzo di Ms Excel. ? La capacità di redigere un sistema di reporting ? Pensiero strategico e innovativo con la capacità di valutare le opportunità di mercato sfruttate per fornire azioni di riduzione dei costi e miglioramento del servizio. ? Fluente in inglese e italiano Sede di lavoro: Mendrisiotto Assunzione a tempo indeterminato diretta con il cliente.
