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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 Principal Biostatistician (f/m/d).   Job Description:As expert, you are supporting the release and stability strategy, the method validation and method transfer activities for our products covering development activities.You will support the operational aspects of GMP testing of Biologics clinical drug substances (DS) and drug products (DP). You independently manage your activities and provide required documentation according to agreed timelines and standards.Your responsibilities: - Responsible for the successful delivery of work packages to support GMP testing of Biologics clinical drug substances (DS) and drug products (DP) for release/stability/validation/transfer - Author and/or review of technical source documents in accordance with project timelines for global submissions. - Review high-quality CMC documentation for HA submission. Your profile: - Well-developed planning, organizational, problem solving and interpersonal skills. - Good communication skills with a collaborative and patient-focused mindset - Computer/IT systems literacy - Education Minimum: Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent; advanced degree desired. - Minimum 2 years of Quality Control experience in a GMP environment and/or pharmaceutical industry experience. - Sound technical and scientific knowledge of pharmaceutical development and analytical sciences. - Knowledge on health authority regulations. - Proven ability to critically evaluate data from a broad range of scientific disciplines. - Proficient in English (other languages are a plus).

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 Aviation Ground Handler (f/m/d).   The role offers an opportunity to be responsible for ground movements and servicing of Japat and tenant aircraft, as well as exterior cleaning of aircraft when required. In addition, you will assist the maintenance department as required and assist the hangar facility manager in keeping the Japat facility clean and tidy.   Your responsibilities: - Marshalling of aircraft on the ramp as well as towing Japat and tenant aircraft from the hangar to the ramp and vice versa. - Welcome and guide Japat and tenant passengers to and from the aircraft prior to departure and after arrival. - Load and unload customer bags to/from the aircraft baggage compartment. - Service aircraft in accordance with the handling approval/manual. - Operate ground service equipment including motor vehicles and tugs. - Clean aircraft exterior and interior. - Support facility services to maintain a tidy hangar, offices and hangar surroundings. - Assist maintenance and aircraft crews in general tasks not requiring certification. - Liaison with third party providers for receiving and sending goods or services.   Your profile: - Real- or Sekundarschool diploma English (required), German (preferred), French (preferred) - Aviation experience preferred - Experience in ramp operations preferred - Car driver license   We look forward to receiving your application! For further questions please contact: Nicolas Gerster, +41 61 205 98 69, nicolas.gerster@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 an Associate Scientist (f/m/d).   Job Purpose:We are looking for a motivated associate scientist to perform physical/chemical testing for Quality Control of development biotech drug substances (DS) and drug products (DP) in collaboration with members of the own and cross-functional teams in a cGMP environment.   Your responsibilities: - Perform and document of physical/chemical experiments (including pH, HPLC or Capillary Electrophoresis, UV) in a cGMP environment. - Address simple problem. Recognize and communicate complex problems. - Inform and support on deviations and unexpected results. - Archive batch records.   Your profile: - Master of Science or Bachelor of Science or Apprenticeship in industry (or equivalent technical education) with 1 year relevant experience in industry. - Minimum of 2 years Quality Control experience in a GMP environment. - Good organization and good communication is a must. - Good technical knowledge in analytical separation. - Adequate knowledge of software and computer tools. - Good understanding of English (oral and written) is essential. German is a plus.   We look forward to receiving your application! For further questions please contact: Annika Schelp, +41 61 205 98 78, annika.schelp@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 aus der Region Luzern suchen wir einen Data Reviewer/Engineer Microbiology (w/m/d).   Ihr Aufgabenbereich: - Review von papierbasierten Rohdaten und Rohdaten innerhalb elektronischer Datenmanagementsystemen - Auslösen, bearbeiten und abschliessen von Abweichungen im Bereich Mikrobiologie - Zusätzliche Aufgaben gemäss Erfahrung   Ihr Profil: - Bachelor oder Master in Mikrobiologie oder einem verwandten Fachgebiet - Erfahrung im GMP‐Umfeld - Gute Deutsch‐ und Englischkenntnisse - MS Office‐Anwenderkenntnisse - Teamorientierte und offene Persönlichkeit   Wir freuen uns auf Ihre Bewerbung! Bei weiteren Fragen kontaktieren Sie bitte: Annika Schelp, +41 61 205 98 78, annika.schelp@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 Senior Expert Engineering.   Job DescriptionFor our ambitious drug delivery device programs reflecting our current and future portfolio needs we are seeking a talented engineer for the development and LCM of medical devices.Your Responsibilities: - Support the technical development and life cycle management of safe and user-friendly (connected) autoinjector and on body pump systems as Senior Expert Engineering. - Translate user and business needs into system/sub-system requirements using the systems engineering tool for requirement and test management. - Define interface specification definition with drug, packaging, label & eco system. - Manage project specific 3rd party activities and support the delivery technology lead. - Work within and contribute to broader cross‐functional drug product development teams. Minimum requirementsWhat you'll bring to the role: - MSc/MA in mechanical/electronics or micro systems engineering or relevant field - Excellent understanding of the current drug delivery technologies. - Autonomous and independent working style with at least 3 years of experience in Medical Device development and LCM. - Ability to interact with cross functional team in matrix organization. - Strong communication skills, emotional intelligence as well as ability to navigate into complex organization and create networks. - Design change management experience and enthusiasm to support the maintenance of existing and building of new platforms. - Proficient spoken communication and excellent technical writing skills in English. - 2 days home office / 3days should be on site!

nemensis is your specialized life sciences recruitment agency based in Basel. Since 2007 we have been matching talent with promising opportunities within the Pharma, Chemistry, BioTech & MedTech industries. We are passionate about connecting people and take pride in finding the right match for our candidates and partner companies. We love that our job revolves around people and the human factor drives us in our daily work. Ready for your next step in YOUR career? We look forward to hearing from you!   For one of our clients, a globally active chemical company, we are looking for a highly qualified   Project Manager, 100% (m/f/d), with an interest in Process Plants      Your scope includes, but is not limited to:  - Having full responsibility for the execution of equipment and system projects within a given budget and timeline - Monitoring your projects regarding schedule, quality, financials and assuraning contract fulfillment - Supporting the sales entities from inquiry through offer and until completion of the negotiation phase - Coordinating, liaising and managing claims of both customers and suppliers - Cooperating with and coordinating internal stakeholders - Supervising start-up, commissioning and performance tests on-site   The following qualifications and experience will help you succeed in this role: - You have a technical degree or education - You are Project Management certified (e.g. Scrum, PMP, IPMA) - You are experienced with complex project work, preferably in the process industry, and are familiar with external/end-client contact  - You have at least 5 years of experience as a Project Manager in an international environment - You follow a structured process and have strong problem-solving skills - You are able to work independently, have a strong customer focus and demonstrate solid negotiation skills - You are a skilled communicator and stakeholder management, across various levels of hierarchy - You are fluent in verbal and written English. German would be highly advantageous and any further languages will be an asset     What the Company has to offer   You will be receiving attractive compensation as well as excellent social benefits. You will become part of an innovative, vibrant, and agile culture. Thanks to the global reach of the company, your development opportunities and possibilities for mobility are international. The company is located close to Basel, is easily accessible with public transporation (bus/tram), and offers free parking space for those travelling by car.    I look forward to receiving your applications through our platform and am happy to answer your questions at tania.menzi@nemensis.com or +41 79 476 70 13. Please note that applications via Email will NOT be considered. 

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 aus der Region Luzern suchen wir einen Analytical Chemist (w/m/d).   Ihr Aufgabenbereich: - Selbständige Durchführung aller administrativen und analytischen Aktivitäten im Labor - Entwicklung, Validierung und Durchführung von Methoden für die Freigabe und Stabilität von Fertigprodukten (auf Polymerbasis) - Analytische Techniken: vor allem HPLC/UPLC, Dissolution, automatisiertes Equipment - Dokumentation von Ergebnissen in deutscher und englischer Sprache - Ausführung und Überprüfung von Kalibrierungen und Unterhaltsarbeiten an analytischen Geräten, evtl Unterstützung der Gerätequalifizierung - Zusammenarbeit mit (Projekt)managern, Technikern und externen Dienstleistern - Bearbeitung von Abweichungen - Erstellung von Standard Operating Procedures (SOPs)   Ihr Profil: - Bachelor Abschluss (Fachbereich Chemie oder vergleichbar) oder abgeschlossene Ausbildung als Laborant mit mehrjähriger Berufserfahrung, weiterer Master Abschluss von Vorteil. - Erfahrung mit chromatographischen Analysenmethoden (HPLC), Freisetzungs-Assays (Dissolution/HPLC) und GMP-Richtlinien. - Sehr gute Englischkenntnisse (in Wort und Schrift). - Hohe Affinität zu komplexen EDV Systemen und komplexer Labortechnik (zB. Labor Automatisierung). - hohes Qualitätsbewusstsein und Sinn für eine effiziente Arbeitsweise. - ausgeprägte Fähigkeit zur Lösung komplexer Probleme und Fragestellungen im Team aber auch in selbstständiger Arbeitsweise. - ausgeprägte Lernbereitschaft und Selbständigkeit. - teamorientierte und offene Persönlichkeit.   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 Formulation Manufacturing Project Leader.   Position purposeJob purpose to support drug product manufacturing process related development and supply activities for parenteral and ocular small molecule drug products in Post POC phase. This includes the scientific evaluation and presentation of data, authoring of technical and GMP documentation, integrity checks against raw data and on-site manufacturing support to technical and clinical manufacturing campaigns. You work in a cross-functional team with manufacturing operations, analytics and QA and contribute to the overall Technical Research and Development strategies and goals. You work under minimal guidance of more experienced formulation project leaders. Your responsibilities: - support drug product formulation development and manufacturing activities at internal or external manufacturing sites for assigned projects in line with the project plan, guidelines and procedures - collaborate with operational colleagues working on your process at the respective manufacturing sites - take accountability for formulation and manufacturing process deliverables incl. GMP related aspects and change control - author manufacturing instructions for clinical manufacturing campaigns, compile data and interpret results, evaluate data, draw relevant conclusions and contribute to development reports and Quality risk assessment documents in close collaboration with the project teams - perform document reviews and data integrity checks against raw data - support deviation investigations and drive change control - exchange regularly within your project team as well as seek guidance with internal experts on diverse aspects   Your profile: - Master degree or higher in life sciences, ideally in the Pharmaceutical field - Ideally more than 5 years industrial experience in the development and / or clinical manufacturing of pharmaceutical formulations for small molecules and with experience in late phase development and launch activities. Experience in ocular or parenteral development preferable. - Interdisciplinary thinking and interest in collaboration with other functions - Good knowledge of GMP and GLP - Good knowledge of ocular and/or parenteral dosage form technologies and laboratory and/or technical tools - Good scientific / technical writing skills - Fluent in English (oral and written), German is an advantage.

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 Senior Scientist.     This is an exciting opportunity to join the Molecular & Cellular Sciences (MCS) team within Biomarker Development (BMD) and Translational Medicine (TM) at the Institutes for Biomedical Research (NIBR). BMD focuses on delivering fit for purpose integrated biomarkers leveraging diverse expertise and knowledge in immunology, genomics, protein and cellular biology and state of the art data sciences.Our innovative spirit enables the development and application of cutting-edge technologies which address key clinical questions such as target engagement, defining disease stage or progression, predict the safety or efficacy of medication, select a group of patients who would benefit most from a given therapy, and identify additional clinical indications suitable for a innovative molecule.As a Senior Scientist within MCS in BMD, you will work in close collaboration with project and clinical teams to develop novel exploratory assays in our state of the art laboratories, implement internal and external biomarker activities and interpret results to enable proof of mechanism, proof of biology, safety and efficacy understanding. As a soluble biomarker assay expert, you will be developing and validating innovative biomarker solutions implementing new methodologies, delivering high quality data and playing a pivotal role in human clinical trials.Your responsibilities:? Development and validation of soluble biomarker assays with special focus on ligand binding assays (ELISA, MSD, Luminex) and other state of the art technologies.? Implementation (sample measurement and data transfer) of validated biomarker assays in clinical studies.? Generate and interpret data to enable proof of mechanism, dose selection & proof of biology across early clinical programs and present results at internal meetings? Providing subject matter expertise to transition, implement and monitor assay development and validation at CROs? Ensuring quality and timely delivery of data generated through outsourced activities? Empowered for experimental design, execution, interpretation and reporting (oral and written) of assigned projects under Unboss culture.? Contributing to write quality reports and laboratory manuals.? Cross training on a variety of biomarker modalities and technologies? Develop and validate fit-for-purpose soluble biomarker solutions? Independently design, execute, and interpret experiments? Ensure high quality and timely delivery of internal and external results? Providing subject matter expertise for transferring, implementation and monitoring of soluble biomarker assay development, validation and sample analysis at external providerYour profile:? BS/MS degree in Biology, Immunology, Cell biology or equivalent with wide experience as a laboratory technician with 5+ year in the pharmaceutical or biotechnology environment? Extensive understanding, knowledge and practical experience in ligand binding assays are essential, and experience on Mass spectrometry and other related technologies will be a plus.? Analytical thinking, willingness to accept responsibility, and teamwork skills? Experience working in a global organization and matrix-resourcing model? Good Computer skills (Excel, Word, PowerPoint, Soft MaxPro, SMART Book, GraphPad Prism, Watson LIMS)? Good communication skills for oral and written in English? Understanding of regulatory requirement relevant to Biomarker Development (e.g. GCLP, ICH)

Heizwerkführer/Kesselwärter 100% per sofort 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 Heizwerführer/Kesselwärter 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 - Finanzielle Unterstützung bei Weiterbildungen/Temptraining Bei unseren Mandanten: - Grosses, internationales Unternehmen - Chance auf eine Festanstellung - Unternehmen mit sehr guter Reputation - Selbstverantwortungsvolles Arbeiten - 40h/Woche - Chancengleichheit - Weiterbildungsmöglichkeiten Sie erwarten folgende spannenden Aufgaben: - Sicherstellen des Betriebes der zugeteilten Anlagen (Rauchgasreinigung, Abluft- und Abgasentsorgung, Dampfturbinen, Hochtemperaturofen, etc.) - Bedienung von PLS und direkte Handeingriffe an der Anlage - Protokollierung der ausgeführten Arbeiten und Auswertung der Monitoringdaten - Allgemeine Unterhalts- und Reinigungsarbeiten - Arbeiten im Schichtbetrieb -   Für diese Tätigkeit bringen Sie folgende Qualifikationen mit:  - Abgeschlossene Ausbildung als Chemikant/in, Schlosser/in, Mechaniker/in, Werkzeugmacher/in, Metallbauer/in, etc. - Weiterausbildung mit Diplom zum Kesselwärter oder Heizwerkführer mit eidg. Fachausweis von grossem Vorteil - Erfahrung in der Bedienung und Überwachung von komplexen Anlagen, Verbrennungsanlagen von Vorteil - Bereitschaft für Schichtdienst - Verantwortungsbewusste, kommunikative und belastbare Persönlichkeit    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