[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-technical-rd-analytical-project-lead":3,"similar-technical-rd-analytical-project-lead":33},{"id":4,"slug":5,"title":6,"skills":7,"budget":18,"duration":19,"location":20,"onsitePercent":18,"contractType":21,"foundAt":22,"category":23,"description":27,"rawText":28,"webTitle":6,"webText":29,"language":30,"projectId":31,"sourceUrl":32},7490,"technical-rd-analytical-project-lead","Technical R&D – Analytical Project Lead",[8,9,10,11,12,13,14,15,16,17],"HPLC","UHPLC","Mass Spectrometry","UV detection","Fluorescence","Analytical Chemistry","Chromatography","Project Management","Regulatory Documentation","English",null,"12+ months","Basel","temp_work","2026-06-02T13:06:41+00:00",{"id":24,"slug":25,"label":26},14,"medical_tech","Medizintechnik","Analytical project lead position in pharmaceutical technical development focusing on synthetic molecules drug substances. Requires expertise in HPLC\u002FUHPLC\u002FMS and analytical method development. Role involves leading analytical control package development and managing external CDMO\u002FCLO activities.","Technical R&D – Analytical Project Lead\n\ntemporary\nTechnical R&D – Analytical Project Lead\nTechnical R&D – Analytical Project Lead: HPLC\u002F UHPLC\u002F MS\u002F UV, Mass Spectrometry \u002F Fluorescence\u002F synthetic molecules drug substances \u002F German\u002F English\nBackground:\nPharma Technical Development (PTD) is a global team of over 2,000 experts focused on developing innovative medicines to address patients‘ needs.\nWithin PTD, Synthetic Molecules Technical Development (PTDC) specializes in drug substance, drug product, and analytical sciences. PTDC is instrumental in advancing the synthetic molecules pipeline, supporting research, early development, and clinical trials through technical innovation and collaboration.\nThis opportunity lies within analytical development for synthetic molecules, where cutting-edge techniques like high-performance liquid chromatography, gas\u002Fion chromatography, and mass spectrometry are employed to develop efficient and robust analytical methods. The goal is to ensure the release of clinical trial products and their eventual commercial supply through a strong control strategy.\nTake the lead in pioneering innovative analytical techniques while contributing to the successful delivery of clinical and commercial therapies-apply now and help shape the future of healthcare!\nThe Perfect Candidate:\nThe perfect candidate holds an advanced degree in chemistry or pharmacy and brings a minimum of five years of professional experience in the analytical development of synthetic drug substances. They are a technical expert in liquid chromatography (including HPLC, UHPLC, and advanced detection methods like MS) who can independently drive the development of analytical control packages for intermediates and APIs. As a natural leader and communicator with an excellent command of English, they excel at coaching junior staff, managing external CDMO\u002FCLO activities, and collaborating cross-functionally to deliver seamless project execution. Finally, they possess strong digital acumen, a rigorous approach to statistical data, and proven experience authoring critical regulatory dossiers (such as NDAs) to ensure total data integrity.\nTasks & Responsibilities:\n* Serve as the Analytical SME\u002Fanalytical project lead (APL), driving the development of state-of-the-art analytical control packages for synthetic molecules, including direct materials, IPCs, intermediates, and crude APIs.\n* Actively contribute to portfolio delivery by ensuring efficient and effective process development analytics, including the adoption of modern techniques like modeling and simulation.\n* Coaching technicians and junior scientists on project work and serving as a central point of contact for project-related information\n* Supervise internal laboratory activities and \u002F or testing activities at CLOs\u002FCDMOs\n* Collaborate cross-functionally with key partners in research and early development, Regulatory, and Quality to ensure seamless project execution and alignment.\n* Author, review, and approve critical documents and regulatory dossiers (e.g., QIMPD, NDA) while ensuring compliance with quality standards and data integrity.\n* Act as a Chemistry Project Lead (CPL), leading external testing activities at CDMOs or CLOs, and contributing to the hiring and coaching of new colleagues.\nMust Haves:\n* A Master’s or Ph.D. in chemistry, pharmacy, or a related field\n* Min. 5 years of professional experience within the analytical development of synthetic molecules drug substances\n* A robust foundation in liquid chromatography (HPLC and UHPLC) with proficiency in various detection methods, including UV, Mass Spectrometry (MS), fluorescence, and charged aerosol detection\n* You possess a solid understanding of analytical chemistry, particularly chromatographic techniques (HPLC, GC), titrations, and various physicochemical methods.\n* You demonstrate excellent collaboration, technical supervision, and project management skills, with a structured and rigorous approach\n* Digital acumen to support digital transformation initiatives; familiarity with statistical analysis of analytical data is also advantageous\n* Excellent command of the English language.\nNice to Haves:\n* Proficiency in German is considered a plus\nReference Nr.: 924992\nRolle: Technical R&D – Analytical Project Lead\nIndustrie: Pharma\nLocation: Basel\nPensum: 100%\nStart: ASAP (01.08.2026)\nDuration: 12+ months\nDeadline: 08\u002F06\u002F2026\nIf this position has piqued your interest, please send us your complete resume. If this position does not quite match your profile and you would like to receive other positions directly, you can also send us your resume via this ad or to jobs[at]itcag[dot]com.\nContact us for more information about our company, our positions, or our attractive payroll-only program: +41 41 760 77 01.\nAbout us:\nITech Consult is an ISO 9001:2015-certified Swiss company with offices in Germany and Ireland. ITech Consult specializes in placing highly qualified candidates for temporary staffing in the fields of IT, life sciences, and engineering. We offer temporary staffing and payroll services. This is free of charge for our candidates, and we do not charge any additional fees for payroll services.\nApply Now\n\nIndustry\nPharmaceuticals\nLocation\nBasel\nType\ntemporary\n\nE-Mail: service@itcag.com","Wir suchen einen erfahrenen Analytical Project Lead für unser Technical R&D Team im Bereich synthetischer Moleküle. In dieser Position übernehmen Sie die fachliche Führung bei der Entwicklung innovativer analytischer Methoden für Arzneimittelwirkstoffe und tragen maßgeblich zur Bereitstellung klinischer und kommerzieller Therapien bei.\n\nIhre Hauptaufgaben umfassen die Entwicklung modernster analytischer Kontrollpakete für synthetische Moleküle, einschließlich Ausgangsmaterialien, Zwischenprodukten und APIs. Sie fungieren als Subject Matter Expert und treiben die Implementierung fortschrittlicher Techniken wie HPLC, UHPLC, Massenspektrometrie und UV-Detektion voran. Dabei arbeiten Sie eng mit internen Teams sowie externen Partnern zusammen und stellen sicher, dass alle analytischen Entwicklungen den höchsten Qualitätsstandards entsprechen.\n\nZu Ihren Verantwortlichkeiten gehört auch die fachliche Betreuung von Technikern und Nachwuchswissenschaftlern sowie die Überwachung von Laboraktivitäten. Sie erstellen und prüfen regulatorische Dokumentationen und arbeiten abteilungsübergreifend mit Forschung, Entwicklung, Regulatory Affairs und Quality zusammen.\n\nWir erwarten einen Hochschulabschluss in Chemie oder Pharmazie sowie mindestens fünf Jahre Berufserfahrung in der analytischen Entwicklung synthetischer Arzneimittelwirkstoffe. Sie verfügen über fundierte Expertise in der Flüssigchromatographie und modernen Detektionsmethoden. Ausgezeichnete Englischkenntnisse, Führungsqualitäten und Erfahrung in der Erstellung regulatorischer Dossiers runden Ihr Profil ab. Diese Position bietet die Möglichkeit, an der Spitze analytischer Innovation zu stehen und die Zukunft der Gesundheitsversorgung mitzugestalten.","en","924992","https:\u002F\u002Fwww.itcag.com\u002Fjobs\u002Ftechnical-rd-analytical-project-lead-8114\u002F",{"items":34},[35,57,74,90,106,124,136,148,165,180,196,216,227,245,266],{"id":36,"slug":37,"title":38,"skills":39,"budget":18,"duration":51,"location":52,"onsitePercent":53,"contractType":54,"foundAt":55,"category":56},7364,"stellv-leitung-der-herstellung","Stellv. Leitung der Herstellung",[40,41,42,43,44,45,46,47,48,49,50],"Pharmatechnik","Biotechnologie","GMP","Aseptische Abfüllung","Batch Record Review","Change Controls","CAPA","OEE-Systeme","Shopfloor-Management","Lean","OPEX","24 Monate (01.07.2026 - 30.06.2028)","Sachsen",100,"contracting","2026-06-01T20:11:17+00:00",{"id":24,"slug":25,"label":26},{"id":58,"slug":59,"title":60,"skills":61,"budget":18,"duration":71,"location":20,"onsitePercent":18,"contractType":21,"foundAt":72,"category":73},7349,"rezept-und-methoden-spezialist","Rezept- und Methoden-Spezialist",[62,63,64,65,42,66,67,68,41,69,70],"Chemie- und Pharmatechnologie","PLS\u002FMES","PCS7","Unicorn Methodenrezeptierung","SOP","Qualitätssicherung","MSAT","Siemens","SAP","01.09.2026 bis 30.08.2027","2026-06-01T16:12:07+00:00",{"id":24,"slug":25,"label":26},{"id":75,"slug":76,"title":77,"skills":78,"budget":18,"duration":51,"location":86,"onsitePercent":87,"contractType":54,"foundAt":88,"category":89},7348,"stellvertretung-leitung-der-herstellung-amwhv","Stellvertretung Leitung der Herstellung (AMWHV)",[40,41,42,79,80,81,82,47,48,83,84,85,49,50,44,45,46],"Sterilabfüllung","aseptischer Bereich","Zytostatika","Drug Substance","AMWHV","AMG","US-FDA","Dessau-Roßlau",80,"2026-06-01T16:10:58+00:00",{"id":24,"slug":25,"label":26},{"id":91,"slug":92,"title":93,"skills":94,"budget":18,"duration":18,"location":103,"onsitePercent":53,"contractType":54,"foundAt":104,"category":105},7333,"packaging-labeling-spezialist-pharma-mwd","Packaging & Labeling Spezialist Pharma (m\u002Fw\u002Fd)",[95,96,42,97,98,99,100,101,102],"Biologie","Chemie","GDP","Pharmazie","Risikomanagement","MS Office","LIMS","Projektmanagement","Biberach","2026-06-01T15:26:29+00:00",{"id":24,"slug":25,"label":26},{"id":107,"slug":108,"title":109,"skills":110,"budget":18,"duration":18,"location":121,"onsitePercent":53,"contractType":54,"foundAt":122,"category":123},6439,"clinical-compliance-specialist-mwd-medical-devices","Clinical Compliance Specialist (m\u002Fw\u002Fd) Medical Devices",[111,112,113,114,115,116,117,118,119,120],"Clinical Evaluation","Medical Writing","MDR","ISO 14155","Post-Market Clinical Follow-up","Systematische Literaturrecherche","Medizinprodukte","Statistik","Zahnmedizin","Regulatorische Anforderungen","Bensheim","2026-05-28T07:25:35+00:00",{"id":24,"slug":25,"label":26},{"id":125,"slug":126,"title":127,"skills":128,"budget":18,"duration":18,"location":132,"onsitePercent":133,"contractType":54,"foundAt":134,"category":135},6425,"quality-specialist-pharma-mwd","Quality Specialist Pharma (m\u002Fw\u002Fd)",[42,129,98,41,96,99,130,131],"Qualitätsmanagement","Audits","Teamfähigkeit","Biberach an der Riß",50,"2026-05-28T06:25:31+00:00",{"id":24,"slug":25,"label":26},{"id":137,"slug":138,"title":139,"skills":140,"budget":18,"duration":18,"location":145,"onsitePercent":133,"contractType":54,"foundAt":146,"category":147},6392,"qualitaetsmanager-mwd-medizintechnik","Qualitätsmanager (m\u002Fw\u002Fd) Medizintechnik",[129,26,141,130,100,142,143,144],"DIN 13485","Reklamationsmanagement","Validierung","Qualifizierung","Schwerin","2026-05-28T02:26:01+00:00",{"id":24,"slug":25,"label":26},{"id":149,"slug":150,"title":151,"skills":152,"budget":18,"duration":18,"location":162,"onsitePercent":133,"contractType":54,"foundAt":163,"category":164},6391,"experte-bildverarbeitung-medizintechnik-mwd","Experte Bildverarbeitung Medizintechnik (m\u002Fw\u002Fd)",[153,154,155,26,156,157,158,159,160,161],"Bildverarbeitung","C++","Python","Algorithmusentwicklung","Physik","Informatik","Sensoren","Bildfilterung","Rekonstruktion","Mannheim","2026-05-28T02:25:47+00:00",{"id":24,"slug":25,"label":26},{"id":166,"slug":167,"title":168,"skills":169,"budget":18,"duration":18,"location":132,"onsitePercent":53,"contractType":54,"foundAt":178,"category":179},6390,"technischer-assistent-mwd-wasseranalytik","Technischer Assistent (m\u002Fw\u002Fd) Wasseranalytik",[170,171,172,173,174,42,175,176,177,144,143],"Biologielaborant","BTA","MTA","mikrobiologische Testmethoden","Environmental Monitoring","Dateneingabe","Dokumentation","Monitoring","2026-05-28T02:25:33+00:00",{"id":24,"slug":25,"label":26},{"id":181,"slug":182,"title":183,"skills":184,"budget":18,"duration":18,"location":193,"onsitePercent":133,"contractType":54,"foundAt":194,"category":195},6262,"softwareentwickler-c-medizintechnik-mwd","Softwareentwickler C++ Medizintechnik (m\u002Fw\u002Fd)",[154,185,186,187,188,189,190,26,191,192],"C#","C","CAN-Bus","Softwarearchitektur","Softwareentwicklung","Unit-Tests","Elektrotechnik","SCRUM","Jena","2026-05-27T11:28:50+00:00",{"id":24,"slug":25,"label":26},{"id":197,"slug":198,"title":199,"skills":200,"budget":18,"duration":19,"location":213,"onsitePercent":18,"contractType":21,"foundAt":214,"category":215},6245,"requirement-engineer","Requirement engineer",[201,202,203,204,205,206,207,208,209,210,211,212,17],"Requirements Engineering","ALM","CPRE\u002FIREB","CCBA\u002FIIBA","INCOSE","System Engineering","Software Engineering","Medical Engineering","IVD","V-model","EARS","German","Rotkreuz","2026-05-27T10:36:37+00:00",{"id":24,"slug":25,"label":26},{"id":217,"slug":218,"title":219,"skills":220,"budget":18,"duration":18,"location":224,"onsitePercent":18,"contractType":54,"foundAt":225,"category":226},6225,"requirement-engineer-hardwaresoftware-mfd","Requirement engineer Hardware\u002FSoftware (m\u002Ff\u002Fd)",[201,211,210,221,222,223,209,212,17],"System Development","ALM tools","Medical Devices","Zug","2026-05-27T10:06:13+00:00",{"id":24,"slug":25,"label":26},{"id":228,"slug":229,"title":230,"skills":231,"budget":18,"duration":240,"location":241,"onsitePercent":242,"contractType":54,"foundAt":243,"category":244},6186,"senior-qa-compliance-expert-2","Senior QA Compliance Expert",[42,232,233,234,46,235,236,237,238,70,239,98,96,95],"Quality Assurance","Compliance","Deviation Management","Change Control","EU-GMP-Leitfaden","ICH-Richtlinien","TrackWise Digital","S4 HANA","11. Mai 2026 bis 31. März 2027","München",20,"2026-05-27T08:11:21+00:00",{"id":24,"slug":25,"label":26},{"id":246,"slug":247,"title":248,"skills":249,"budget":18,"duration":19,"location":213,"onsitePercent":18,"contractType":21,"foundAt":264,"category":265},6181,"msat-engineer-process-management-2","MSAT Engineer Process Management",[250,251,252,233,253,254,70,234,255,256,257,258,259,260,261,262,263],"Process Management","Product Development","GxP","Quality Management","Root Cause Analysis","Process Optimization","Regulatory Compliance","Audit Readiness","Biotechnology","Biology","Chemistry","Material Science","Mechanical Engineering","Electrical Engineering","2026-05-27T07:36:42+00:00",{"id":24,"slug":25,"label":26},{"id":267,"slug":268,"title":248,"skills":269,"budget":18,"duration":19,"location":213,"onsitePercent":53,"contractType":271,"foundAt":272,"category":273},6167,"msat-engineer-process-management",[270,251,252,233,253,254,70,234,255,212,17],"Process Development","permanent","2026-05-27T07:21:17+00:00",{"id":24,"slug":25,"label":26}]