Ich Q10 Jobs in Lagos
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Job Description: Preparation of protocol for CT. ICF CRF authoring & quality review. Preparing & writing CSR as per ICH guidelines. Literature survey feasibility check. Prepare & submit documents related to IEC/DCGI for approval. Knowledge of ICH guidelines GCP & applicable regulatio More...
Principal Duties Responsibilities Perform and implement under supervision the following for clinical studies: (i) the SAS programming testing and documentation of statistical programs for use in creating statistical tables figures listings and graphs and (ii) the progra More...
Jako firma specjalizujca si w doradztwie i produkcji oprogramowania Visiativ opiera si na usugach i rozwizaniach z zakresu cyfryzacji aby wspiera naszych klientw we Francji i na arenie midzynarodowej w ich transformacji cyfrowej. Nasze zespoy w Visiativ pracuj nad: Rozwojem przyszych More...
Die Firma: Das Unternehmen ist ein globales Finanzunternehmen im Investmentbereich.TasksDeine Aufgaben sind unter anderem: Reiseplanung und OrganisationOrganisation von Meetings Organisation von Events fr das Team und KundenTelefonkorrespondenzEMailKorrespondenzenUntersttzung des Team More...
QUALIFICATIONS NEEDED: Degree or diploma in Chemistry / Analytical Chemistry / Biochemistry /Biotechnology or equivalent. NECESSARY EXPERIENCE AND INDUSTRY KNOWLEDGE: At least 8 years of experience in the vaccine/pharmaceutical/biotech manufacturing industry. At least 5 years o More...
Quality Control Lead Chemistry Material Handling Pharma
Abc Worldwide -
Cape Town
-
South Africa
QUALIFICATIONS NEEDED: Degree or diploma in Chemistry / Analytical Chemistry / Biochemistry /Biotechnology or equivalent. NECESSARY EXPERIENCE AND INDUSTRY KNOWLEDGE: At least 8 years of experience in the vaccine/pharmaceutical/biotech manufacturing industry. At least 5 years More...
Regulatory Affairs OfficerLocation: Delhi (Office Only)Experience: 25 YearsMustHave: USFDA Regulation 510(K) Compliance as per 21CFR 821. Coordinate with QC QA R&D MSAT Regulatory affairs teams on daytoday activities.Job Responsibility Responsible for product submis More...
Fr unseren Mandanten einen beraus erfolgreichen Projektentwickler im Bereich der Erneuerbaren Energien suchen wir aktuell einem Netzanschlussmanager (m/w/d) an den Standorten Rostock Bielefeld Dresden und Cottbus.TasksBeratung bei der Konzeptionierung von Umspannwerksanschlssenberwach More...
Miejsce pracy: WarszawaHybrydowy model pracy: min. 3 dni pracy z biura w tygodniuPENY ETATTWJ ZAKRES ZADA:Opracowywanie i przygotowywanie instrukcji obsugi do urzdze z danego asortymentu zajmujemy si sprzeda m.in. urzdze do gastronomii elektronarzdzi jeeli wiesz jak obsuy tego typu More...
Full Knowledge of cGMP/GSDP guidelines Knowledge of national/international guidelines and references (FDA, EU, PICs, ICH, etc) Experience in writing and reviewing SOP's, systems, protocols , reports , etc. Experience in the quality management system (QMS) Experience in condu More...
Noema Pharma is a clinicalstage biotech company targeting debilitating central nervous system (CNS) disorders characterized by imbalanced neuronal networks.At Noema Pharma every patient matters.Our pipeline contains novel therapies designed to address debilitating CNS disorders in ord More...
Field Service Engineer EMEA (m/w/d)Standort: Kirchheim bei MnchenVollzeit (40 Stunden)Unbefristete DirekteinstellungDie Firma: Das Unternehmen ist einer der fhrenden internationalen Hersteller von Fertigungsanlagen Komponenten und Systemen in der Vakuumtechnologie. Garant ihres Erfolg More...
Twoje obowizki:Odbir kontenerw od firmy logistycznej i przewiezienie ich do pociguOferujemy:stawkaNOK za godzin od projektu bruttozakwaterowanie w pokoju jednoosobowym w cenie 2600 NOK/miesic lub bezpatne zakwaterowanie w chatce robotniczej (wsplna kuchnia i azienka)praca pon. wt. r. More...
Miejsce pracy: Zielona GraHybrydowy model pracy: min. 3 dni pracy z biura w tygodniuPENY ETATTWJ ZAKRES ZADA:Przygotowywanie projektw graficznych instrukcji obsugi naszych produktwTumaczenia maszynowe instrukcji obsugi (z jzyka angielskiego na 14 jzykw) przy uyciu SMARTCATAktualizacja More...
Website : Position: Documentation Executive Number of Positions: 01 Minimum Experience: 8 years Responsibilities: Expert in preparing validation and transfer protocols/reports as per Anvisa and ICH within proposed timelines. Preparation of SOP Specification STP AMC schedule. More...
Responsibilities: Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring the recording of trial in compliance with project goals. Creating and implementing study-specific clinical monitoring tools and documents. Creating and overseeing the t More...
Jako firma specjalizujca si w doradztwie i produkcji oprogramowania Visiativ opiera si na usugach i rozwizaniach z zakresu cyfryzacji aby wspiera naszych klientw we Francji i na arenie midzynarodowej w ich transformacji cyfrowej. Nasze zespoy w Visiativ pracuj nad: Rozwojem przyszych More...
Fremont CA Contract Duration: 3036 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a QC Associate III in the Fremont CA area. Performs tasks and activities related to supplier/material qualifications and supplier change notifications (e.g. review of v More...
Manage and coordinate the Validation and Calibration activities and follow-up on the related activities to ensure that all activates are compliant to industry standards and GMP requirements. Manage the process validation activities to ensure product / process validation is complian More...
Na czym bdzie polega Twoja praca Wsppracy z dziaem Produkcji Logistyki Laboratorium oraz Prototypw Wspomaganiu i monitorowaniu procesu przygotowywania prototypw Organizowaniu terminowej budowy moduw oraz ich wysyek do klienta Zlecaniu wykonania testw moduw oraz analizie wynik More...
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