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D%EF%BF%BD%EF%BF%BDveloppement%20du%20m%EF%BF%BD%EF%BF%BDdicament [3 offres]
167413 | Étudiant·e - Affaire règlementaire et pharmacovigilance |
Date limite 18 mai 2024 Description du poste
Description des tâches: Conditions Lieu de travail : Canada , Laval Statut d'emploi: Stage Type d'emploi: Temps plein (40 heures) Date d'entrée en fonction: Immédiatement Salaire : NC Autre(s) avantage(s): n/d Exigences Être diplomé Discipline(s) d'études : Développement du médicament Pharmacie/Pratique pharmaceutique / Sciences pharmaceutiques Pharmacologie Cycle(s) d'études : Baccalauréat Exigence(s) linguistique(s) : Français parlé. Anglais parlé. Français écrit. Anglais écrit. Autre(s) exigence(s) : n/d |
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165647 | QC Scientist, Pharmaron Biologics (offre rédigée en anglais seulement) |
Date limite 2 mai 2024 Description du poste
Responsible for QC sample testing and release as well as problem solving, as an expert in QC analysis methods, lead the transfer, validation and optimization of analysis methods. Responsibilities As an expert in QC methods, you are responsible for researching and understanding the principles of basic QC testing methods, instrument principles and being able to promptly identify and solve QC method problems. Implement and follow QC laboratory GMP standard operating procedures to complete the testing tasks of raw materials and products, write and upgrade QC testing methods, record testing data on time, complete corresponding reports, and ensure the truth and integrity of data. To participate in the establishment of quality specifications for raw materials and products, and provide scientific justification for the establishment of quality specifications. Participate in OOS/OOT and deviation investigation in the laboratory Support internal/external and regulatory agency audits. Lead method transfer and validation activities. Support QC project management. Interaction and collaboration with analytical development department or third party services. Conditions Lieu de travail : International , Ningbo Statut d'emploi: Permanent Type d'emploi: Temps plein (8 heures) Date d'entrée en fonction: Immédiatement Salaire : Minimum is 300k RMB/Year Autre(s) avantage(s): We have free hair salon,free on site Gym-free fitness class, free parking, meal subsidy.... different work site have different benefit, for more information, please talk with HR Exigences Être étudiant ou diplômé Catégorie(s) : Recherche Génie Offres générales exigeants des études universitaires Discipline(s) d'études : Biochimie Biologie moléculaire Développement du médicament Pharmacologie Sciences biologiques Sciences biomédicales / Génie biomédical Cycle(s) d'études : Doctorat Exigence(s) linguistique(s) : Anglais écrit. Autre(s) exigence(s) : PhD in basic science or engineering, with a certain level of knowledge in the field of biopharmaceuticals is preferred Have a certain depth of hands-on ability and problem solving experience in physicochemical or biochemical analysis methods and in vitro cell detection. Proficient in common protein analysis methods, biological activity detection methods, as well as their methodology and applications. Having experience in various (or partial) analytical techniques such as HPLC, CE, cIEF, ELISA, LC-MS, ELISA, biossay, osmolarity, endotoxin, moisture content (Karl Fischer), TOC, particle analysis of injected drugs, and process impurity analysis (rDNA, rHCP, rProA). Understand the production process of biopharmaceuticals, especially monoclonal antibodies. Having good teamwork, communication, and organizational skills. Proficient in both Chinese and English. |
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165653 | Pharmacokinetics Researcher (Pharmaceutical Analysis) (Offre rédigée en anglais seulement) |
Date limite 2 mai 2024 Description du poste
You will have the opportunity to participate domestic and international pharmaceutical conferences and communicate with experts in the industry. Job responsibility In vitro pharmacokinetics direction: 1. Use in vitro models or related biological substrates (plasma, cells, microsomes, buffer, etc.) to conduct in vitro screening tests of drug candidates, including physical and chemical properties, drug distribution, drug metabolism and drug-drug interaction; 2, Perform sample analysis using high performance liquid phase and triple quadrupole mass spectrometry tandem technology and high-resolution mass spectrometer; 3. Design and carry out in vitro drug metabolism experiments, collect and sort out experimental data, and prepare experimental protocols and reports. in vivo Pharmacokinetic: 1. Using LC-MS to analyze drugs and metabolites in biological samples (animal blood, tissues, etc.) and conduct PK/PD correlation research; 2, the use of analytical instruments (HPLC, LC/MS/MS) to examine the reaction of the efficacy in the body, the detection of the drug concentration; 3. Design and carry out in vivo drug metabolism experiments, collect and sort out experimental data, and prepare experimental protocols and reports. Job requirements 1, Pharmacy, pharmacology, pharmaceutical analysis, drug metabolism, pharmaceutical chemistry, natural pharmaceutical chemistry, biology or other related major or research direction, doctoral degree; 2. Familiar with the process of new drug research and development, solid professional knowledge and theoretical foundation, proficient in liquid chromatography-mass spectrometry and other related technologies, familiar with the design and operation of preclinical pharmacokinetic experimental schemes, pharmacokinetic software and calculation methods; 3, love the pharmaceutical research and development industry, with fast learning ability and adaptability, good analytical skills, communication and coordination skills and team spirit, leadership, a strong sense of responsibility. 4, with good scientific research ability, able to independently undertake projects, develop project plans, and lead the team to solve problems in the project; 5, English and Chinese proficiency, good English communication, reading English literature and writing English experimental plan ability. Conditions Lieu de travail : Région de Montréal , Beijing, Ningbo Statut d'emploi: Permanent Type d'emploi: Temps plein (8 heures) Date d'entrée en fonction: Immédiatement Salaire : Minimum is 300k RMB/Year Autre(s) avantage(s): n/d Exigences Être diplomé Catégorie(s) : Recherche Discipline(s) d'études : Biochimie Biologie moléculaire Chimie Développement du médicament Microbiologie et immunologie Pathologie et biologie cellulaire Pharmacologie Sciences biomédicales / Génie biomédical Cycle(s) d'études : Doctorat Exigence(s) linguistique(s) : Chinese Autre(s) exigence(s) : n/d |