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Job Title:  Associate Analyst     
Provided Salary:   Negotiable Work Type:   Full-time
Education:   Bachelor Work Place:   Macao China
Number Of Vacancies:   1 Work Experience:   Not Available
Updated Date:   2024-05-29 Job Type:  
Manufacturing
Certification Requirements:  

Position Requirement:
  • Associate Analyst

    Job Mission:

     

    Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.


    Main Responsibilities:


    • Follow the daily priorities in order to accurately and promptly perform the allocated sample analysis.
    • To adhere to the laboratory testing schedule in order to achieve an efficient Quality Control (QC) system.
    • Take responsibility for all data individually generated and ensure it is in accordance with all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities.
    • To maintain all checklists, laboratory records and notebooks in which he/she is involved to an acceptable GMP standard and in accordance with Hovione internal procedures.
    • To issue events and support the investigation of OOS/OOT/atypical results, deviations and QC incidents generated in the QC Laboratories.
    • Ensure facility activities are carried out in compliance with all GMP, legal and HSE regulations and applicable standards in the country of operation, complying with and enforcing all Hovione processes and good practice.


    Profile:


    • Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (preferable)
    • Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (preferable)
    • Competent (written and verbal) English
    • Technical understanding of GMP practices, analytical theory and techniques


    We offer:


    • Global career development
    • Integration into a dynamic technical team of an International Company
    • Attractive remuneration, fringe benefits include bonus, canteen, transportation and medical scheme.



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