IT Data Analytic Supervisor, Export Regulatory Affairs Officer

thumbnail-cadangan PT Industri Jamu dan Farmasi Sido Muncul Tbk
Position: IT Data Analytic Supervisor
Placement: West Jakarta

  • Candidate must possess at least Bachelor's Degree in Engineering (Computer/Telecommunication), Computer Science or Information Technology.
  • Maximum age 35 years old
  • At least 3 years working experience in the related field is required for this position
  • Comfortable working with various operating systems
  • Ability to develop scripting code
  • Excellent in PHP & MySQL
  • Good knowledge in Tableau and Talend
  • Experience in frameworks (Laravel, Code Igniter)
  • Good knowledge in SQL and Query
  • Experience with Third-Party Libraries and APIs (ISON, HTTP etc)
  • Experience with LINUX, Webserver, Iquery, Java Script, HTML, CSS
  • Good analytical and problem solving
  • Proficient in English
  • Design dan develop application with PHP and MySQL
  • Maintain and adjust existing application
  • Maintain and processing data warehouse and ETL
  • Research on latest open source technologies
  • Monitor and analize current systems to identify potential bugs and potential improvement
  • Maintain current system programs and support improvement web apps
  • Fine tuning website (beginner level)
  • Perform system maintenance to ensure system is running smoothly
Apply via Jobstreet:

PT Industri Jamu dan Farmasi Sido Muncul Tbk
Position: Export Regulatory Affairs Officer
Placement: South Jakarta

  • Candidate must possess at least a Bachelor's Degree, Pharmacy/Pharmacology or equivalent from the reputable university with GPA minimum 3,00
  • At least 3 year(s) of working experience Regulatory Affairs (for Export)
  • Maximum 35 years old
  • Excellent communication skills, Fluent in English both oral and written
  • Computer literacy (Microsoft Office)
  • Has good administration skill
  • Applicants must be willing to work in Cipete Raya, Jakarta Selatan.
  • Preferably Supervisor / Coordinators specializing in Healthcare - Pharmacy or equivalent.
  • Available join ASAP
  • Do all administration task related to registration and export
  • Compile dossier according to valid guideline for several country
  • Ensuring that a company's products comply with the regulations of the MHRA
  • Preparing submissions of license variations and renewals to strict deadlines
  • Monitoring the development process related to the product under the exported product pipeline
  • Monitoring and setting timelines for license variations and renewal approvals
  • Liaise the communication between agent/distributor or regulatory authority and the related department
  • Advising scientists and manufacturers on regulatory requirements
  • Act as project management officer to manage the compliance of the existing product with the approval from BPOM
  • Handle trademark
  • Handle quality assurance compliance for overseas such as complaint, recall, return, inspection.
Apply via Jobstreet:


@TG, 27112021
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