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Technology Transfer Specialist

Synthorx

Synthorx

IT
Ho Chi Minh City, Vietnam
Posted on Nov 29, 2024

R2774689 Technology Transfer Specialist

  • Location: M&S site, district 9, HCMC
  • Job Type: Permanent, full-time

Job Purpose

Responsible for the execution and successful completion of tasks or projects assigned by the Head of Department. This includes ensuring that project progress and quality align with predefined KPIs and timelines.

Key Accountabilities

  • Task Execution and Reporting
    Ensure timely completion of assigned tasks. Report any deviations to the Head of Department periodically or as requested.

  • Planning and Coordination
    Participate in planning processes and coordinate with other departments to ensure effective execution.

  • Data Analysis and Documentation
    Collaborate with departments to collect information, analyze data, compile documentation, and contribute to production and validation processes.

  • Process Transfer and Trials
    Support and coordinate with the Development Center for trial batches on industrial equipment. Act as the key contact for process and analytical method transfer for products developed by the R&D Center for industrial-scale production.

  • Team Training
    Provide training to new team members on required skills for process validation.

  • Material Management
    Manage tasks related to the preparation of materials and packaging for project implementation.

Qualifications

Education

  • Bachelor’s degree in pharmacy or related fields

Related Experience

  • Minimum 2-3 years of experience in R&D, production, or quality assurance in a pharmaceutical company.
  • Experience in project management and stakeholder management is preferred.
  • Knowledge/experience in pharmaceutical regulations, drug registration, packaging development, or planning is an advantage.

Core Competencies

  • Proficiency in English for communication, documentation, and technical writing (protocols, processes).
  • Effective and professional communication skills.
  • Adaptability and the ability to work in a fast-paced environment.
  • Solid understanding of GMP, pharmaceutical manufacturing, galenic research, validations, and regulations.

Pursue progress, discover extraordinary

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