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Technical Services Supervisor

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Onsite

Technical Services Supervisor

Bora Pharmaceuticals

Technical Services Supervisor

Skills

Process ImprovementCompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Taoyuan, Taoyuan District, Taoyuan City, Taiwan

Work mode:

Onsite

Published on:

2 September 2026

What they need


Job Summary:

Supervisor of Technical Services Department, responsible for supporting new project evaluation, product transfering, production process validation, the operation and maintenance of process and improvement of manufacturing process.

Responsibilities:

  • Coordinate and ensure timely execution of Validation Master Plan activities, including process performance qualification, aseptic process simulation, and related validation tasks, while maintaining compliance with regulatory requirements.
  • Assist in client communication, technology transfer documents preparation, batch execution and project tracking activities to meet project milestones and address real-time changes.
  • Support the development and implementation of effective site procedures for qualification, validation, technology transfer, and process improvements in alignment with industry standards and company policies.
  • Set performance metrics for the technical service team, monitor progress against objectives, and report updates to management.
  • Collaborate with the technical team to identify and implement solutions for technical issues and recommend process improvements based on experimental results, regulatory standards, and business goals.
  • Conduct investigations into deviations or technical issues in commercial production and provide technical guidance to resolve root causes effectively.
  • Organize and deliver formal and informal training sessions for team members to ensure continuous development and compliance with regulatory expectations.
  • Assist in preparing budgets and resource plans for technical service activities and ensure alignment with department goals.

Qualifications:

  • Bachelor's degree in Pharmacy, Chemical Engineering, Biotechnology or related science discipline and over 3 years of related experience.
  • Technical writing skills of GMP documents.
  • Proven track record of process development, process optimization, and technology transfer experience.
  • Ability to work with cross functional teams and meet performance commitments.
  • Speaking and writing skills in both English and Mandarin.

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