水平: Mid-Senior level

工作类型: Full-time

Loading ...

工作内容

  • Competitive salary with a multinational environment with expansion outlook.
  • Work with top manufacturing function with cutting-edge technology.

About Our Client

Our client is a leading pharmaceutical corporation with Taiwan being a regional hub, serving the healthcare demand for different regions. Mainly focusing on business in APAC and best known for its oral cancer medication and generic drugs. With both national and international merits, it is committed to the R&D and manufacturing for highest quality meditations.

Job Description

  • Review GMP manufacturing documents, testing documents and certificates of analysis.
  • Ensure successful operations of QA and good timelines in Operation department.
  • Lead the investigation of non-conformances and follow-up corrective actions in compliance with quality policies and regulations.
  • Provide feedback and manage technical skill development and job performance of employees, encouraging them as well.
  • Qualification documentation review & approval.
  • Meet the annual goal of the company and handle quality management review (quality board and related KPIs).

The Successful Applicant

  • This role is based in Nantou City.
  • 8+ years working experiences in QA with people management experience in Pharmaceutical industry.
  • Fluent in spoken and written English is crucial for communication.
  • Expert in FDA guidelines and cGMP compliance requirements.
  • Strong conflict management ability.
  • Excellent in skills of communication, decision-making, problem-solving, and time management.
  • Able to identify and evaluate risks.
  • Outstanding leadership in multi-functional teams.
  • Able to write documents and lead projects for the site.

What’s On Offer

  • Competitive package and corporate benefits.
  • An important and essential role to maintain the high GMP quality production.

Contact: Ivy Chi

Quote job ref: 4223078
Loading ...
Loading ...

最后期限: 20-12-2024

点击免费申请候选人

申请

Loading ...

相同的工作

Loading ...
Loading ...