Administration / Business Support

Seeking: Regulatory Affairs/Quality Assurance/Administration

Key skills and experience:

  • Over 6 years of New Zealand experience in Pharmaceutical Regulatory Affairs and document change control procedures and 4 years in laboratory analysis
  • Knowledge and understanding of regulatory and QA systems and ability associated with technical standards development and implementation
  • Prior experience in research and strategic projects
  • High standard of GMP and GLP
  • Well organised person with strong time management skills
  • Able to adapt and develop new techniques and multi-task
  • Excellent communication and management skills
  • Client relationship building and problem-solving abilities, work well under pressure
  • Positive and proactive attitude to work and strong ability to learn new things

Computer skills include: MS Office Suite (Word, Excel, Access, Outlook, PowerPoint, Publisher)

Qualifications: Master of Applied Science; Bachelor of Engineering

Value added: Fluent in Chinese

This candidate is also available for up to four weeks work at no cost or obligation, under the terms of the Migrant Employment Programme.

Call Helen on 09 375 3922 or email to find out more.