Job Description

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Regulatory Affairs Officer

Advertiser: treidlia biovetMore jobs from this company

Job Information

Job Listing Date
18 Jan 2019
Location
Sydney, Parramatta & Western Suburbs
Work Type
Full Time
Classification
Science & Technology, Biotechnology & Genetics
  • Are you a strategic, critical thinker?
  • Do you want to make a real difference to animal health and wellbeing?
  • Are you excited by innovation?

About us
Tréidlia Biovet is a leading manufacturer of specialty veterinary vaccines based at Seven Hills, Sydney, NSW. The company produces a range of varied and interesting products.

About the role
Due to continued growth, we are seeking a proactive, positive team player to join our company as a Regulatory Affairs Officer.

This position involves the preparation and management of applications as required for the Regulatory Affairs and R&D activities of the Company in Australia, New Zealand and further afield. Previous experience in Regulatory Affairs as it relates to vaccines and the animal health industry would be highly advantageous, however training could be provided.

The position could be steered towards a more senior or more junior applicant. Full time is preferred but there may be some possibility for part-time work.

Key duties

  • Assisting with the compilation, submission and management of applications to Australian Pesticides and Veterinary Medicines Authority, Department of Agriculture and Water Resources and Office of the Gene Technology Regulator.
  • Managing existing permits and licenses i.e. submitting annual reports or applying for extensions or renewals.
  • Ensuring that all starting materials used in manufacture have regulatory approval
  • Liaising with the R&D team throughout the development process to monitor, quality check and streamline submission of new applications.
  • Liaising with external bodies such as universities with which the company is involved in collaborative projects.
  • Liaising with the Quality and Production departments regarding compliance with Permit and/or license conditions.
  • Liaising and meeting with government regulatory agencies.
  • Participating in regular meetings and forums including our Institutional Biosafety Committee.
  • Representing the company at scientific and regulatory seminars and conferences
  • Other duties as may be required from time to time

Skills and experience

  • Tertiary qualification in a Life Science discipline, ideally with a focus on microbiology, molecular biology or Veterinary Science.
  • Demonstrated superior written, verbal & interpersonal communication skills.
  • Demonstrated ability to produce accurate, high quality reports.
  • Demonstrated capacity for critical and strategic thinking.
  • Exceptional attention to detail.
  • Ability to work independently while following directives.
  • Time management and multi-tasking skills.
  • Good computing and data analysis skills.
  • Project management skills.
  • Experience in Regulatory Affairs or Research and Development in the animal health sector, particularly vaccines, is highly desirable.

Benefits and perks

  • Interesting and varied work
  • Innovative new technologies 
  • Fast developing business 
  • Competitive salary package 
  • Attendance at seminars and conferences
  • Free on-site parking
  • Diverse workforce
  • Work/life balance with flexible hours 
  • Family focused

How to apply
Please call Mark White for a confidential discussion on 02 9674 1488 or apply through seek with your cover letter and resume.

The application form will include these questions:
  • Which of the following statements best describes your right to work in Australia?
  • How much notice are you required to give your current employer?
  • What's your expected annual base salary?
  • What's your highest level of education?
  • Have you completed a qualification in biology?

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