AddressPresent in more than 100 countries, Virbac is a specialist animal health company with our core business in sheep and cattle products, veterinary pharmaceuticals, as well as a wide range of products for dogs, cats, and horses. Our focus is to shape the future of animal health.
Although we have the support of a global network, we are a company that feels like family. Our people are our strength; thanks to them and a manufacturing base that meets the highest international quality standards, Virbac has been able to forge solid relationships with veterinarians, farmers, and pet owners in each country for more than 50 years.
We're seeking a dynamic individual to join our team of Validation Engineers on a 12 month fixed-term contract.
The Validation department has a position available for a bright enthusiastic person interested in joining the Validation team based at our Penrith manufacturing facility.
This is an ideal opportunity for you to demonstrate your knowledge in validation of sterile, endoparasiticide, ectoparasiticide, paste, powder, solid dose manufacture/testing and distribution activities.
The primary purpose of this position is the management of the day to day running of assigned validation activities as per Validation Master Plan. The role encompasses:
- Validation studies
- Complete assigned activities in the Validation Master Plan
- Conduct risk assessments
- Prepare protocols and reports for validation activities
- Support introduction of new equipment, processes and products
- Support of deviation investigations.
The successful candidate will possess the following qualities:
Behavioural Attributes
- The ability to communicate effectively, with focus on written reports
- Able to analyse problems and situations
- A growth mindset, drive and results orientation
- Demonstrate teamwork and cross functional collaboration
- Ability to work autonomously with high level guidance.
Core Competencies
- Understanding of the APVMA GMP code and related guidelines.
- Knowledge of fundamentals of validation, microbiology, process control, calibration and statistics
- Basic project management skills and tools
- Experience in validation of aseptic manufacturing process line, sterilisation- steam-in place and steam sterilisers (autoclaves) is highly desirable.
- Experience in facility and equipment qualificationis highly desirable
- Experience in-cleaning validation, process validation, computerised system validation and analytical validations is preferred.
A current driver’s license is essential as travel between the Virbac Australia sites and contractor visits is required to complete validation activities.
A tertiary qualification in science and/or engineering complemented with similar experience in pharmaceutical companies is essential.
If you're ready to embark on this exciting journey and have the right attributes and experience, please apply.
Virbac is an equal opportunity employer who believes diversity of thought, background and experience strengthens relationships and benefits our people, clients, and communities.
We are committed to cultivate an inclusive and high-performing culture where our people thrive and are proud to bring their whole selves to work, inspiring a respectful and inclusive environment.
