WHAT DO YOU NEED?

Our ideal candidate will have a passion for medical or life science engineering who can drive development from prototype to production leading to commercialisation of life saving radiopharmaceutical products.
We are seeking someone who has experience applying engineering principles with strong design control and product development life cycle expertise.

Other key requirements of this role include:

• A Masters or PhD in Mechanical Engineering, Electrical Engineering, Mechatronics, Industrial Design or other relevant discipline
• 5 years or more in a design and development role with a strong emphasis on CAD design and development, ideally within the pharmaceutical or medical device industry
• Knowledge or experience in product development under ISO 13485 would be highly regarded
• Strong proficiency in SolidWorks software
• Sound understanding of GMP regulatory requirements
• Proven experience building, testing and troubleshooting electromechanical process control systems
• Eagerness to be an effective team member of a diverse, inclusive, multi-cultural team environment and strong communication skills and analytical problem-solving skills.

If you think this could be the role for you then please apply now! Or, if you have any questions, please contact Leah Creswick on 0478 193 170.

IF YOU KNOW SOMEONE LOOKING FOR A JOB, REFER THEM TO US AND WE’LL GIVE YOU $500* IF WE FIND THEM A NEW ROLE!

SCR-leah-creswick

ChooseFuse

WHAT WILL YOU BE DOING?

The growing Engineering team relies on 3 key sections – Research, Development and Manufacturing. As the Design Engineer - CAD Expert you will formulate the approach to the development of radiopharmaceutical products and processing systems using SolidWorks.

Key tasks of this role include:

• Design and develop radioisotope generators - Bench-top scale product
• Work with Manufacturing Engineers to develop the prototype to a pilot design
• Iterative prototyping of the novel hardware device
• Independently manage own product design activities
• Provide engineering advice and best practice regarding CAD design activities

Other key requirements of this role include:

• A Masters or PhD in Mechanical Engineering, Electrical Engineering, Mechatronics, Industrial Design or other relevant discipline
• 5 years or more in a design and development role with a strong emphasis on CAD design and development, ideally within the pharmaceutical or medical device industry
• Knowledge or experience in product development under ISO 13485 would be highly regarded
• Strong proficiency in SolidWorks software
• Sound understanding of GMP regulatory requirements
• Proven experience building, testing and troubleshooting electromechanical process control systems
• Eagerness to be an effective team member of a diverse, inclusive, multi-cultural team environment and strong communication skills and analytical problem-solving skills