Production Technician

OncoRes Medical was founded at the intersection of medicine, science and humanity to improve the accuracy of breast conserving surgery and eliminate the physical, psychological and economic burdens associated with repeat operations. 

Our unique, informal culture champions vision, restlessness and humanity. Knowing we have an open and supportive team means each of us has the freedom to take responsibility and ownership. We have a shared passion to work restlessly, pioneering change to re-imagine the world, while remaining grounded in our commitment to science and quality. 

Our passion for helping patients focusses us on the patient. We believe that all breast cancer patients deserve the opportunity to move beyond their breast cancer surgery knowing that all the cancer has been removed, the first time. In everything we do, we are thinking about how we can inch closer to a world free from re-excisions... We are going BEYOND BREAST CANCER 

Overview: 

The Production Technician at OncoRes Medical is responsible for the completion of low volume production work according to manufacturing instructions and design documentation to support the delivery of products to clinical trials and customers, supporting the realisation of OncoRes Medical’s product development hardware program. The successful candidate will be a key member of OncoRes Medical’s Hardware Program Team and expected to work collaboratively within a multidisciplinary Research and Development group. 

If you want to use your expertise to help build a novel, disruptive medical product that will impact the lives of millions of people around the world, get in touch! This is a unique opportunity to get involved in an early, rapidly growing company with significant growth and development opportunities for the right candidate. 

Role:

• Low volume manufacture and inspection of medical device components in a controlled manufacturing environment. 
• In-process testing of medical device components to ensure quality, performance, and regulatory compliance. 
• Demonstrate commitment to workplace safety by establishing and maintaining safe working practices. 
• Maintenance of inventory, including supporting the receival, inspection and storage of incoming materials, and packaging, despatch, and shipping of outgoing goods. 
• Conduct preventative maintenance and calibration of products and test equipment. 
• Support of additive manufacturing processes used to prototype products and test equipment. 
• Collaboration with the Research and Development group to identify and support the implementation of improvements in manufacturing processes. 

Responsibilities: 

• Manufacture of medical device components with adherence to manufacturing work instructions. 
• Maintain accurate and complete production records. 
• Ensure production areas are clean, orderly, and safe. 
• Comprehensive testing of medical device components with adherence to test protocols. 
• Routine monitoring and maintenance of controlled manufacturing environment. 
• Manage inventory related to production, including purchasing, inspection, and storage of incoming materials, and packaging, despatch, and shipping of outgoing goods. 
• Operate within a Quality Management System (QMS) based on ISO-13485. 
• Manufacture and testing to support development of new designs and processes. 

Qualifications: 

• Minimum 3 years of experience in production of highly regulated products, preferably medical device manufacture. 
• Strong collaborative skills. 
• Strong attention to detail and a personal dedication to the quality of work performed. 
• Ability to remain professional and positive in all personal interactions, and work with honesty and transparency while being committed to doing what’s best for our patients, customers, and company. 
• Qualified candidates must be legally authorized to be employed in Australia. 

Desirable Experience: 

• Medical or Regulated Device manufacturing compliant with a Quality Management System. 
• Experience performing manufacturing processes within a controlled environment. 
• Completion of manufacturing records according to Good Documentation Practices 

Benefits: 

• Comprehensive and competitive remuneration packaging including Employee Assistance Program and mobile phone allowance. 
• A flexible and fun workplace where we understand that your life is more than your job. 
• A rare opportunity to work closely alongside world class colleagues and mentors with many collective years of experience in all aspects of medical device development and commercialisation. All of us are share a passion to work collaboratively where every voice is heard, and your personal professional development is a high priority. 

OncoRes is committed to building and fostering an inclusive, diverse and safe workplace. We believe the differing perspectives and experiences each of us brings inevitably increases innovation and teamwork, flowing into positive tangible outcomes.