QUALITY CONTROL TECHNICIAN – GEEBUNG, QLD 

• Dynamic and Supportive Work Environment
• 12 Month Part-Time Contract Position 08:30 – 16:36 Geebung, QLD Location

Slade Health provides a complete range of sterile compounding services, including Chemotherapy, Analgesics, Antibiotics and TPN compounding. With facilities based in Queensland, Victoria, New South Wales and New Zealand, quality is embedded into every stage of the compounding process.

Part of something bigger
Being part of Icon Group, Australia’s largest dedicated cancer care provider, with a global presence in Singapore, Mainland China, Hong Kong and New Zealand. The Group is built on a strong but simple vision – to deliver the best care possible, to as many people as possible, as close to home as possible.

Here’s why our people choose us

Purpose, at Pace: We remain focused on continually expanding our services and making them accessible to more people across Australia and internationally.

Impact, at Scale: We have a global reach and are growing every day. Here you’ll know your work is making a difference.

Connection, at Heart: Our work isn’t easy but it’s extremely important. Our secret ingredient is our incredible, connected, and talented people. And their secret ingredient is each other.

Opportunity, at Hand: We’re continually innovating. Every week brings changes, growth and new opportunities.

The Opportunity
Reporting to the Site Quality Manager, you will work closely with the Operations department, providing quality control support to the compounding centre, with a strong continuous improvement focus. The role is offered on a 12-month part-time contract basis working Monday to Friday between the hours of 08:30 – 16:36 at our Geebung site. Some weekend work and overtime may be required

Key Responsibilities

• Maintain the microbiological, non-viable and chemical monitoring of the compounding centre
• Liaison with external service providers
• Assist in calibration, certification activities and validation of processes and staff
• Coordinate media fills
• Maintain and organise the site micro laboratory
• Coordinate cytotoxic and antibiotic residue monitoring of cleanrooms
• Prepare new Quality Documents and revision/update of existing documents
• Participate in risk assessment activities

About You

• Strong attention to detail, excellent verbal and written communication skills and the ability to comply with PIC/S and documented quality system procedures.
• Tertiary qualifications in a Science discipline (Microbiology/Bio Science).
• Experience in microbiology is desirable.
• Previous experience in a laboratory environment is desirable..
• Previous experience in a cleanroom or GMP-compliant pharmaceutical manufacturing environment would be an advantage.
• Knowledge of TGA PIC/s requirements (preferable)
• Training in GMP and Quality Systems (preferable)
• Working knowledge of continuous improvement philosophy is desirable.

  
Excited to join us?
Our team makes us who we are, they shape our impact and drive our success. So Apply Now and make it happen with Icon.
  
Visit https://icongroup.global/en/careers/our-people/stories/ to read the stories of our incredible people.
  
Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees. We encourage applications from all diverse backgrounds.
  
  
  
Icon is committed to managing the risk of transmission of specified vaccine preventable diseases (VPDs) including COVID-19. Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs.