Quality Pharmacist at Icon Group
Greater Adelaide, South Australia, Australia -
Full Time


Start Date

Immediate

Expiry Date

08 Dec, 25

Salary

0.0

Posted On

09 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

THE OPPORTUNITY

We’re currently seeking a permanent full-time Quality Pharmacist to work in our newly opened state-of-the-art compounding facility in Woodville Adelaide. The work involves preparation and compounding of oncology treatments. Reporting to the Quality Pharmacist Supervisor, you will work closely with the Operations department, providing quality control support to the compounding centre, with a strong continuous improvement focus.
This is a permanent full-time position working a minimum of 76 hours a fortnight, Monday to Friday plus overtime and weekend work on occasion. Shift hours fall between 6:00am and 10:00pm.

ABOUT US

Underpinned by 60 years’ experience, Slade Health is Australia’s leading chemotherapy compounding provider with a commitment to patient care, quality, innovation and integrity.
Slade delivers approximately 1.2 million infusions each year to over 200 hospitals across the public and private healthcare sector, including long-term state-wide government contracts. Slade operates five licensed manufacturing facilities - four in Australia and one in New Zealand, and under Icon Group has recently acquired BathASU (part of Pharmaxo Group) in the United Kingdom. [AM1] Slade Health is a full-service compounder providing antibiotics, chemotherapy, analgesics and theatre lines, and the exclusive compounder in Australia of Fresenius Kabi Total Parenteral Nutrition.
For more information visit https://sladehealth.com.au/

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Responsibilities
  • Releasing all finished products (including oncology, antibiotics, TPN & LAF)
  • Ensure all products are compounded appropriately according to product specifications and documentation to obtain the required quality.
  • Ensure all quality management systems and procedures are adhered to
  • Participate in preparation of new Quality Documents and revision/update of existing documents.
  • Ensure all product non-conformances are evaluated and rejected and/or escalated to quality management in a timely manner
  • Ensure all incidents, deviations and complaints are reported appropriately and document in the QMS in a timely manner
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