About the Company & Role:
Join a TGA‐licensed, Leading Radiopharmaceutical Manufacturer at the forefront of producing innovative diagnostic and therapeutic products. This company is committed to excellence, innovation, and advancing healthcare through cutting‐edge technology.
Role Overview:
As a QC Chemist, you'll work within a small, collaborative team to ensure GMP compliance across the manufacture and release of radiopharmaceutical products. The role involves routine QC testing, data analysis, documentation, and support of deviation investigations to ensure product quality and regulatory compliance.
Duties:
* Perform quality control testing of raw materials and finished products
* Conduct routine equipment troubleshooting, calibration, and general maintenance (HPLC, GC etc.)
* Prepare, manage, and maintain reference standards and reagents
* Analyse data and report results against product specifications
* Maintain accurate and compliant GMP documentation
* Identify, document, and elevate deviations, OOT, and OOS results, and support associated investigations
* Perform validation activities for new and existing equipment, products, and processes
Skills & Experience:
* Tertiary qualifications in Chemistry, Pharmaceutical science, Radiochemistry or a related discipline
* Practical knowledge of analytical instrumentation and analytical techniques
* Excellent documentation and report‐writing skills
* High attention to detail with a strong focus on accuracy and compliance
* Ability to work independently and take initiative
* Comfortable in a fast‐paced, regulated environment
Culture & Benefits:
* Ongoing training and development opportunities
* Free on‐site parking
* Work in a specialised radiopharmaceutical setting making a real impact
* Supportive, collaborative team environment
Apply!
Ready to take the next step in your career? Submit your application today! Please include a detailed resume in Word format. For any questions about the role, contact Mairead on 61 ***********.
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