Analytical / Stability Scientist

• Fantastic Opportunity for a Pharmaceutical professional
• Permanent Rolelocated close to the CBD
• Innovative team culture

Our client is a dynamic and successful Australian pharmaceutical company developing and commercialising a range of specialised pharmaceutical products for the global market. They are currently seeking an experienced Analytical / Stability Scientist to support their analytical team in stability, analytical development / validation, and R&D activities.

Key duties and responsibilities will include:

• Perform QC testing of raw materials, intermediates, components, and finished products.
• Conduct stability studies of various dosage forms utilising a broad spectrum of analytical instrumentation.
• Assist in analytical method development / validation.
• Contribute to in-vitro studies and related validation activities.
• Provide support to research and development studies.
• Adhere to pharmaceutical regulatory requirements throughout the product development, QC, and stability programs.
• Assist in laboratory maintenance and calibration, GMP activities, requisitioning of materials, logistics, quality, and continuous improvement activities as required.
• Analyse laboratory investigation reports, deviations, change controls and CAPA documents in a timely manner.
• Assess data to prepare and review scientific documents and reports including SOPs, specifications, CAPEX, CoAs, methods and regulatory documentation.
• Support in vitro method development and validation activities.
  

Skills, knowledge and personal traits required for this role:
 

• The ideal candidate will have a BSc Pharmaceutical Science or Chemistry coupled with proven experience in the analysis of pharmaceutical products and the use of scientific instrumentation such as HPLC and GC.
• Demonstrated experience in GMP stability programs.
• Knowledge in the identification and troubleshooting of technical issues involving OOS or atypical test results, instrumentation, and analytical methodology.
• Ensure work is performed according to GLP / GMP standards in a timely manner without impacting quality output.

You will possess a thorough knowledge of analytical chemistry and analytical techniques coupled with excellent communication skills and hands-on capabilities. Strong organisational skills and attention to detail whilst able to multi-task and prioritise are essential.

The company offers a dynamic environment that fosters a work culture emphasising teamwork with a commitment that embodies their vision and values, celebrates diversity and thought, and supports a balance of professional and personal needs.

To submit your application in strict confidence, click the 'apply' button. If you require further information, please contact Voula Triantafillou on 03 9864 6***.