Company

Bayside GroupSee more

addressAddressMelbourne, VIC
CategoryIT

Job description

  • 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***.

Refer code: 2242685. Bayside Group - The previous day - 2024-05-23 01:15

Bayside Group

Melbourne, VIC
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