Senior Scientist QC Instrumentation Standards

2 weeks ago


Broadmeadows, Victoria, Australia CSL Full time

At CSL Behring, we are committed to saving lives through the development of innovative biotherapeutics.

As a key player in our global QC digitalization strategy, you will be responsible for delivering a Laboratory Execution System that enables seamless digital workflows in QC.

In this role, you will collaborate with our QC teams across the globe to establish a standardized global process for laboratory automation, ensuring consistency and efficiency in our testing processes.

Your primary objective will be to create digital workflows based on analytical method SOPs and process maps, utilizing the Laboratory Execution System BIOVIA ONE Lab, and maintain the life cycle of these workflows as a subject matter expert.

You will also be responsible for supporting laboratory instrumentation standardization projects and global data integrity initiatives, ensuring compliance with regulatory requirements.

With a strong background in a relevant scientific discipline and experience in laboratory automation, you will possess excellent written and verbal communication skills, with the ability to collaborate with teams locally and globally.

We are looking for a highly motivated and analytical individual who can drive progress forward, making informed decisions and contributing to the growth and success of our organization.

Key Responsibilities:

  • Create digital workflows based on analytical method SOPs and process maps.
  • Establish process documents to support implementation of a global Laboratory Execution System for QC.
  • Support QC business processes standardization efforts around laboratory automation.
  • Maintain the life cycle of digital workflows as a subject matter expert.
  • Support laboratory instrumentation standardization projects and global data integrity projects.

Requirements:

  • University degree in a relevant scientific discipline (Biology, Chemistry, Microbiology, etc.).
  • 3-5 years' experience in a pharmaceutical/medicinal GMP testing environment using a variety of testing instrumentation, experience in instrument lifecycle activities and data integrity.
  • Minimum 2 years' experience with laboratory automation in QC or R&D.
  • Knowledge of the software BIOVIA ONE Lab or similar systems is a benefit.
  • Knowledge of regulations on computerized systems and laboratory automation and willingness to extend skills and know-how on the field.

Our Benefits

We prioritize your well-being and encourage you to make it a priority. Your health and happiness are important to us.



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