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Scientist - Virus Validation

Employer
CSL - Australia
Location
Broadmeadows, AU
Salary
Competitive
Start date
22 Jul 2021
Closing date
9 Aug 2021

View more

Discipline
R & D , Scientific
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

With operations in 35+ nations and ~ 27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma , one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

The Opportunity:

We have an exciting opportunity available for an experienced Scientist to join the Global Pathogen Safety (GPS) team at CSL Behring, Broadmeadows.

Under the guidance of Senior Scientist/Manager, you will:

  • Participate in performing studies using blood borne human pathogens and model viruses that provide laboratory-based data and scientific support on pathogen safety related to the manufacturing of new or existing CSL Behring products.
  • Work in Department of Agriculture, Water and Environment Biosecurity Containment level 2 & 3 laboratories.
  • Assist in the implementation of Pathogen Safety strategies and objectives.
  • Ensure compliance to GLP and GMP (where applicable).
  • Assist in the preparation of Pathogen Safety study protocols and study reports.


Other Key Responsibilities Include:
  • Contribute to the development and validation of scale-down laboratory models of steps used in GMP manufacture for pathogen (virus) clearance.
  • Assist in preparation of laboratory related documentation including work instructions (WI) and standard operating procedures (SOPs).
  • Collaborate with other relevant functions across the global CSL organisation e.g., QC, Manufacturing as required.
  • Assist in solving routine Pathogen Safety issues.


Skills and Experience:

Required:
  • Tertiary qualification/degree in an appropriate scientific discipline
  • Scientific creativity, critical thinking, fast learning capabilities
  • Flexible and adaptable to rapidly developing and/or changing priorities
  • Strong verbal and written communication skills with attention to detail
  • Computer literate
  • A Team Player - actively contributes to the team by completing tasks and meeting team objectives and goals.


Preferred:
  • Established knowledge and hands-on experience with the following:
    • Scale-down-modelling of Biopharmaceutical manufacturing processes
    • Cell culture
    • Virology
    • Protein Chemistry or another related specialised disciplines.
  • Understanding of the principles of GMP, GLP and of laboratory safety


How to Apply:

Applications must address the selection criteria above and include a current CV and covering letter.

Applications 8 August 2021.

Employment screening, including criminal history, medical assessment, confirmation of experience and stated qualifications, Australian working rights and other relevant checks form part of the candidate suitability

Worker Type:
Employee

Worker Sub Type:
Regular

Company

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