QC Analyst

We are looking for a Laboratory Analyst to join our Quality Control, Products of National Significance (PNS) team on a full time, permanent basis at our Woodend site. You will support the teams within the Quality Control (QC) Group to enable testing of product in accordance with the code of Good Manufacturing Practice (GMP).

This is a permanent opportunity based at our Woodend site and will require to work day, afternoon and night rotational shifts including weekends.

Reporting to the QC Team Leader, you will:

• Support the team to ensure that the biological and non-biological assays performed in each department are prepared and executed in accordance with the code of Good Manufacturing Practice (cGMP)
• Assist in the review, update, and issue of documentation.
• Assist with investigations of Out-of-Specification (OOS) test results, invalid assays or when unusual data is observed as required.
• Ensure testing is conducted in accordance with the approved procedures. Ensures containers/materials/samples/products are stored and labelled according to specifications completing all necessary documentation.
• Use LIMS for data entry of quality control testing results and maintaining laboratory equipment calibration and cleaning.
• Support the operational area pro-actively to prevent invalid assays and reduce out of specification results.
• Support the validation and maintenance systems of an operational area to ensure plant, equipment and processes is available as required.
• Actively seek, recommend, and implement improvements to enhance quality within each functional area.

Experience:

• Bachelor's degree in a relevant scientific discipline (e.g., Biology, Chemistry, Biochemistry, or related field).
• Previous experience working with animals is desirable.
• Previous experience in a similar Quality Control environment and strong knowledge on Good Manufacturing Practice (GMP) regulations and guidelines.
• Proficiency in laboratory techniques including assay preparation and execution.
• Experience with Laboratory Information Management Systems (LIMS) for data entry and management.
• Flexible to work on rotational shifts including day, afternoon and night shift work and weekends.
• During the first 12 months, working from other locations as required, including Tullamarine.
• Ability to work on your own

About CSL Seqirus

CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

 To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

Watch our ‘On the Front Line’ video to learn more about CSL Seqirus