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QC Analytical Technology Analyst x 2

2 x QC Analytical Technology Analyst – 1x Biochemistry, 1 x Chemistry

Please see individual job descriptions below:

Job Title: QC Analytical Technology Analyst (Chemistry)
Start/End Dates: 15/01/2024 – 14/01/2025
Worker Location: CSL Limited Australia-Broadmeadows
Job Description:
We are looking for a talented QC Analytical Technology Analyst (Chemistry) to join our team at CSL Limited Australia-Broadmeadows. As a key contributor to our Quality team, you will be pivotal in the development, optimization, and validation of methods, with a focus on the upcoming creation of a site in Tullamarine and the decommissioning of the Parkville site. This role involves the transition of methods from Parkville to Broadmeadows, making it an exciting and impactful opportunity.

High-Level Project Details:
The primary project involves the creation of a site in Tullamarine, with the concurrent decommissioning of the Parkville site. Methods currently in use at Parkville will be transitioned to Broadmeadows, requiring a meticulous and detail-oriented QC Analytical Technology Analyst to ensure a smooth and successful transition.

Must-haves:
* Minimum 3 years of experience in a QC or method validation environment.
* Experience in Chromatography (LC, GC), Spectroscopy (AAS, UV, Raman), Titrimetry, Direct Instrumental Measurements (pH, Conductivity, Density, Osmolality), and Nitrogen Determination by Combustion.

Role:
* This role involves more bench work than the more senior positions.
* Experimental studies for the development, optimization, and validation of methods.
* Execution of method transfers between CSL sites/areas and external laboratories.
* Implementation of methods and innovative technologies.
* Participation in remediating analytical challenges within CSL’s Chemistry laboratory.
* Support in the preparation, review, and update of standard operating procedures, test procedures, protocols, reports, and associated documentation in the performance of QCAT studies and investigations, following CSL’s documentation and data integrity requirements.
* On-track achievement of project deliverables through collaboration, under the general guidance of the Head of QCAT or delegate.
* Contribution to the knowledge and practical execution of studies during the investigation of deviations, atypical results, and method performance issues.
* Providing colleagues with technical assistance, scientific support, and training as required.

Location: Broadmeadows
Team Size: 12 employees, plus 7 CWs, plus 10-15 others in execution of the role.
Flexibility: No, this role is all onsite.
Hours: 38 hrs per week, standard Mon to Fri, 9 am to 5 pm.
Overtime: If the person works more than 38 hours in the week, approval is required, and penalty rates for overtime are applicable.
Potential to Extend: Too early to say.
Reports to: Head of QCAT Multifunctional Lead
Additional Information:
* Candidates must have sufficient work rights to work in the position for a minimum of 12 months.




Job Title: QC Analytical Technology Analyst (Biochemistry)
Position Title: QC Analytical Technology Analyst (Biochemistry)
Start Date: 15/1/2024
End Date: 12 months
Minimum Education: Bachelor’s Degree in Biochemistry and Molecular Biology or in a relevant scientific discipline (Biology, Chemistry, etc.)

Job Description: We are seeking a dedicated Analyst to join CSL Behring’s Quality Control Analytical Technologies (QCAT) Biochemistry team at the Broadmeadows site in Australia. Reporting to the Head of QCAT, you will play a vital role in ensuring the efficient and safe execution of Biochemistry testing in alignment with approved test protocols, procedures, and adherence to the Code of Good Manufacturing Practice and data integrity principles.
High-Level Project Information: Creation of a site in Tullamarine, Parkville site to be decommissioned. Methods in Parkville will be transitioned to Broadmeadows.

Must Haves:
* Bachelor’s Degree in Biochemistry and Molecular Biology or in a relevant scientific discipline (Biology, Chemistry, etc.).
* Experience in cGMP Quality Control in pharmaceutical, biotechnology, or related industry a plus.
* Experience in ELISA, Electrophoresis, or Endotoxin testing a plus.
Role: More bench work than the senior roles. Reporting to the Head of QCAT, responsible for ensuring that all Biochemistry testing is efficiently and safely carried out in accordance with approved test protocols, procedures, and in accordance with the Code of Good Manufacturing Practice and data integrity principles.
* Ability to manage timelines to ensure testing and activities are completed in a timely manner.
* Performing biochemical testing for routine and/or method validation (e.g., ELISAs, Immunodiffusion, Electrophoresis, Endotoxin).
* Ensure efficient, precise, and accurate reporting of test results according to data integrity principles.
* Ensure equipment and facilities are maintained/prepared in accordance with approved procedures.
* Participate in the investigation of out-of-specification and invalid results as required.
* Assist with the preparation, review, and update of documentation related to testing such as protocols, reports, and standard operating procedures.
* Complete other duties assigned by the reporting manager or delegate.

Location: Broadmeadows
Team Size: 12 employees, plus 7 CWs, plus 10-15 others in the execution of the role.
Flexibility: No, this role is all onsite.
Hours: 38 hrs per week, standard Mon to Fri, 9 am to 5 pm.
Overtime: If the person works more than 38 hours in the week, approval is required, and penalty rates for overtime are applicable.
Potential to Extend: Too early to say.
Reports to: Head of QCAT

Additional Information:
* Candidates must have sufficient work rights to work in the position for a minimum of 12 months.

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