AddressWe are hiring for Bulk Technicians (Two positions available) in AlbuRx Bulk value stream for our manufacturing Broadmeadows site.
The role of the AlbuRx Bulk Technician exists to execute daily manufacturing process operations under the supervision of the Bulk Supervisor and Team Leader in a safe, GMP compliant and cost-efficient manner. The Technician is required to follow the established procedures and methods of manufacture so that products of the right quality (meeting specification) are produced, at the right cost of goods, in the correct quantity (yield) and process cycle time so the requirements of the detailed weekly Manufacturing Schedule are met. Support the Bulk Team in following a standard work protocol so the team operates every element of the process in the same way, every time.
This is a permanent opportunity initially working day shift during the project phase. Potential shift work may be required during operations phase. There could be occasional overtime work so flexibility is required across the team. At the conclusion of the project phase, the role will be merged into the existing operations team. Morning and afternoon shift work will be required during the operation phase of the role.
The Role:
Project Phase:
- Deliver on the project timelines and provide subject matter expertise about processes
- Develop processes and procedures for equipment operation including troubleshooting
- Participate in commissioning and qualification activities
- Operate the automation system to enable testing of the newly developed processes and installed equipment
- Develop and execute water trials to test processes
- Work with the existing routine operations team to ensure a successful integration
- Ensure the AlbuRx Bulk process for the engineering and validation batches is delivered as per the project timelines
- Perform (where required), appropriate training for AlbuRx Bulk staff prior to validation activities
Operational Phase:
- Ensure that all AlbuRx manufacturing environments operate according to the principles of cGMP as required by relevant regulatory agencies and standards.
- Ensure all production activities are performed in line with manufacturing procedures and as directed by the Bulk Supervisor or Team Leader.
- Perform production activities so the weekly schedule of activities is met in a cost efficient and consistent manner. Ensure that agreed and scheduled time points are met consistently and notify the Bulk Supervisor or Team Leader as early as possible if there is any risk of the schedule not being met.
- Safeguard the health, safety, and security of the AlbuRx Bulk personnel during the validation of the facility.
- Provide timely input into investigation and closeout of manufacturing deviations and CAPA’s for the AlbuRx Bulk area.
To be successful:
- A tertiary qualification in science/engineering or related discipline is desirable but not essential.
- Experience working in a busy dynamic environment.
- Experience working in a strict process focussed environment.
- A team player with proven problem-solving, demonstrated initiative and good communication skills.
- Demonstrated ability to co-ordinate project activities and liaise across functional groups to meet project targets and objectives.
Apply now to join a growing business in a great team environment.
Please include a CV and Cover Letter in your application. Applications close 5pm AEST on 14 July 2024.
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About CSL Behring
CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.
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