We are seeking experienced Production Technicians to support the safe, compliant, and efficient manufacture of therapeutic plasma products in Turner Filling facility. This role is responsible for executing aseptic filling operations, maintaining GMP compliance, troubleshooting equipment and process issues, training team members, and contributing to continuous improvement initiatives.
The successful candidate will work both independently and collaboratively to ensure production schedules, quality requirements, and operational targets are achieved. Our facility currently operates on a 24-hour, 5.5-day (S-F). Shift patterns may evolve, and we are seeking operators who are flexible and willing to work across all shifts, including weekends if required.
Day Shift: 6:30am – 2:21pm Afternoon Shift: 1:30pm – 9:21pm Night Shift A: 9:00pm – 4:51am Night Shift B: 11:30pm – 7:21am
Permanent/Fixed term opportunity, multiple positions available. These roles involve regular manual handling, prolonged periods of standing, and repetitive physical tasks.
Key Responsibilities
Perform aseptic filling operations, line setup, interventions, equipment changeovers, and cleaning activities in accordance with GMP requirements and approved batch documentation.
Operate, monitor, troubleshoot, and optimize filling equipment to support production schedules and manufacturing targets.
Complete batch records, logbooks, environmental monitoring, filter integrity testing, and inventory activities accurately and in a timely manner.
Lead troubleshooting efforts and support deviation investigations, CAPAs, root cause analysis, and continuous improvement initiatives.
Train, mentor, and provide technical guidance to team members while acting as a subject matter expert for aseptic filling operations.
Collaborate with Quality, Engineering, Validation, Planning, and other internal stakeholders to deliver manufacturing objectives safely, compliantly, and on schedule.
Experience & Qualifications
Experience working in aseptic processing, sterile manufacturing, or pharmaceutical production environments.
Demonstrated knowledge of GMP/cGMP requirements and controlled manufacturing processes.
Strong technical capability in manufacturing operations, equipment troubleshooting, and quality systems.
Experience within the pharmaceutical, biotechnology, medical device, or another regulated manufacturing industry.
Excellent communication and stakeholder management skills with the ability to work independently and as part of a team.
Tertiary qualification in Science, Engineering, or a related discipline preferred, or equivalent industry experience.
How to Apply
Please submit your application, including your CV, as a single document.
