LOCATION
Rosedale, SA

About the Company/Role

Our client is a global specialty pharmaceutical company focused on life-saving medicines and critical care treatments. Reporting to the Operations Manager, you will be responsible for supervising Cleanroom operations, ensuring compliance with cGMP standards, supporting low-bioburden serum production, and driving operational excellence through continuous improvement initiatives. You will lead a team of Cleanroom Technicians while maintaining the highest standards of quality, safety, and efficiency.

Responsibilities include:

- Lead cleanroom technicians to achieve production and compliance objectives

- Supervise day-to-day cleanroom manufacturing activities to meet production schedules and business requirements

- Review and oversee Batch Manufacturing Records, SOPs, Quality Records, and related documentation

- Drive Continuous Improvement initiatives using Lean and Six Sigma methodologies

- Coordinate training plans and competency development programs for Cleanroom personnel

- Manage equipment validation, calibration, maintenance schedules, and associated compliance activities

- Conduct investigations, corrective actions, and root cause analysis activities as required

- Collaborate closely with Quality, Supply Chain, Engineering, and other site functions to achieve operational goals





- Contribute to site leadership initiatives and broader operational strategy as a key member of the leadership team

Skills/Experience:

- Tertiary qualifications in a scientific or technical discipline preferred

- Experience in a supervisory or team leadership role within manufacturing

- Extensive manufacturing experience in pharmaceutical, biotech, chemical, food, or similarly regulated industries

- Robust knowledge of cGMP requirements and quality management systems

- Experience leading teams in cleanroom or regulated production environments

- Demonstrated success driving continuous improvement and operational efficiency programs

- Strong problem-solving, investigation, and root cause analysis skills

- Proven ability to manage documentation, compliance activities, and production reporting

- Excellent communication and stakeholder management skills

- Strong organisational skills with the ability to prioritise in a fast-paced manufacturing environment

What’s On Offer

- Competitive salary package

- Opportunity to lead a critical GMP manufacturing function

- Strong focus on employee development and continuous improvement

- Exposure to a highly regulated and technically advanced manufacturing environment

TO APPLY:
If you would like to discuss this vacancy further, please call Nikita on (02) •••• •843 or email ••••@i-pharmconsulting.com.

📌 Production Supervisor (Adelaide)
🏢 i-Pharm Consulting Australia
📍 Adelaide