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

Strong 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.