Production Supervisor

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.