Shift Manager: Pharma Manufacturing & CI Lead

Lipa Pharmaceuticals Limited; Sydney; On-site; AUD 90,000 - 120,000; Full time

Benefits offered by this job

Onsite parking

Ongoing training and support

Rewards and Recognition Program

Job summary

Lipa Pharmaceuticals Limited is seeking an experienced Shift Manager to lead our day shift on a permanent full-time basis. You will ensure safety and quality standards are upheld while meeting daily production requirements, coaching supervisors, and building a capable team of operators.

Ideal candidates will bring leadership experience, strong communication skills, and a proactive hands-on approach to maintain GMP and SOP compliance across the site.

Qualifications

• Proven leadership experience in a manufacturing environment.
• Strong communication and problem-solving skills.
• Proficiency with Microsoft Office and ability to multitask in a dynamic setting.

Responsibilities

• Serve as the primary point of contact on shift and escalate as needed.
• Participate in risk management under WH&S and QMS systems.
• Maintain production quality and meet daily targets.
• Ensure GMP and SOP compliance in production and packing.
• Manage and develop staff on the designated shift; monitor attendance and performance.
• Maintain a safe working environment and ensure QA records are completed.
• Coordinate shift handovers to the following shift and management team.
• Support coaching, development, and performance management with the Manufacturing Manager, HR and Training teams.
• Lead CI initiatives to deliver priority process improvements.

Skills

Leadership

Communication

Problem-solving

MS Office

Job description

Lipa Pharmaceuticals Limited is seeking an experienced Shift Manager to lead our day shift on a permanent full-time basis. You will ensure safety and quality standards are upheld while meeting daily production requirements, coaching supervisors, and building a capable team of operators.

Ideal candidates will bring leadership experience, strong communication skills, and a proactive hands-on approach to maintain GMP and SOP compliance across the site.