Your new company

Your new role

This role reports to the quality manager and will be a part of a team to provide quality support in compliance with GMP and GLP requirements from starting materials to finished goods. Your role will include, not limited to, Ensuring compliance with SOP's, Maintaining continuous improvement and maintaining QMS. You will work closely with other business units such as regulatory affairs and validation. You will be responsible for reviewing and approving change controls, deviations, investigations, CAPA's and performing internal and external audits. You will support batch release activities and review of GMP AND non-GMP activities.

What you'll need to succeed

• Tertiary qualified in science related field

• Experience working in Quality Assurance in pharmaceuticals, medical devices or biotech setting

• Advanced knowledge of TGA, FDA, EMA

• Excellent communication skills

Proficient with computer skills

What you'll get in return

This company is a growing organisation with an excellent reputation on the market. The company offers an excellent work-life balance and a 9-day fortnight. The company offers an excellent salary package, including up to 10% bonus and an employee share plan.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.