Based in the Southeast suburbs of Melbourne Monday to Friday, full time hours Plan, coordinate, execute, review, and approve qualification and validation activities Develop, review, and approve qualification and validation documentation, including protocols, reports, risk assessments, validation plans, and associated records. Perform qualification activities for facilities, utilities, equipment, and computerized systems, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) Participate in the management of quality system processes, including deviations, investigations, CAPAs, change controls, and risk assessments Support the development, review, and maintenance of quality and validation procedures Support internal audits, customer audits, and regulatory inspections Identify opportunities to improve quality systems, validation processes, and ways of working. Promote a culture of quality, compliance, continuous improvement, and inspection readiness throughout the organisation

About you:

Tertiary education in Science, Engineering or Pharmaceutical Science Minimum of 3 years’ experience working within a GMP-regulated pharmaceutical,complementary medicines, nutraceutical, medical device, or other regulated manufacturing setting Must have strong experience in sterile processing and pharmaceutical manufacturing Problem solving, creative thinking, and effective decision-making skills Excellent communication skills, detail oriented and team collaboration. Experience with qualification and validation of facilities, utilities, equipment,processes, cleaning programs, and/or computerized systems bout the role:





Pharmaceutical company Based in the Southeast suburbs of Melbourne Permanent Opportunity Monday to Friday, full time hours About your duties:

Plan, coordinate, execute, review, and approve qualification and validation activities Develop, review, and approve qualification and validation documentation, including protocols, reports, risk assessments, validation plans, and associated records. Perform qualification activities for facilities, utilities, equipment, and computerized systems, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) Participate in the management of quality system processes, including deviations, investigations, CAPAs, change controls, and risk assessments Support the development, review, and maintenance of quality and validation procedures Support internal audits, customer audits, and regulatory inspections Identify opportunities to improve quality systems, validation processes, and ways of working. Promote a culture of quality, compliance, continuous improvement, and inspection readiness throughout the organisation

About you:

Tertiary education in Science, Engineering or Pharmaceutical Science Minimum of 3 years’ experience working within a GMP-regulated pharmaceutical,complementary medicines, nutraceutical, medical device, or other regulated manufacturing environment Must have strong experience in sterile processing and pharmaceutical manufacturing Problem solving, creative thinking, and effective decision-making skills Excellent communication skills, detail oriented and team collaboration. Experience with qualification and validation of facilities, utilities, equipment,processes, cleaning programs, and/or computerized systems

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📌 Quality Validation Associate (Port Phillip City)
🏢 Evolve Scientific
📍 Port Phillip City