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 organisationAbout 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 workplace
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 organisationAbout 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 (Melbourne)
🏢 Evolve Scientific
📍 Melbourne