GMP CQV Engineer: Commissioning & Validation Lead

biotech

City of Melbourne

On-site

AUD 120,000 - 180,000

Full time

14 days+
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Job summary

biotech seeks a C&Q Engineer to ensure GMP systems, facilities, and equipment meet design requirements for a new Melbourne facility.

You will plan, coordinate and execute commissioning, qualification and validation activities (DQ, FAT, SAT, IQ, OQ, PQ, PV), develop protocols and final reports, and support project teams across Engineering, Quality, Manufacturing and Project Management. You will mentor colleagues and ensure cGMP compliance and timely delivery.

Qualifications

  • 5+ years of experience in pharmaceutical/biotech/GMP environments.
  • Experience applying a risk-based CQV approach.
  • Proficient in authoring and executing DQ, FAT, IQ, OQ, PQ, and PV documents.
  • Proficient in developing SOPs, final reports and validation & quality policies.
  • Experience with CQV procedures and policies.

Responsibilities

  • Plan, coordinate, and execute commissioning, qualification and validation activities for GMP systems and equipment.
  • Develop and review qualification protocols, test documentation, and validation reports.
  • Write and revise GMP and GDP documents and technical specifications.
  • Support FAT, SAT, commissioning and qualification activities throughout the project lifecycle.
  • Develop SOPs and review final reports; mentor and consult to client and local team.

Skills

CQV knowledge
GMP experience
Project coordination
Documentation skills

Education

Bachelor's degree in Engineering/Science

Tools

Kaye Validator
Testo
Kneat

Job description

biotech seeks a C&Q Engineer to ensure GMP systems, facilities, and equipment meet design requirements for a new Melbourne facility.

You will plan, coordinate and execute commissioning, qualification and validation activities (DQ, FAT, SAT, IQ, OQ, PQ, PV), develop protocols and final reports, and support project teams across Engineering, Quality, Manufacturing and Project Management. You will mentor colleagues and ensure cGMP compliance and timely delivery.

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