CQV Engineer II: Commissioning & Validation Lead in Melbourne

CQV Engineer II: Commissioning & Validation Lead in Melbourne

Melbourne Full-Time 72000 - 88000 $ / year (est.) On-site
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At a Glance

  • Tasks: Lead commissioning and validation projects while ensuring compliance with industry standards.
  • Company: PSC Biotech, a leader in biotech solutions based in Melbourne.
  • Benefits: Competitive salary, growth opportunities, and a collaborative work environment.
  • Other info: Exciting travel opportunities and dynamic project involvement.
  • Why this job: Join a mission-driven team making a real impact in the biotech industry.
  • Qualifications: Experience in CQV processes and strong teamwork skills required.

The predicted salary is between 72000 - 88000 $ per year.

PSC Biotech in Melbourne, Australia is seeking a CQV Engineer II to support commissioning, qualification, and validation of facilities and equipment.

The role emphasizes maintaining design intent while enabling steady growth and development within the PSC mission.

The candidate will author controlled CQV documents, coordinate risk analyses, and collaborate across departments.

Travel may be required as projects demand, with a focus on ensuring c GMP/Data Integrity compliance.

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CQV Engineer II: Commissioning & Validation Lead in Melbourne employer: PSC Biotech

As a Senior Process Engineer in Melbourne, you'll join a dynamic team dedicated to innovation in the pharmaceutical sector. Our company fosters a collaborative work culture that prioritises employee growth through continuous learning and development opportunities, while also offering competitive benefits and a commitment to compliance and quality. With a focus on operational excellence and cutting-edge technology, we provide a rewarding environment where your expertise will directly contribute to impactful projects.

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Contact Details:

PSC Biotech Recruitment Team

We think you need these skills to ace CQV Engineer II: Commissioning & Validation Lead in Melbourne

Commissioning
Qualification
Validation
CQV Documentation
Risk Analysis
cGMP Compliance
Data Integrity