Permanent GMP Validation Specialist – Sterile QA in Melbourne

Permanent GMP Validation Specialist – Sterile QA in Melbourne

Melbourne Full-Time 75600 - 92400 $ / year (est.) On-site
E

At a Glance

  • Tasks: Plan and execute qualification activities in a GMP-regulated environment.
  • Company: Evolve Scientific, a leader in pharmaceutical quality assurance.
  • Benefits: Full-time role with competitive salary and growth opportunities.
  • Other info: Located in Melbourne's southeast suburbs, excellent communication skills required.
  • Why this job: Join a dynamic team and make a real impact in pharma manufacturing.
  • Qualifications: Minimum 3 years in pharma manufacturing with strong sterile processing experience.

The predicted salary is between 75600 - 92400 $ per year.

Evolve Scientific seeks a qualified professional to plan and execute qualification activities in a GMP-regulated environment.

You will develop, review and approve validation documentation for facilities, equipment and processes, including IQ/OQ/PQ, while supporting audits and continuous improvement.

Based in Melbourne's southeast suburbs, this full-time role requires a minimum of 3 years in pharma manufacturing, with strong sterile processing experience and excellent communication skills.

Permanent GMP Validation Specialist – Sterile QA in Melbourne employer: Evolve Scientific

Join a leading pharmaceutical company in the Southeast suburbs of Melbourne, where you will be part of a dynamic team dedicated to quality and compliance. With a strong focus on employee development and a culture that promotes continuous improvement, this role offers meaningful opportunities for growth in a supportive environment. Enjoy the benefits of full-time hours, a collaborative work culture, and the chance to make a significant impact in the pharmaceutical industry.

E

Contact Details:

Evolve Scientific Recruitment Team

We think you need these skills to ace Permanent GMP Validation Specialist – Sterile QA in Melbourne

GMP Knowledge
Validation Documentation Development
IQ/OQ/PQ Execution
Sterile Processing Experience
Audit Support
Continuous Improvement
Pharmaceutical Manufacturing Experience