Validation Associate - 6 month contract

Validation Associate - 6 month contract

Salary:

$60 - 70 / Hour

Contract Type:

Contract

Location:

Melbourne - VIC 

Industry:

Manufacturing

Reference:

3999219

Contact Name:

Kitty Whitehead

Contact Email:

kwhitehead@designandbuild.com.au

Date Published:

14-Jan-2026

Validation Associate – 6 Month Contract

Mulgrave | Immediate Start | Potential to Extend

Are you an experienced Validation or Qualification professional looking for a hands-on contract role within a regulated pharmaceutical environment?

Do you want to step into a site-based role where you can add immediate value across qualification, requalification, and project validation activities?

On offer is a 6-month contract with the potential to extend, supporting facility, equipment, and services qualification activities across a complex pharmaceutical manufacturing site. You’ll work closely with Engineering, Quality, and Operations while contributing to both routine requalification programs and active project work.

This organisation operates within a highly regulated pharmaceutical environment and maintains strong standards around safety, compliance, and documentation. Due to increased site activity, they are seeking someone available for an immediate start who can operate autonomously and integrate quickly into the technical services function.

The Role:
  • Plan, manage, perform, and report on facility, equipment, and services qualification activities
  • Execute routine scheduled requalification and project-based validation tasks in line with site procedures
  • Maintain and update validation documentation to meet regulatory and internal requirements
  • Perform technical assessments to support site validation and qualification activities
  • Ensure smooth transition from qualification into ongoing requalification programs
  • Assist the Technical Services Manager with tools and reporting for team task tracking
Quality & Compliance:
  • Support the definition, management, and successful delivery of projects and programs
  • Ensure all work is completed in full compliance with quality systems, policies, and procedures
  • Maintain compliance with personal training requirements relating to quality systems

The Person:
  • Background in validation and qualification activities within a regulated environment
  • Strong documentation and technical report-writing capability
  • Sound understanding of cGMP requirements for equipment and systems
  • Able to work independently, manage competing priorities, and meet deadlines
  • Familiarity with pharmaceutical water systems is highly regarded
  • Available for an immediate start
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