Pharma Process Validation Specialist (Contract)

Evolve Scientific; Rutherford; On-site; AUD 85,000 - 110,000; Full time

Job summary

Evolve Scientific – Rutherford NSW is partnering with a leading veterinary pharmaceutical company to appoint a Process Validation Specialist for an initial 4-month contract. You will join the Validation team to support process validation, cleaning validation and media fill activities in a GMP-compliant manufacturing environment, with a strong emphasis on documentation.

The role focuses on authoring validation protocols and reports, analysing validation data, reviewing batch documentation, and

Qualifications

• Bachelor's degree in science/engineering or related field.
• 3+ years' experience in pharmaceutical/biopharmaceutical manufacturing.
• Direct GMP validation experience.
• Experience authoring validation protocols and reports.

Responsibilities

• Author and review process validation protocols and reports
• Support process validation, cleaning validation and media fill activities
• Analyse validation data and prepare technical reports
• Review batch and manufacturing documentation
• Ensure validation protocols are executed per requirements
• Coordinate sample collection and validation activities
• Liaise with Production teams on validation planning and execution
• Liaise with Quality teams to support GMP compliance and document approval
• Support new product introduction activities
• Assist with validation-related deviations, investigations and CAPAs
• Support process improvement initiatives and manufacturing operations

Skills

Validation protocols

GMP compliance

Documentation

Cross-functional teamwork

Data analysis

Education

Bachelor's degree in science/engineering

Job description

Evolve Scientific – Rutherford NSW is partnering with a leading veterinary pharmaceutical company to appoint a Process Validation Specialist for an initial 4-month contract. You will join the Validation team to support process validation, cleaning validation and media fill activities in a GMP-compliant manufacturing environment, with a strong emphasis on documentation.

The role focuses on authoring validation protocols and reports, analysing validation data, reviewing batch documentation, and