Process Validation Specialist (Pharmaceutical Manufacturing)
About the Company & Role: Join aLeading Veterinary Pharmaceutical Companywho specialise in the development and manufacturing of veterinary medicines.
This is your chance to be part of a team committed to excellence and innovation.
An exciting opportunity is available for aProcess Validation Specialistto join their Rutherford manufacturing facility on an initial 4-month contract.
Working within the Validation team, you will support process validation, cleaning validation and media fill activities while ensuring compliance with GMP requirements.
This is a documentation-focused role suited to candidates with experience authoring validation protocols and reports, analysing validation data, reviewing batch documentation and collaborating with Quality and Production teams within a regulated manufacturing environment.
Duties:
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 in accordance with requirements
Coordinate sample collection and validation activities
Liaise with Production teams regarding 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 as required
Skills & Experience:
Bachelor's Degree in Science, Chemical Engineering, Industrial Engineering or a related discipline
3+ years' experience within pharmaceutical, biopharmaceutical, consumer healthcare or cosmetics manufacturing environments
Direct validation experience within a regulated GMP environment
Experience authoring validation protocols and validation reports
Strong data analysis and technical documentation skills
Experience reviewing batch documentation and manufacturing records
Understanding of pharmaceutical quality systems and GMP requirements
Experience with Minitab, SAP, ETS, Viva document control systems - highly regarded
Experience with synthetic chemical manufacturing processes - highly regarded
Strong communication and stakeholder engagement skills
Ability to work autonomously and manage multiple priorities
Culture & Benefits:
Free on-site parking for your convenience
Be part of a collaborative and experienced technical team
Work closely with Validation, Production and Quality professionals
Gain exposure to a globally recognised veterinary pharmaceutical manufacturer
Supportive team setting with strong technical leadership
Please Note:
A police check and pre-employment medical (including drug and alcohol screening) are required prior to commencement.
These will be organised by the company.
#J-*****-Ljbffr

📌 Process Validation Specialist (Pharmaceutical Manufacturing) (New South Wales)
🏢 Evolve Scientific
📍 New South Wales