Process Validation Specialist (Pharmaceutical Manufacturing)

About the Company & Role: Join a Leading Veterinary Pharmaceutical Company who 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 a Process Validation Specialist to 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 cooperative and experienced technical team
- Work closely with Validation, Production and Quality professionals
- Gain exposure to a globally recognised veterinary pharmaceutical manufacturer
- Supportive team environment 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.

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📌 Process Validation Specialist (Pharmaceutical Manufacturing) (Rutherford)
🏢 Evolve Scientific
📍 Rutherford