About the Company & Role: Join a
Leading Veterinary Pharmaceutical Company who specialize 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 collaborative 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.
Apply Now!Ready to take the next step in your career?
Submit your application today! Please include a
detailed resume in Word format (PDFs may not process correctly)
For any questions about the role, contact
Mairead on +61 2 8071 4290.
With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.