At a Glance
- Tasks: Support process validation and ensure compliance in a dynamic pharmaceutical manufacturing environment.
- Company: Join a leading veterinary pharmaceutical company focused on innovation and excellence.
- Benefits: Gain valuable experience in a regulated environment with potential for career growth.
- Other info: Exciting contract role with opportunities to collaborate across teams.
- Why this job: Be part of a team making a real difference in veterinary medicine.
- Qualifications: Bachelor's degree in Science or Engineering and 3+ years in a regulated manufacturing setting.
The predicted salary is between 67500 - 82500 $ per year.
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
Manufacturing Scientist in Rutherford employer: Evolve Scientific
Join a leading pharmaceutical company in the Southeast suburbs of Melbourne, where you will be part of a dynamic team dedicated to quality and compliance. With a strong focus on employee development and a culture that promotes continuous improvement, this role offers meaningful opportunities for growth in a supportive environment. Enjoy the benefits of full-time hours, a collaborative work culture, and the chance to make a significant impact in the pharmaceutical industry.
