At a Glance
- Tasks: Validate and qualify equipment and systems in a dynamic pharmaceutical environment.
- Company: Leading pharmaceutical manufacturer based in Brisbane's western suburbs.
- Benefits: Casual ongoing role with 38 hours per week, Monday to Friday.
- Other info: Opportunity for growth in a GMP-regulated environment with a focus on continuous improvement.
- Why this job: Join a team making a real difference in healthcare through innovative validation processes.
- Qualifications: Bachelor's degree in Engineering or Science and hands-on validation experience.
The predicted salary is between 58500 - 71500 $ per year.
About the Role
Our client, a leading pharmaceutical manufacturing company based in Brisbane's western suburbs, is seeking an experienced Validation Engineer to join their team on a casual ongoing basis for 6-12 months, working Monday to Friday, 38 hours per week.
This role will support validation and qualification activities across maintenance/Engineering, Production and Packaging, providing technical expertise for equipment, facilities and systems within a GMP-regulated manufacturing environment.
Applicants will be required to successfully complete a medical assessment, drug screening and police check.
Key Responsibilities
- Execute equipment, facility and system validation and qualification activities.
- Develop and execute validation documentation, including URS, FS, Risk Assessments, IQ, OQ, PQ and validation reports.
- Support new equipment/system installations, upgrades and lifecycle management.
- Provide technical support for equipment changes and risk-based change management.
- Investigate and report deviations and support Continuous Improvement initiatives.
- Ensure activities comply with GMP/c GMP, company procedures and health and safety requirements.
Skills & Experience
The successful candidate will have
- A Bachelor's degree in Engineering, Science or a related discipline.
- Hands-on experience with equipment, facility and/or system validation and qualification.
- Experience with validation lifecycle documentation such as URS, FS, DS, IQ, OQ, PQ and Traceability Matrices.
- Experience working in a GMP manufacturing or highly regulated environment.
- Understanding of risk-based change management/change control.
- Strong technical writing, communication and organisational skills.
- Experience in Manufacturing and working with Project Management Systems.
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Validation Engineer 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.
