In-Demand Process engineer Jobs

Graduate Validation & Testing Engineer
LivaNova —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
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Process Engineer (USP)
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- Weekend availability
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Egis Group —Brisbane QLD
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Quick Apply
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Senior Process Engineer – Water Treatment
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PharmaCare Group —Prestons NSW
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Quick Apply
2d
System Process Methods & Tools Engineer
Thales —Melbourne VIC
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Chemical/Process Engineer - Project Coordinator
GR Production Services Pty Ltd —Brisbane QLD
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Quick Apply
Professional / Senior Process Engineer - Water Infrastructure
AECOM —Brisbane QLD
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Arrow Energy —Brisbane QLD
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Principal Process Engineer - Resources Consulting
Worley —Brisbane QLD
- Full-time
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9d
Data Engineer
Infosys Singapore & Australia —Melbourne VIC
- Full-time
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Quick Apply
10d
GHD Graduate Program 2026/27 - WA - Process Engineers
GHD —Perth WA
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2d
Senior Process Engineer
Peabody Energy —Glenden QLD
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Senior / Principal Process Engineer (Wastewater)
Stantec —Melbourne VIC
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Senior Process Safety & Risk Engineer
Ampol —Lytton QLD
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Senior Process Engineer
Ausenco —Perth WA
- Full-time
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- Work from home
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Senior Engineer - Process Engineering
Water Corporation —Leederville WA
- From $135,693 a year
- Remote
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- Annual leave
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1d

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Graduate Validation & Testing Engineer

LivaNova -
Melbourne VIC

Apply Now

Job Details

Full-time

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Technical drawing
Engineering
Microsoft Office
Analysis skills
Communication skills

Full Job Description

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.

Job Summary

This role will support the engineering department with component validation and testing, preparing technical protocols and reports, maintaining engineering documentation, and collaborating with cross-functional teams to ensure compliance with regulatory and quality requirements.

This role sits within the Engineering Department and would suit a detail-oriented graduate or early-career engineer/scientist with a strong interest in medical devices, product validation, and quality systems.

Key Responsibilities

Validation, Verification & Testing

Conduct component verification and validation testing to ensure compliance with quality, performance, and regulatory requirements.
Perform physical, functional, and integrity testing of components and assemblies.
Develop, execute, and document test protocols and validation activities.
Support the development, verification, and continuous improvement of test methods.
Review, document, and assess biological and physical characteristics of materials and components.
Support validation and verification activities in accordance with applicable medical device regulatory requirements, including ISO 13485, ISO 14971, and relevant internal procedures.
Ensure testing activities are conducted and documented in compliance with quality management system requirements.
Analyse test data, identify trends, and prepare technical reports with conclusions and recommendations.
Investigate test failures and support root cause analysis activities.
Support component and material qualification activities, including supplier change assessments and material evaluations.
Assist in the review of material specifications, certifications, and technical documentation.

Sample Preparation & Cross-Functional Collaboration

Participate in sample preparation and testing activities within controlled cleanroom environments.
Collaborate with Engineering and Quality teams to facilitate routine product monitoring and testing.
Support manufacturing and process engineering activities related to product development, validation, and continuous improvement initiatives.
Adhere to cleanroom procedures, Good Manufacturing Practices (GMP), and safety requirements at all times.
Participate in process improvement initiatives to enhance product quality, efficiency, and compliance.
Assist with laboratory and testing activities as required.

Documentation & Quality Support

Create, maintain, and review material specifications.
Support risk management activities, including risk assessments, hazard identification, risk analysis, and maintenance of risk management documentation in accordance with ISO 14971.
Archive and maintain engineering records, including design change documentation, in accordance with company procedures.
Support engineering change activities, including documentation updates, and implementation of approved changes.

Qualifications & Experience

Tertiary qualification in Engineering or Science is highly desirable (or similar technical background)
Excellent written communication skills with ability to prepare technical protocols, reports, and documentation.
Strong analytical and problem-solving abilities.
Advanced proficiency in Microsoft Office applications, particularly Word, Excel, and PowerPoint.
Ability to work independently while also collaborating effectively within multidisciplinary teams.
Strong attention to detail and commitment to quality.

Preferred Skills

Knowledge of medical device regulations and quality systems (ISO 13485, ISO 14971, GMP) is advantageous.
Exposure to laboratory testing, materials testing, or validation activities through university projects or industry placements.
Experience analysing data using Excel or statistical tools is desirable.
Familiarity with technical drawings, engineering documentation, and change control processes is highly regarded.

Welcome to impact. Welcome to innovation. Welcome to your new life.

Apply Now

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process engineer jobs

Graduate Validation & Testing Engineer

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