In-Demand Process engineer Jobs

Graduate Validation & Testing Engineer
LivaNova —Melbourne VIC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Lead Process Engineer - Capital Projects
Thales —Bendigo VIC
- Full-time
- Management
- Engineering
- Manufacturing
- Health insurance
- Parental leave
Senior Process Engineer – Water Treatment
Stantec —Sydney NSW
- Part-time
- Writing skills
- Communication skills
- Negotiation
- Work from home
- Employee assistance program
Process Engineer
PharmaCare Group —Prestons NSW
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
- Parental leave
Quick Apply
2d
AI ML Engineer
Infosys Singapore & Australia —Melbourne VIC
- Full-time
- Azure
- Management
- Computer Science
Quick Apply
Process Engineer
Senior Leadership InfraBuild —Laverton VIC
- Engineering
- Analysis skills
- Manufacturing
- Health insurance
- Parental leave
Principal Process Engineer - Resources Consulting
Worley —Brisbane QLD
- Full-time
- Engineering
- Microsoft Office
- Bachelor's degree
9d
Data Engineer
Infosys Singapore & Australia —Melbourne VIC
- Full-time
- Hybrid work
- SQL
- AWS
Quick Apply
11d
Senior Process Engineer
Peabody Energy —Glenden QLD
- Monday to Friday
- Analysis skills
- Communication skills
- Relocation assistance
- Employee assistance program
Senior / Principal Process Engineer (Wastewater)
Stantec —Melbourne VIC
- Part-time
- Employee assistance program
Senior Process Safety & Risk Engineer
Ampol —Lytton QLD
- Full-time
- Management
- Engineering
- Leadership
- Parental leave
- Fuel discount
Senior Process Engineer
Ausenco —Perth WA
- Full-time
- Engineering
- Analysis skills
- Work from home
- Parental leave
Advance Software Engineer
Infosys Singapore & Australia —Melbourne VIC
- Full-time
- Hybrid work
- Azure
- Computer Science
- DevOps
Quick Apply
GHD Graduate Program 2026/27 - WA - Process Engineers
GHD —Perth WA
- Full-time
- Communication skills
3d
Senior Engineer - Process Engineering
Water Corporation —Leederville WA
- From $135,693 a year
- Remote
- Engineering
- Annual leave
- Work from home
1d
Engineer - Process Control & Instrumentation
Orica —Mayfield NSW
- Full-time
WCM (Process Engineer)
CSR —Cecil Park NSW
- Full-time
- Analysis skills
- Manufacturing
- Communication skills
- Parental leave
- Employee assistance program
Quick Apply
11d
Senior Process Engineer - Midstream
PLS —Pilbara WA
- Administrative experience
- Analysis skills
- Communication skills
- Employee assistance program
13d
Process Control Network Engineer (PCN)
Accenture —Perth WA
- Full-time
- Computer Science
- Engineering
- Bachelor's degree
Regional Process Engineer
Cleanaway —Silverwater NSW
- Full-time

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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

Refine Your Search

process engineer jobs

Graduate Validation & Testing Engineer

Lead Process Engineer - Capital Projects

Senior Process Engineer – Water Treatment

Process Engineer

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WCM (Process Engineer)

Senior Process Engineer - Midstream

Process Control Network Engineer (PCN)

Regional Process Engineer

I want to receive the latest job alert for process engineer

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

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