- Salary$40 - $43 per hour
- LocationBroadmeadows
- Job type Contract
- DisciplineScientific
- ReferenceBH-43269
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QCE Scientist Instrumentation (GDIP)
Job description
Benefits
This global biopharmaceutical organisation focuses on developing and delivering life-saving therapies and vaccines. Their Melbourne-based site is a centre of excellence in large-scale plasma manufacturing and advanced biotechnological research.
About the Opportunity
This role plays a critical part in ensuring the integrity and compliance of laboratory instrumentation and systems within the Quality Control Excellence team. You will support the assessment and qualification of laboratory equipment, ensuring adherence to Data Integrity (DI) guidelines and Good Manufacturing Practice (cGMP) standards. Working within a collaborative, safety-driven environment, you will contribute to maintaining high-quality laboratory operations and advancing compliance initiatives across the organisation.
Duties
How to Apply Click apply or contact Georgia Graham – Senior Recruitment Consultant at +61 488 807 453 or ggraham@hpgconnect.com for a confidential discussion.
About Healthcare Professionals Group
Healthcare Professionals Group specialises in healthcare recruitment across clinical research, medical affairs, pharmacovigilance, quality, regulatory affairs, and more.
For more job opportunities, visit www.hpgconnect.com.
- Competitive hourly rate based on experience
- Monday to Friday, standard daytime hours
- Onsite role with access to world-class laboratory facilities
- Join a global biotechnology leader with a strong commitment to quality and innovation
This global biopharmaceutical organisation focuses on developing and delivering life-saving therapies and vaccines. Their Melbourne-based site is a centre of excellence in large-scale plasma manufacturing and advanced biotechnological research.
About the Opportunity
This role plays a critical part in ensuring the integrity and compliance of laboratory instrumentation and systems within the Quality Control Excellence team. You will support the assessment and qualification of laboratory equipment, ensuring adherence to Data Integrity (DI) guidelines and Good Manufacturing Practice (cGMP) standards. Working within a collaborative, safety-driven environment, you will contribute to maintaining high-quality laboratory operations and advancing compliance initiatives across the organisation.
Duties
- Assist with equipment qualification, calibration, and documentation reviews
- Write and execute qualification protocols for laboratory instruments
- Conduct testing to verify system performance (not product testing)
- Support Data Integrity assessments and instrument compliance reviews
- Collaborate with QC and global stakeholders to align with DI standards
- Maintain accurate records in accordance with cGMP and site documentation requirements
- Participate in safety and quality improvement initiatives
- Bachelor’s degree in Biology, Chemistry, Microbiology, or related scientific discipline
- 2–5 years’ experience in a cGMP Quality Control environment
- Hands-on experience with instrument qualification or validation (e.g. HPLC, UV, GC, plate readers)
- Understanding of Data Integrity principles and laboratory process automation
- Knowledge of instrument lifecycle management and documentation systems (LIMS)
- Strong attention to detail, analytical mindset, and problem-solving ability
- Excellent written and verbal communication skills
- Ability to work autonomously and collaboratively within a small team environment
How to Apply Click apply or contact Georgia Graham – Senior Recruitment Consultant at +61 488 807 453 or ggraham@hpgconnect.com for a confidential discussion.
About Healthcare Professionals Group
Healthcare Professionals Group specialises in healthcare recruitment across clinical research, medical affairs, pharmacovigilance, quality, regulatory affairs, and more.
For more job opportunities, visit www.hpgconnect.com.