Georgia Graham

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Georgia Graham

Senior Recruitment Consultant

I focus on Quality and Scientific.

The roles I work on include:

Quality Assurance & Quality Control (QA/QC)
Regulatory Affairs
Research & Development
Medical Laboratory Science
Clinical & Scientific Affairs
Validation & Compliance
Microbiology & Biotech Manufacturing

After completing my Master’s degree, I wanted to find a career that would leverage my scientific background in a people-centric way. I gained two years of valuable experience at a scientific recruitment agency in the UK and was excited to continue on this path with HPG after relocating to Australia.

I hold a Bachelor’s degree in Biomedical Science and a Master’s in Prenatal Genetics and Fetal Medicine. My scientific expertise allows me to deeply understand the technical and regulatory landscape of the life sciences industry.

With this strong foundation and a commitment to delivering exceptional recruitment outcomes, I am passionate about connecting professionals with the right opportunities to drive innovation and excellence in healthcare, pharmaceuticals, and life sciences.

Specialising in

Jobs by Georgia Graham.

Scientific

QCE Scientist Instrumentation (GDIP)

Broadmeadows
$40 - $43 per hour

Benefits 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 About the Company 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 Skills and Experience 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 Culture The team operates in a supportive and collaborative environment that encourages continuous learning and professional growth. You’ll join a motivated group of professionals dedicated to maintaining high-quality standards and contributing to innovative global healthcare solutions. 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.

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Scientific

QC Scientist - 40120

Broadmeadows
$41 - $43 per hour

Benefits Competitive salary package Work with a globally recognised biotechnology leader known for scientific excellence and patient impact About the Company This global biopharmaceutical organisation is dedicated to developing and delivering innovative therapies that improve the quality of life for people with rare and serious diseases. About the Opportunity The QC Analytical Technology Scientist plays a pivotal role within the Quality Control Analytical Technology (QCAT) team, driving analytical innovation and method lifecycle management. This position is responsible for planning and delivering projects and investigations, supporting analytical method development, validation, and transfer. Working collaboratively within a high-performing technical team, this role supports the integration of new technologies and ensures compliance with cGMP standards to maintain product quality and regulatory alignment. Duties Develop, plan, and execute analytical studies and investigations aligned with QCAT objectives Prepare and review SOPs, test procedures, protocols, and study documentation Conduct method development, qualification, validation, and transfer between QC, R&D, and external partners Ensure adherence to cGMP, data integrity, and quality documentation standards Participate in audits, inspections, and regulatory submissions as required Support maintenance and calibration of QC laboratory instrumentation Provide technical assistance, training, and mentorship to colleagues Actively contribute to safety investigations, improvements, and innovation initiatives Skills and Experience Bachelor’s degree in Engineering, Physical, or Biological Sciences (postgraduate qualification desirable) Minimum 3 years’ experience in cGMP Quality Control or at least 1 year in analytical method development for biological products Proven experience in analytical method development, validation, or transfer Understanding of analytical method lifecycle management and cGMP principles Strong problem-solving and data interpretation skills Excellent communication, documentation, and teamwork capabilities Experience with LIMS and quality management systems advantageous Culture You’ll join a collaborative, safety-focused environment where scientific curiosity and continuous improvement are encouraged. The team values integrity, innovation, and high performance, fostering an inclusive and supportive culture that promotes personal and professional development. How to Apply Click apply or contact Georgia Graham – Senior Recruitment Consultant at ggraham@hpgconnect.com for a confidential discussion. About Healthcare Professionals Group Healthcare Professionals Group specializes in healthcare recruitment across all areas, including clinical research, medical affairs, pharmacovigilance, and more. Medical Affairs & Life Sciences Recruitment – Clinical Research, Market Access, Medical Affairs, Pharmacovigilance, Quality, Data Management, Regulatory Affairs, Scientific Commercial Recruitment – Marketing, Sales, Analytics, Government and External Affairs Business Operations & Infrastructure Recruitment – Administration, Customer Service, Engineering, Finance, Human Resources, IT, L&D, Legal, Manufacturing, Operations, Supply Chain, Warehouse Clinical Care Recruitment – Allied Health, Aged Care, General Practice, Medical Imaging, Medical Management, Medical Specialties, Nursing For more job opportunities, visit www.hpgconnect.com.

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Clinical Research

Clinical Trial Nurse Manager

Melbourne
$120000 - $135000 per annum

Benefits Competitive salary package Full-time, permanent position based in Melbourne Work within a leading clinical research centre contributing to global health improvements About the Company This organisation is a respected clinical research centre dedicated to improving world health and accelerating medical advancements by expertly managing clinical trials. About the Opportunity As the Clinical Trials Nurse Manager, you will lead and manage the nursing team to ensure outstanding patient safety, care, and operational excellence. You will be responsible for overseeing clinical trial nursing operations, compliance, and documentation standards, while supporting trial start-up and efficiency. This role is pivotal in ensuring the successful delivery of world-class clinical trials and the advancement of medical knowledge. Duties Provide leadership and oversight to the nursing team, managing daily operations Ensure patient safety and accurate administration of investigational products Oversee trial start-up, ensuring nursing protocols and resources are in place Manage recruitment, training, and delegation of nursing staff across protocols Maintain compliance with GCP, ALCOA-C, protocols, and regulatory standards Foster continuous improvement, safety, and compliance culture within the team Collaborate with sponsors, CROs, investigators, and internal stakeholders Support documentation standards, audits, and process improvements Skills and Experience Current registration with AHPRA (mandatory) Tertiary qualifications in Nursing 3+ years’ experience as a Clinical Trials Research Nurse 3+ years’ experience in leadership/management (ANUM or NUM roles) Knowledge of Phases 1–4 of clinical trials Experience with GCP, compliance, and clinical documentation standards Strong customer-centric focus, ensuring positive patient and stakeholder experience Proven ability to engage and liaise effectively with sponsors, CROs, and investigators Excellent leadership, communication, and problem-solving skills Culture You will join a collaborative and values-driven workplace that promotes safety, continuous improvement, and professional growth. The organisation encourages adaptability, innovation, and accountability while fostering a supportive and engaging 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.

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Engineering

Field Service Engineer

Perth
$95000 - $105000 per annum

Benefits Competitive base salary package Additional on-call compensation for after-hours site visits Clear career progression pathway, with structured training including international exposure Work with a globally recognised leader in medical technology About the Company This organisation is a global leader in medical technology, dedicated to advancing health through innovative products and solutions. With a strong presence in healthcare, they are committed to developing transformative technologies that support patients and providers worldwide. About the Opportunity As a Field Service Engineer, you will be responsible for supporting market-leading automated robotic medication dispensing equipment across Western Australia. You will provide both hardware and software servicing, preventative maintenance, diagnostics, and customer training. This role is pivotal in ensuring the reliability and safety of critical medical devices, directly supporting the healthcare system. With dedicated training and a clear progression path, this is an opportunity to build a long-term career within medical electronics. Duties Provide remote and on-site support for electro-medical equipment, including diagnostics, repairs, and upgrades Conduct preventative maintenance, electrical safety testing, and performance checks Monitor and resolve service desk cases, escalating where required Maintain accurate records of service activities in compliance with standards Provide technical sales support and assist in workflow/system reviews Participate in structured training programs locally and internationally Ensure compliance with Australian Standards and company safety policies Occasional interstate and regional travel as required Skills and Experience Tertiary qualification (Degree or TAFE Level 3/4) in Electrical, Electronics, or Electromechanical field Minimum 2+ years’ experience in servicing electrical/electromechanical equipment – ideally in medical devices, automation, or robotics Strong server knowledge and remote diagnostics experience Restricted electrical license highly desirable Ability to work independently while managing your own WA territory Excellent communication and customer service skills Flexibility to support after-hours and on-call work as rostered Culture You will be joining a small but growing WA team, reporting directly to the WA Team Lead. The business values autonomy, proactive problem-solving, and technical excellence. The organisation invests heavily in professional development, providing structured training and a long-term career pathway, while fostering a supportive, collaborative work 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.

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Engineering

Service Repair Technician

Noble Park
$80000 - $90000 per annum

Benefits Base salary of $80,000 – $90,000 + super Ongoing training on dental and medical-grade equipment Immediate start available for the right candidate Hybrid mix of in-house and on-site work Work with a global leader in dental technology offering long-term career stability About the Company This organisation is a global provider of dental equipment and consumables, supporting clinics and laboratories across Australia. Privately owned, they pride themselves on integrity, longevity, and customer service excellence. About the Opportunity As Service Repair Technician, you will play a key role in supporting customers by repairing, maintaining, and testing critical dental equipment. Based at the Noble Park facility, you’ll also provide occasional on-site installations and servicing. This role is vital in ensuring equipment reliability, safety, and compliance, helping dental professionals deliver high-quality care. With training provided, this is a chance to develop expertise across a broad range of electromechanical systems in a supportive, collaborative team. Duties Perform in-house repairs on dental equipment (e.g., curing lights, milling machines, diagnostic devices) Conduct mechanical and electrical diagnostics using manuals, systems, and test equipment Support on-site repairs and installations (local travel, occasional interstate travel) Install and configure new equipment, including calibration and functional testing Ensure compliance with quality systems, safety procedures, and documentation standards Log service work and update history in systems such as SAP and Salesforce Collaborate with customer service, contractors, and the broader repair team Participate in ongoing training for new equipment, updates, and compliance changes Skills and Experience Minimum 3 years’ hands-on experience in dental equipment repair OR related fields such as medical devices Strong technical expertise across electromechanical systems Proven experience in regulated environments with QA, compliance, or safety controls Technical trade qualification in electronics, electrical, mechatronics, or similar discipline Desirable: Electrical Disconnect/Reconnect Licence & X-ray equipment licence Familiarity with SOPs, technical documentation, and accurate record keeping Experience working autonomously or in field-based service roles Strong problem-solving, task prioritisation, and communication skills Culture This is a values-driven, privately owned business with a strong focus on integrity, accountability, and teamwork. The Customer Care division has long-tenured members who work collaboratively, take ownership of their responsibilities, and pride themselves on delivering quality service. Candidates are carefully matched to ensure alignment with the company’s culture of mutual respect and support. 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. Healthcare Professionals Group specializes in healthcare recruitment across areas such as medical devices, life sciences, clinical research, and operations. For more job opportunities, visit www.hpgconnect.com. for a confidential discussion.

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Scientific

QC Microbiologist

Broadmeadows
$35 - $38 per hour

Benefits Competitive hourly contractor rate + super Work with a global biopharmaceutical manufacturer operating modern GMP‑compliant QC laboratories and systems. About the Company A global biopharmaceutical manufacturer supplying critical biologics to patients worldwide, with mature quality systems and a strong culture of compliance and safety. About the Opportunity Join a high‑performing QC Microbiology team to support an upcoming project, ensuring product quality through routine microbiological testing in a regulated GMP environment. Day‑to‑day you’ll focus on environmental monitoring, biological indicator testing and microbial enumeration, as well as accurate data capture and reconciliation in LIMS. Duties Perform environmental monitoring (viable and non‑viable) in classified areas. Conduct biological indicator testing and microbial result reading/enumeration. Complete data entry and sample reconciliation; maintain accurate records in LIMS. Prepare media; perform growth promotion/kit qualification; manage reagents and consumables. Ensure equipment/facilities are maintained and calibrated; perform basic troubleshooting. Follow GDP/GMP, SOPs and test methods; assist with OOS/invalid result investigations and documentation. General laboratory housekeeping and stock control; support 5S and continuous improvement activities. Skills and Experience Degree in Microbiology, Biotechnology or Pharmaceutical Sciences (or related). Experience in a pharmaceutical QC microbiology laboratory with solid GMP/GLP knowledge. Hands‑on with environmental monitoring, BI testing, plate reading/enumeration and media prep. Competent with LIMS and Windows‑based applications; strong documentation (GDP) skills. Able to follow complex SOPs, manage time effectively and work with minimal supervision. Culture Safety‑first, compliance‑driven and collaborative. You’ll join a supportive team that values training, open communication, and continuous improvement within a structured GMP framework. How to Apply Click apply or contact Georgia Graham – Senior Recruitment Consultant at ggraham@hpgconnect.com for a confidential discussion. About Healthcare Professionals Group Healthcare Professionals Group specializes in healthcare recruitment across all areas, including clinical research, medical affairs, pharmacovigilance, and more. Medical Affairs & Life Sciences Recruitment – Clinical Research, Market Access, Medical Affairs, Pharmacovigilance, Quality, Data Management, Regulatory Affairs, Scientific Commercial Recruitment – Marketing, Sales, Analytics, Government and External Affairs Business Operations & Infrastructure Recruitment – Administration, Customer Service, Engineering, Finance, Human Resources, IT, L&D, Legal, Manufacturing, Operations, Supply Chain, Warehouse Clinical Care Recruitment – Allied Health, Aged Care, General Practice, Medical Imaging, Medical Management, Medical Specialties, Nursing For more job opportunities, visit www.hpgconnect.com.

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Clinical Research

Clinical Research Manager

Melbourne
$118000 - $135000 per annum

Benefits Salary packaging available Sign-on bonus considered Be part of an organisation committed to health equity and impact About the Company This is a pivotal role leading the planning, execution and management of a clinical study for an innovative diagnostic device as it progresses toward regulatory submission. You will oversee trial protocols, ethics and governance submissions, quality systems, and regulatory compliance to ensure trials are delivered to the highest standard. The role will also involve supporting project management across other diagnostic initiatives, contributing to best practice implementation, and advancing medical knowledge. Duties Develop, review and finalise study protocols for ethics submission Draft and manage investigational brochures for ethics and regulatory approval Create, submit and manage ethics and governance applications and amendments Manage trial documentation, case report forms, reports and essential files Identify, assess and oversee trial sites, including site visits and investigator engagement Oversee participant recruitment and ensure study milestones are met Manage study operations including clinical supply logistics, safety monitoring, adverse event reporting and audits Apply ISO9001 principles and contribute to SOP development and quality documentation Collaborate with research staff, investigators, industry partners and regulatory authorities Lead cross-functional teams, manage timelines, budgets and project deliverables Provide verbal and written reports to management and stakeholders Support data management practices, tools and software to ensure compliance Travel to trial sites and relevant seminars/meetings as required Skills and Experience Bachelor of Science/Biomedical Science or related discipline (essential) Minimum 3 years’ senior level experience in medical device or diagnostics clinical trials (IVD highly desirable) Strong knowledge of clinical governance, ethics submissions, and site coordination Proven ability in protocol writing, regulatory pathways, and investigational product planning Familiarity with ISO9001 quality systems and SOP development Experience with in-vitro diagnostic assay studies highly regarded Strong project management skills, with experience using project management tools (e.g., MS Project) Good communication skills and stakeholder management, with a collaborative and customer-focused approach Motivated, curious, and eager to develop within the diagnostics/IVD space Culture The organisation is purpose-driven, with a strong alignment to health equity and improving outcomes for vulnerable communities. Staff engagement is high, with a culture that values inclusiveness, respect, and collaboration. It is a supportive and motivated workplace that encourages professional growth and impact. 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.

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COMBINED EXPERIENCE

At HPG, we pride ourselves on bringing together a diverse group of professionals with extensive backgrounds in the healthcare recruitment industry. Our combined years of experience and specialised knowledge ensure that we deliver unparalleled service to our clients and candidates. By working collaboratively, we harness our collective expertise to meet and exceed your goals and expectations, providing tailored solutions and exceptional support every step of the way. Discover how our unified team effort drives success in every project we undertake.