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.
Jobs by Georgia Graham.
Scientific Technician
- Melbourne
- $0 - $51.31 per hour
Benefits Working within a global team Must have unrestricted work rights/ be able to work unrestricted for 1 year min. About the company Work within a large global Biotechnology company that boasts a good company culture that is always expanding. About the role Provide technical support in plasma bioprocessing laboratory settings including bench to kilo scale work, assisting scientists and researchers with experiments, sample preparation, data collection, and equipment maintenance. Duties: Prepare and calibrate lab equipment such as pH meters and density meters. Support experimental execution, including scale-down and scale-up models. Conduct chromatography (FPLC) and ultra-filtration of plasma intermediates at kilo-scale. Assist with ethanol precipitation and buffer preparation. Collect, label, and manage samples for analytical testing. Maintain Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards. Document experiments in Electronic Lab Notebooks (ELNs) as per GxP compliance. Must have: Bachelor's Degree in a Science-related field. 1–2 years of lab experience in a regulated environment. Familiarity with GxP documentation and compliance. Hands-on experience with buffer preparation, pH calibration, and filtration operations. Knowledge of bioprocessing, chromatography, ethanol precipitation, and plasma fractionation is a plus. Excellent teamwork and communication skills. Culture Although a large, global company, they are able to provide a family-like culture and prides itself in improving the lives of others. How to Apply Click apply or contact Georgia Graham – Senior Recruitment Consultant on 03 7037 1653 for a confidential discussion. About Healthcare Professionals Group Healthcare Professionals Group recruits all positions: executive, permanent, contracting/temp, at all levels, across all areas of healthcare - Pharmaceuticals, Biotechnology, Medical Technology and Clinical Care. 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.
Clinical Trials Pharmacy Manager
- Melbourne
- $125000 - $150000 per annum
Benefits Step into a high-impact leadership role in an organisation where your professional development and leadership growth are actively supported Work with a high-performing, highly collaborative pharmacy and research operations team Opportunity to drive innovation and pharmacy process optimisation Exposure to a variety of local and global Phase I–IV studies Strong cross-functional collaboration with clinical, BD, feasibility, and finance teams Direct input into feasibility, trial start-up strategy, and site delivery About the Company This organisation is a leading clinical research site network focused on advancing global health through the expert management of clinical trials. Known for operational excellence, regulatory integrity, and participant-first values, they manage a growing portfolio of studies across a wide range of therapeutic areas. Their pharmacy team plays a critical role in trial execution and protocol compliance. About the Role This is a rare opportunity to lead the pharmacy function at the heart of a thriving clinical trial site. As Clinical Trials Pharmacy Manager, you’ll take ownership of investigational product (IP) operations and step into a pivotal leadership role, guiding a skilled team and ensuring best-in-class processes across a varied study portfolio. You’ll also contribute at a strategic level, working cross-functionally to shape trial start-up, feasibility planning, and pharmacy workflow optimisation. This role is ideal for a pharmacist ready to blend hands-on clinical trial oversight with team leadership and business-aligned decision-making in a fast-growing environment. Duties Manage end-to-end investigational product (IP) operations: receipt, storage, dispensing, accountability, and destruction Ensure full compliance with GCP, pharmacy manuals, protocols, and regulatory standards Lead, support, and develop a multidisciplinary pharmacy team Implement and continuously improve SOPs, workflows, and documentation processes Optimise pharmacy operations to enhance trial efficiency, throughput, and audit-readiness Drive process improvement initiatives, identify system enhancements, and champion best practices Collaborate cross-functionally with clinical, feasibility, finance, and sponsor-facing teams Contribute pharmacy insights to trial feasibility, start-up planning, and operational strategy Participate in audits, CAPA development, and internal quality reviews Skills and Experience Essential: Registered Pharmacist with AHPRA 3+ years clinical trial experience in a pharmacy role 2–3 years general hospital or community pharmacy experience Proficient in Z-Dispense, nCoup, and electronic IP accountability systems Strong understanding of GCP and clinical trial regulatory standards Highly Desirable: Prior team leadership or pharmacy management experience (1–2 years) Hands-on experience with audits and CAPA documentation Company Culture This is a values-driven organisation where collaboration, continuous improvement, and participant care are at the heart of everything. They foster a solutions-focused environment where autonomy is encouraged, and high performance is recognised. How to Apply Click apply or contact Georgia Graham – Senior Recruitment Consultant at +61488807453 or 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.
Clinical Trial Investigator
- Camberwell
- $130000 - $180000 per annum
Benefits Work in a fast-growing clinical research organisation making a global health impact Structured onboarding including 3-week shadowing period with an experienced CTI if required Gain exposure across diverse therapeutic areas in clinical trials Clear pathway for career progression into a Principal Investigator (PI) role Collaborate in a social, supportive, and dynamic team of medical professionals Join a business that values innovation, patient care, and team collaboration About the Company A trailblazing clinical trial organisation committed to improving world health by accelerating medical advancements through high-quality, patient-centered research. With a culture anchored in values, their multidisciplinary team is known for its professionalism, care, and innovation. The company partners with leading sponsors to deliver outstanding trial outcomes through scientific excellence and compassionate care. About the Role As a Clinical Trial Investigator/Sub-Principal Investigator, you will play a hands-on role in the delivery of clinical trial protocols. You'll conduct patient screening, assessments, safety reviews, and support participant compliance, working closely with participants throughout their clinical journey. Your focus on providing quality, empathetic care will help support the current Principal Investigators in managing broader trial responsibilities. This is an ideal opportunity for both junior and experienced doctors passionate about clinical research and patient care. Duties Conduct clinical assessments, screenings, and protocol-related procedures Monitor patient safety and response to therapy Ensure protocol compliance and regulatory documentation per ALCOA+ principles Review participant results and collaborate on medical decision-making Engage with trial sponsors during site visits and audits Participate in training, governance reviews, and continuous improvement discussions Work within a cross-functional clinical operations team Skills and Experience (Happy to consider both experienced and new medical professionals. Prior clinical trials experience is not a neccessity – the company will provide comprehensive training if required) Medical degree with Unrestricted General and/or Specialist Registration AHPRA registration Demonstrated passion for clinical trials or evidence-based medicine Strong interpersonal skills and a compassionate, patient-focused approach Critical thinking and initiative in problem-solving Ability to adapt, work flexibly, and contribute ideas in a growing team Willingness to work collaboratively in a social, energetic team of CTIs and PIs Company Culture You’ll be joining a collaborative and future-focused team in a dynamic, social, and values-driven enironment where team members are motivated by the real-world impact of clinical trials. How to Apply Click apply or contact Georgia Graham – Senior Recruitment Consultant at +61488807453 or 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.
Quality Control Analytical Technology Scientist
- Broadmeadows
- $40 - $43 per hour
Benefits Work with one of the world’s most respected biopharma organisations Join a high-calibre scientific team working on impactful therapeutic products Gain exposure to innovative immunoassay and biochemistry techniques Standard Monday to Friday hours Collaborative team of specialists and career-enhancing experience in GMP About the company Work within a large global Biotechnology company that boasts a good company culture that is always expanding. About the opportunity This 12-month contract role sits within the Quality Control Analytical Technologies team, supporting analytical activities related to method development, validation, and transfer. Based in a biochemistry-focused lab environment, you’ll play a critical role in the scientific and regulatory support of biological product testing, reporting to the Head of QCAT. This is a fantastic opportunity for a QC Scientist or Analyst with biochemistry or molecular biology experience to take on a project-based scientific role within a supportive and quality-driven team. Resposibilities: Develop, validate, and transfer analytical methods for biological products Design and execute experimental plans in accordance with project objectives Prepare and review scientific documentation including SOPs, protocols, and validation reports Perform analytical testing using immunoassay-based techniques (e.g., ELISA, nephelometry) Ensure accuracy and data integrity in accordance with GMP and regulatory standards Participate in project meetings and regulatory discussions Coordinate timelines and schedules for yourself and supporting analysts Provide insights and support for process improvements, investigations, and quality submissions Must have Bachelor’s degree (or higher) in Biochemistry, Molecular Biology, Chemistry, or related scientific field Minimum 2–3 years’ experience in a regulated laboratory environment (GMP or similar) Hands-on experience in analytical method development or validation for biologics Familiarity with immunoassays (ELISA, nephelometry) and data analysis tools Strong technical writing skills (SOPs, validation protocols, test reports) Ability to work both independently and collaboratively in a project-driven setting Proven organisational and time management skills Must have full working rights in Australia Health requirement Audiometry Set B – Informed consent consult, Hepatitis B antibodies only Set A – Informed consent consult, HIV, Hepatitis C & Hepatitis B antibodies and Antigen Culture You’ll be joining a tight-knit team of six within a large, mission-driven organisation where scientific excellence, integrity, and collaboration are core values. The team encourages autonomy, proactive problem-solving, and mutual support, with access to world-class systems and technology. Why this opportunity is right for you This is a Full-time 12-month contract opportunity based in Melbourne working onsite Monday to Friday. How to Apply Click apply or contact Georgia, Senior Recruitment Consultant on +61370371653 for a confidential discussion.
Sterility Assurance Specialist
- Broadmeadows
- $55 - $56.44 per hour
Benefits Working within a global team Must have unrestricted work rights/ be able to work unrestricted for 7 months About the company Work within a large global Biotechnology company that boasts a good company culture that is always expanding. About the role As a Sterility Assurance Specialist, you will report to the Sterility Assurance Monitoring Team Lead and play a critical role in maintaining and enhancing sterility assurance controls. Your expertise will ensure the highest standards in environmental and personnel monitoring, in-process testing, finished product testing, and microbiological method development. Key Responsibilities: Oversee the lifecycle management of sterility assurance monitoring controls. Conduct Environmental and Personnel monitoring, in-process testing, and finished product testing. Participate in the validation and qualification of the facility, utilities, equipment, processes, personnel, and methods. Lead initiatives in cleaning, disinfection, hygiene, operator training, gowning, and facility design. Collaborate with global function leads and site leadership to ensure continuous adherence to regulatory and company standards. Drive continuous improvement in sterility assurance governance. Manage trending and data analysis for sterility monitoring. Act as the point of contact for a bulk facility, managing stakeholder relationships and driving project goals. Must have: Bachelor of Science (Microbiology preferred) or relevant scientific degree. Experience in Aseptic manufacturing, ideally within the pharmaceutical industry. Expertise in Environmental Monitoring, Sterility Assurance, GMP, and GDP. Ideally seeking someone who has worked in Pharma industry Proficient in data management and trending analysis. Excellent stakeholder management and communication skills. Ability to work autonomously and drive sterility assurance projects to completion. Culture Although a large, global company, they are able to provide a family-like culture and prides itself in improving the lives of others. How to Apply Click apply or contact Georgia Graham – Senior Recruitment Consultant on 03 7037 1653 for a confidential discussion. About Healthcare Professionals Group Healthcare Professionals Group recruits all positions: executive, permanent, contracting/temp, at all levels, across all areas of healthcare - Pharmaceuticals, Biotechnology, Medical Technology and Clinical Care. 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.
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.
Jo Turner
Divisional Manager - Business Support, Operations and Life Sciences
Davina Ocansey-Gibson
Specialist Manager - Life Sciences
Gemma Staddon
Divisional Manager - Life Sciences