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.
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.
Analyst - QC Sample Management
- Broadmeadows
- $36 - $38 per hour
Benefits Work with one of the world’s most respected biopharma organisations Suitable for graduate and early career scientists Join a high-calibre scientific team working on impactful therapeutic products Gain exposure to innovative QC sample management techniques 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. With state-of-the-art laboratories, you’ll join a passionate team dedicated to maintaining the highest standards of quality, safety, and regulatory compliance. About the role: This role sits within the Quality Control function of a global biopharmaceutical manufacturer and is responsible for supporting cleanroom operations through environmental and utility sampling. The position involves gowning into graded cleanroom environments and following strict protocols to support product quality and regulatory compliance. Responsibilities: Perform viable and non-viable environmental monitoring (air, surfaces, cleanroom areas) Collect and manage samples of water, pure steam, and compressed gases Accurately log and submit samples using LIMS systems Gown and work within graded cleanroom environments (Grades A–D) Follow GMP protocols and site SOPs for all sampling and handling activities Support investigations into deviations or environmental monitoring issues Communicate any sampling delays or issues that may impact timelines Collaborate with team members to ensure consistent sampling coverage across site Requirements: Best suited for recent graduates and early career scientists Bachelor of Science e.g. Microbiology (MSc and above are overqualified) Must have relevant working rights for 12 month contract role Comfortable working in GMP-regulated environments Clear written and verbal communication skills Ability to follow structured procedures and work as part of a team-based QC function Willingness to work in a physically active role, moving between manufacturing areas Culture: The team culture is structured, supportive, and compliance-focused, with a strong emphasis on teamwork, clear communication, and following procedures. It’s a hands-on role in a regulated environment where reliability, consistency, and accountability are highly valued. Why this opportunity is right for you This is a Full-time 12-month contract opportunity based in Melbourne How to Apply Click apply or contact Georgia, Senior Recruitment Consultant on ggraham@hpgconnect.com for a confidential discussion. Health requirement Flu Vaccination required Audiometry Ishihara colour vision screening
Analyst QC Chemistry
- Parkville
- $35 - $37 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 QC Chemistry 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. With state-of-the-art laboratories, you’ll join a passionate team dedicated to maintaining the highest standards of quality, safety, and regulatory compliance. About the Opportunity We’re seeking a dedicated Quality Control Chemist to perform crucial analytical testing activities, ensuring the ongoing safety and quality of the organisations life-saving products. This role provides you with the opportunity to utilize your technical expertise within a high-performing team and significantly contribute to public health. Responsibilities: Conduct routine laboratory testing of products including raw materials and finished goods. Perform wet chemistry techniques, titration, pH, conductivity testing, HPLC, GC-MS, and other analytical methods. Ensure precise sampling, analysis, and accurate logging into Laboratory Information Management Systems (LIMS). Adhere strictly to Good Manufacturing Practice (GMP) and internal data integrity standards. Conduct equipment calibration, validation, and preventive maintenance activities. Participate in out-of-specification investigations and support resolution activities. Assist with laboratory documentation, protocols, and SOP updates to maintain regulatory compliance. Requirements: Tertiary qualification in Chemistry, Biochemistry, Pharmaceutical Science, or related discipline. Demonstrated laboratory experience, ideally in pharmaceuticals or biotech sectors. Proven proficiency in analytical methods such as HPLC, GC-MS, titration, wet chemistry, and physical testing techniques. Familiarity with LIMS and other electronic quality management platforms. Sound knowledge and experience with GMP, GLP, and regulatory compliance standards. Excellent attention to detail, analytical thinking, and problem-solving abilities. Strong written and verbal communication skills. Ability to work effectively in a team and independently manage tasks to deadlines. Culture You’ll be joining a friendly team of 8-14 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 5-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.
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
Eve Cooke
Senior Recruitment Consultant - Life Sciences
Davina Ocansey-Gibson
Specialist Manager - Life Sciences
Gemma Staddon
Divisional Manager - Life Sciences