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.
Senior Validation Specialist
- Parkville
- $0 - $63.41 per hour
Benefits Working within a global team Must have unrestricted work rights/ be able to work unrestricted for 6 months. About the company Work within a large global Biotechnology company that boasts a good company culture that is always expanding. About the role An exciting opportunity for an experienced Senior Validation Specialist to join the Analytical Science & Technology (AS&T) team. This is a pivotal role where you will act as a Subject Matter Expert (SME) in analytical testing methodology, driving method validation, standardization, and robustness across sites. You will also play a key role in troubleshooting technical issues and implementing the latest testing technologies. Key Responsibilities Maintain compliant Quality Control (QC) method validation lifecycle management. Lead troubleshooting investigations for QC test methods and implement solutions through CAPA and Change Control. Oversee method standardization and robustness programs. Develop and enhance analytical test methods, keeping pace with industry advancements. Coordinate and execute intra-site method transfers and provide SME input into regulatory filings and audits. Design and execute experimental projects involving new analytical technologies. Manage and oversee AST project studies, ensuring quality and compliance. Review validation data, identify trends or deviations, and escalate issues to management as necessary. Influence QC leadership on method improvement and replacement strategies. Maintain up-to-date industry knowledge on emerging methods, equipment, and best practices. Requirements Bachelor’s degree in a Science-related field (Chemistry, Biochemistry, or related discipline). Minimum 2 years’ experience in pharmaceutical or biopharmaceutical industries, with increasing responsibilities in Quality Management. Background in method development and experience in a microbiology setting Strong cGMP knowledge and background in Pharmaceutical Quality Control. Hands-on experience with analytical testing techniques and regulatory compliance. Excellent time management and ability to plan and oversee work schedules. Strong communication skills (written & verbal) for documentation, reporting, and collaboration. Knowledge of continuous improvement and root cause analysis methodologies. 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.
Sample Management Technician
- Parkville
- $0 - $47.89 per hour
Benefits Be part of a supportive and stable working environment Working within a global team About the company Work within a large global Biotechnology company that boasts a good company culture that is always expanding. About the opportunity This role is vital in managing clinical and non-clinical samples and materials, ensuring compliance with Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), and Good Research Laboratory Practice (GRLP) standards in a fast-paced research environment. Duties: Manage sample inventory in freezers and refrigerators, performing regular stock checks. Ensure accurate labelling and registration of incoming materials in the Inventory Management system. Coordinate shipments of samples to/from offsite storage facilities. Retrieve and return samples for laboratory testing as requested. Ensure compliance with OECD GLP, ISO/IEC 17025, and CSL policies. Support internal and external audits and contribute to quality assurance processes. Collaborate with scientists, study leads, and quality teams to ensure smooth sample handling. Participate in process improvements and innovation in sample management practices. Requirements: Bachelor’s degree (or equivalent experience) in Life Sciences, Biotechnology, or a related field. 2-3 years experience in sample management, inventory control, or laboratory operations (preferred). Proficiency in electronic laboratory notebooks (ELN), inventory management software, and freezer management systems. Strong attention to detail with the ability to maintain compliance and data integrity. Excellent organizational and communication skills, with a proactive approach to problem-solving. Culture Although a large, global company, they are able to provide a family-like culture and prides itself in improving the lives of others. 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 Graham, Senior Recruitment Consultant on +61370371653 for a confidential discussion.
Microbiology Quality Control Analyst
- Parkville
- $0 - $36.69 per hour
Benefits Be part of a supportive and stable working environment Working within a global team About the company Work within a large global Biotechnology company that boasts a good company culture that is always expanding. About the opportunity In this role, you will perform quality control testing on Products of National Significance (PNS) and Non-Influenza Vaccine (Non-IVV) products, including immunology, biochemistry, and virology assessments. You will also be involved in small animal handling, dosing, and testing, ensuring compliance with Good Laboratory Practice (GLP) and GMP guidelines. Duties: Perform quality control testing on Products of National Significance (PNS) and Non-IVV products, including immunology, biochemistry, and virology. Conduct small animal handling, monitoring, dosing, and testing. Maintain Good Laboratory Practice (GLP) and ensure assay accuracy. Investigate Out of Specification (OOS) test results and recommend process improvements. Maintain GMP-compliant environments, including material and equipment sterilization. Accurately complete and maintain quality records, documentation, and procedures. Must haves Tertiary qualification in Applied Science, Biological Technology, or related disciplines. Hands-on experience in handling and monitoring small animals (knowledge of ethics and regulations is highly regarded). Experience in assay preparation, laboratory testing, and data recording. Proficiency in scientific report writing and computer-based data entry. Flexibility to work across various shifts (day, afternoon, and night). Willingness to undertake required vaccinations for the role. Culture Although a large, global company, they are able to provide a family-like culture and prides itself in improving the lives of others. Why this opportunity is right for you This is a Full-time 9-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.
Quality Control Scientist
- Broadmeadows
- $0 - $43.10 per hour
Benefits Be part of a supportive and stable working environment Working within a global team About the company Work within a large global Biotechnology company that boasts a good company culture that is always expanding. About the opportunity As a QC Analyst – Analytical Technology Scientist, you will play a crucial role in developing, optimizing, and validating chemistry-related analytical methods. You will be responsible for implementing innovative technologies, troubleshooting analytical challenges, and contributing to the continuous improvement of the Quality Control Analytical Technology (QCAT) laboratory. This is a full time 12-month conract position. Resposibilities: Develop, compare, optimize, and validate chemistry-related analytical methods. Design experimental study plans, estimating materials, time, and resources required. Prepare, review, and update standard operating procedures, test protocols, reports, and documentation following cGMP and data integrity requirements. Support project coordination and deliverables under the guidance of the Head of QCAT or delegate. Conduct studies to introduce new analytical techniques and remediate analytical challenges. Investigate deviations, atypical results, and method performance issues. Provide technical assistance, scientific support, and training to colleagues. Maintain compliance with safety, quality, and regulatory requirements. Must have Education: Bachelor’s degree in Chemistry, Biological Sciences, Engineering, or a related technical field. A postgraduate qualification (Master’s or Ph.D.) is preferred. Experience: Minimum of 3 years in a QC or method validation environment, preferably within a cGMP-regulated pharmaceutical/biotech setting. Technical Expertise: Experience with spectroscopy techniques (FTIR, NIR, AAS, UV). Familiarity with direct instrumental measurements (pH, Osmolality, Density, Gravimetry). Proficiency in nitrogen determination by combustion. Knowledge of data integrity policies and software validation (a plus). Health requirement Set B – Informed consent consult, Hepatitis B antibodies only Ishihara colour vision screening Optometry assessment Culture Although a large, global company, they are able to provide a family-like culture and prides itself in improving the lives of others. 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.
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
Senior Recruitment Consultant - Life Sciences
Gemma Staddon
Divisional Manager - Life Sciences