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Scientific

Skilled scientists drive the innovations that lead to groundbreaking advancements in healthcare, ultimately improving patient outcomes and the quality of life for countless individuals.

Welcome to the HPG page dedicated to Scientific and Research recruitment. At HPG, we specialise in connecting exceptional talent with rewarding healthcare roles, including critical positions in scientific research and development.

Our expert recruitment team focuses on sourcing top-tier candidates for roles in the scientific industry, ensuring our clients benefit from professionals who lead cutting-edge research and contribute to the development of life-saving treatments. From preclinical development scientists who shape the future of healthcare innovations to regulatory and compliance experts ensuring the highest standards in medical products, we cover the full spectrum of scientific roles.

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Are you looking for a fulfilling career in the scientific sector? HPG is here to help you find the perfect opportunity. We offer a wide range of roles, from entry-level scientific positions to senior-level roles requiring specialised knowledge and extensive experience. Whether you're interested in research, quality and compliance, or regulatory affairs, we have the expertise to match your skills with employers who are at the forefront of healthcare advancements.ns.

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Jobs in Scientific.

Scientific,Life Sciences

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.

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Scientific,Life Sciences

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.

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Scientific

Senior Scientist - Diagnostics

  • Clayton
  • $110000 - $120000 per annum, Benefits: Attractive salary on offer

About the company Inoviq is a biotechnology company who are developing next-generation diagnostics and therapeutics for cancer. Their diagnostics portfolio utilises proprietary exosome and glycomic technologies to develop blood tests for earlier detection, treatment selection and monitoring of cancer to improve patient outcomes.     About the opportunity This is a newly created role for a highly motivated diagnostics scientist to join a collaborative and commercially focused R&D team.  In this role you will lead diagnostic programs to translate cutting-edge technologies into clinically and commercially relevant products.  The successful candidate will play a pivotal role in advancing novel diagnostic tests from biomarker translation through validation to registration.   Duties Provide leadership of diagnostics programs to develop clinically and commercially viable products that have a meaningful impact for patients, clinicians, and healthcare. Plan, manage, execute, and report on biomarker discovery, analytical and clinical validation studies for in vitro diagnostics to meet agreed technical, development and registration milestones on time and within budget. Ensure the maintenance of accurate laboratory records to secure intellectual property and document design control in accordance with regulatory guidelines. Manage external projects with diagnostics collaborators, partners, contract research/manufacturing organisations and consultants to meet agreed timelines, budgets, and outcomes. Perform and report data analyses of biomarker and assay performance using relevant statistical packages. Identify and evaluate new diagnostic technologies and product opportunities. Supervise, train and manage the diagnostics team. Liaise with regulatory consultants and agencies to ensure alignment with global LDT and IVD requirements.     Skills and Experience PhD in Molecular and Cell Biology, Biochemistry, Genetics, Endocrinology, Immunology, or another relevant field. Minimum 5+ years of relevant laboratory research experience including 3+ years as a senior scientist working in a pharmaceutical or diagnostics industry setting with responsibility for diagnostics development. Proven track record in clinical diagnostics development including biomarker discovery, analytical validation, clinical validation of in vitro diagnostics for Oncology, or other relevant area. Significant research management experience with responsibility for design and execution of research plans, statistical data analysis and interpretation, progress reporting, and preparation of technical reports, publications and presentations on research findings. Knowledge of immuno- and molecular diagnostic development, standard diagnostic instrument platforms and IVD medical device regulatory requirements. Strong planning, critical thinking, and analytical skills with ability to solve specific research questions and technical issues. Broad knowledge of omics techniques Strong interpersonal, communication and presentation skills with ability to communicate both orally and in writing.   How to Apply Click apply or contact Jo Turner, Senior Specialist Consultant on 03 9938 7120 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.com

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Scientific

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.

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Scientific

Medical Science Liaison - Cardiometabolic (12-month Contract)

  • Melbourne
  • Competitive

Benefits Territory Expansion: Opportunity to lead and grow multiple Cardiometabolic territories at a national level. Attractive Compensation: Generous salary package inclusive of performance-based bonus and vehicle allowance. Robust Strategic Backbone: Strong national Medical Science Liaison framework, with direct guidance from multiple Medical Advisors. About the Company This global biopharmaceutical leader is celebrated for its unwavering focus on innovation and top-tier performance across several therapeutic domains. Through a commitment to continuous enhancement, they have redefined patient outcomes, pioneered drug development progress, and transformed lives worldwide. With an ever-expanding pipeline, they remain poised to lead the field in specialized healthcare solutions. About the Opportunity In this Medical Science Liaison role, you will be instrumental in shaping strategic direction and decisions throughout the drug development journey. Leveraging your deep clinical knowledge and commercial awareness, you will translate field insights into actionable strategies, influencing key milestones in therapeutic advancement. Your work will help redefine standards of care in critical disease areas. Responsibilities KOL Engagement: Build and nurture professional relationships with KOLs in hospitals, pharmaceutical environments, and academic settings. Thought Leadership: Demonstrate authoritative expertise in every professional engagement. Strategic Input: Drive and influence comprehensive strategies supporting therapeutic innovation and portfolio growth. Obstacle Navigation: Anticipate and address barriers, utilizing networks to strengthen product positioning and adoption. Skills and Experience Required MSL or Cardiometabolic Background: Proven experience in an MSL role or an advanced academic foundation in Cardiometabolic science. Clinical-Commercial Insight: Deep grasp of the intersection between clinical excellence and commercial viability. Persuasive Communication: Skilled in delivering clear, impactful messaging to KOLs and stakeholders across multiple levels. Culture Their dynamic culture focuses on career development, collaboration, innovation, passion, and patient care. How to Apply To express your interest, please contact Rohan at rlallbeeharry@hpgconnect.com. About Healthcare Professionals Group  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.

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