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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

Vice President - Research & Development

  • Clayton
  • $200000 - $250000 per annum

About the company Inoviq is a biotechnology company is 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 Lead, plan and manage the Research and Development (R&D) function of Inoviq to advance the development of technologies and products in accordance with company goals and priorities. This is an executive leadership role reporting to the CEO and responsible for providing R&D leadership, developing best practice research policies, planning R&D strategies, managing R&D projects and motivating the R&D team to achieve departmental and individual objectives. Position requires a results-orientated R&D leader with the strategic vision, product development expertise and commercial experience to lead the development of proprietary technologies, prepare commercially viable R&D plans, manage R&D budget, build a differentiated product portfolio and drive R&D performance to establish this organisation as a leading cancer diagnostic and therapeutic company.  Key deliverables include developing R&D plan and budget, preparing research proposals, protocols, reports, presentations and publications, managing internal and external R&D programs to achieve agreed R&D objectives and reporting on R&D performance. Duties Recruit, lead, manage and mentor a high performing R&D team to achieve agreed departmental and individual objectives. Provide R&D leadership and direction, establish best practice research policies, determine research priorities and drive commercial focus for company research to achieve its vision, mission & objectives. Act as scientific spokesperson for company to internal and external stakeholders including board, scientific community, clinicians, investors, media and public. Prepare and manage R&D Budget in consultation with CEO/CFO to ensure efficient resourcing, capital allocation and expenditure to achieve Company goals. Provide high-level scientific advice and development expertise to CEO on all R&D issues and work collaboratively with executive on business, quality, regulatory and safety initiatives. Skills and Experience Bachelor and Doctoral qualifications in Molecular Biology, Immunology, Cell Biology, Genetics or other relevant field (further business degree also highly regarded). Significant experience in leading, planning, budgeting, managing and reporting on research programs focused on Cell Therapy / Immuno Oncology including biomarker discovery, preclinical research and clinical development of cancer therapeutics and diagnostics to achieve R&D milestones. Proven ability to articulate research vision, develop research strategies and prepare development plans with milestones to achieve technical, development & regulatory objectives. Established R&D track record, credibility and reputation in cancer therapeutics and/or diagnostics including relevant publications, grants and fundraising 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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Life Sciences,Scientific

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.

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Life Sciences,Scientific

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.

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Life Sciences,Scientific

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.

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Life Sciences,Scientific

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.

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