Job Title

BenefitsWork with one of the worlds most respected biopharma organisationsJoin a high-calibre scientific team working on impactful therapeutic productsGain exposure to innovative immunoassay and biochemistry techniquesStandard Monday to Friday hoursCollaborative team of specialists and career-enhancing experience in GMPAbout the companyWork within a large global Biotechnology company that boasts a good company culture that is always expanding.About the opportunityThis 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, youll 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 productsDesign and execute experimental plans in accordance with project objectivesPrepare and review scientific documentation including SOPs, protocols, and validation reportsPerform analytical testing using immunoassay-based techniques (e.g., ELISA, nephelometry)Ensure accuracy and data integrity in accordance with GMP and regulatory standardsParticipate in project meetings and regulatory discussionsCoordinate timelines and schedules for yourself and supporting analystsProvide insights and support for process improvements, investigations, and quality submissionsMust haveBachelors degree (or higher) in Biochemistry, Molecular Biology, Chemistry, or related scientific fieldMinimum 23 years experience in a regulated laboratory environment (GMP or similar)Hands-on experience in analytical method development or validation for biologicsFamiliarity with immunoassays (ELISA, nephelometry) and data analysis toolsStrong technical writing skills (SOPs, validation protocols, test reports)Ability to work both independently and collaboratively in a project-driven settingProven organisational and time management skillsMust have full working rights in AustraliaHealth requirementAudiometrySet B Informed consent consult, Hepatitis B antibodies onlySet A Informed consent consult, HIV, Hepatitis C & Hepatitis B antibodies and AntigenCultureYoull 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 youThis is a Full-time 12-month contract opportunity based in Melbourne working onsite Monday to Friday.How to ApplyClick apply or contact Georgia, SeniorRecruitment Consultant on+61370371653for a confidential discussion. #J-18808-Ljbffr