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An exciting opportunity has become available for an experienced Senior Quality & Regulatory Affairs Specialist to join an innovative Australian medical device company with products approved across Australia, Europe, Japan and the USA. This is a rare opportunity to step into a broad QA/RA position within a collaborative and highly technical environment, where you'll work closely with leadership, engineering and product development teams while helping drive the next phase of growth. If you enjoy being hands-on, solving problems, improving systems and seeing the direct impact of your work, this could be the ideal next step in your career. About the Role Reporting to the Head of Quality & Regulatory Affairs, you'll play an integral role in maintaining quality and regulatory compliance across multiple international markets while supporting upcoming audit activities and future product development initiatives. This is a broad, hands-on role offering exposure across Quality Assurance, Regulatory Affairs, engineering, manufacturing and product development within a collaborative and highly technical environment. Key ResponsibilitiesSupport Regulatory Affairs activities across Australia, Europe, Japan and the United States, ensuring ongoing compliance with applicable regulatory requirements.Prepare, review and maintain regulatory submissions, technical files and supporting documentation.Manage compliance activities in accordance with EU MDR, MDSAP, TGA, FDA and PMDA requirements.Support regulatory compliance for both hardware and software-based medical devices.Work closely with Engineering, R&D and Product Development teams to assess regulatory requirements associated with product changes and future technologies.Review, update and maintain Quality Management System (QMS) documentation, procedures and work instructions.Identify compliance gaps and drive corrective and preventive actions to support continuous improvement.Support supplier audits, external audits and surveillance audit activities.Contribute to CAPA, risk management, post-market surveillance and ongoing quality assurance initiatives.Liaise with internal stakeholders, external auditors and regulatory bodies as required.Provide practical quality and regulatory guidance to support compliance throughout the product lifecycle.Assist with audit readiness activities and support the organisation in preparing for upcoming regulatory and quality audits.About You To be successful, you will ideally have:Experience within the medical device industry, with exposure to Regulatory Affairs, Quality Assurance or both.Demonstrated EU MDR experience (essential).Experience supporting regulatory submissions, registrations and ongoing compliance activities.Knowledge of international medical device regulations, including TGA, EU MDR and ideally FDA and/or PMDA requirements.Experience maintaining technical documentation, technical files and quality system documentation.Familiarity with ISO 13485, MDSAP and medical device quality management systems.Experience supporting audits, quality system improvements and compliance initiatives.The ability to identify compliance gaps, assess risks and implement practical solutions.A hands-on, proactive approach with the ability to work independently in a small, collaborative team.Highly RegardedExperience with orthopaedic, surgical, sterile or software-enabled medical devices.Exposure to both Regulatory Affairs and Quality Assurance functions.Experience supporting global medical device registrations and interactions with Notified Bodies or regulatory authorities.Experience working within a small or growing MedTech organisation.Exposure to supplier audits, CAPA, risk management or post-market surveillance activities.Why Apply? This is more than a typical Quality & Regulatory role. You'll gain exposure across the full product lifecycle while working closely with Engineering, R&D and senior leadership in a growing medical device business. In this role, you'll gain exposure to:Global regulatory activities across Australia, Europe, Japan and the USA.Quality Management Systems, audit preparation and continuous improvement initiatives.Product design, development and commercialisation activities.Close collaboration with Engineering, R&D and Product Development teams.Supplier management, external audits and international compliance requirements.Manufacturing, sterilisation and distribution processes within a regulated medical device environment.Next-generation product development, including future AI-enabled technologies.Unlike larger organisations where responsibilities are heavily segmented, this role offers genuine ownership, variety and visibility. You'll work closely with an experienced Quality & Regulatory leader and have the opportunity to influence outcomes across the business while continuing to develop your technical expertise. What's on Offer?Competitive salary package.Hybrid working arrangements available following onboarding.Opportunity to join a growing Australian medical device company with products approved across Australia, Europe, Japan and the USA.Broad exposure across Quality Assurance, Regulatory Affairs, Engineering and Product Development.Opportunity to work on both hardware and software medical devices within a global regulatory environment.Significant ownership and visibility in a small, collaborative team.Exposure to future product development initiatives, including next-generation and AI-enabled technologies.Supportive leadership and the opportunity to work alongside highly experienced quality, regulatory and engineering professionals.Sydney Inner City location with excellent public transport access.Interested? If you are interested in this role, please submit your application and get in touch with Susan MacLeod at susan.macleod@evolvescientific.com.au.With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

About the role –A growing Australian engineering and technology company based in Melbourne, specialising in monitoring and industrial systems solutions.Based in the eastern suburbs of Melbourne. Short term casual contract with potential for extension Monday to Friday, 7am to 3pm. About your duties –Manufacture, assemble, integrate and test electronic and monitoring systems to engineering specifications.Read and interpret engineering drawings and technical documentation.Conduct functional testing, fault finding and troubleshooting activities.Assist with quality documentation, testing records and project reporting.Support factory acceptance testing alongside engineers and project teams.Maintain high standards of safety, quality and workshop housekeeping.Identify process improvements and provide feedback to support continuous improvement initiatives.Assist with packing and preparation of completed systems prior to customer delivery.About you –Certificate or qualification in Electronics, Electrical, Engineering or a related field 3-5 years experience in electronics, electrical assembly, systems integration, manufacturing, or a similar technical environment.Ability to read and interpret technical drawings and documentation.Strong fault-finding and troubleshooting skills.Hands-on experience with tools, testing equipment and assembly processes.Excellent communication skills and strong attention to detail.Ability to manage multiple tasks and work effectively within a team environment.Apply!If you think this could be the role for you then please apply now! Please send us a cover letter AND a detailed resume in WORD format (PDFs can be corrupted / not processed).  Or, if you have any questions, please contact Priyanka on 03 9040 1630.With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

About the role –Global Pharmaceutical Company in the Melbourne CBD area. An initial 3-month contract with potential of extension. Candidates must be flexible to work Monday to Friday on morning shift (start at 6:30/7 am) The role will be a 38-hour week with occasional overtime and weekend work.Standard 8-hour shifts.WHV with similar background encouraged to apply! Your duties -Packing of Pharmaceutical products along the production lineMaintaining and recording manufacturing documentationCleaning of manufacturing environment – rooms and equipmentMaintaining hygiene standards and aseptic techniquesAbout you –Strong understanding of GMP and cleanroom environmentsDemonstrated experience in a similar role within the Pharmaceutical/Medical devices industry. Preferable having experience in aseptic operations.Candidates must also be comfortable with aseptic gowning.Strong communication skillsKnack for quick learningGoes above and beyond.Apply! If you think this could be the role for you then please apply now! Please send us a cover letter AND a detailed resume in WORD format (PDFs can be corrupted / not processed).   Or, if you have any questions, please contact Priyanka on 03 9040 1630.With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

About the company/role:Well-established TGA governed radiopharmaceutical company based in BundooraSeeking a Microbiologist Assistant – full time position (8am – 4 pm)Permanent opportunityDuties:Environmental monitoringAseptic microbiological testingConduct Sterility testingPerform bioburden assessmentsPerform endotoxin testingData entryGeneral laboratory house keeping About you:Bachelor of Science majoring in Microbiology would be desirableDesired but not necessary, understanding of Good Manufacturing Practices (GMP)Excellent verbal and written communication skillsProven time management skills for planning and schedule of workYou will be a quality-focused individual with excellent attention to detail, be adaptable and have the ability to work in a close-knit team.Apply! If you think this could be the role for you then please apply now! Please send us a cover letter AND a detailed resume in WORD format (PDFs can be corrupted / not processed).   Or, if you have any questions, please contact Deborah on 03 9040 1630.With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

Our client is seeking a motivated and detail-oriented Payroll & Administration Officer to join their busy operations team. This is a fantastic opportunity for an experienced administrator who enjoys a varied role, thrives in a fast-paced environment, and is confident working across payroll support, data entry, invoicing, and operational administration. This is a 6-month casual assignment with the intention of transitioning to a permanent position for the right person.About the RoleWorking closely with the wider administration and operations team, you'll play a key role in supporting day-to-day business activities while ensuring payroll and job administration processes run smoothly.Key ResponsibilitiesSupport payroll processing activities, including timesheet validation and data entry.Ensure employee timesheets are accurately reviewed and processed each week.Monitor a shared inbox and action incoming job requests within required timeframes.Create and maintain job cards, ensuring information is entered accurately for quoting and invoicing purposes.Raise purchase orders and process invoices.Maintain accurate records and data across multiple systems.Provide administrative support across the business and assist with team coverage when required.Liaise with internal stakeholders to ensure operational tasks are completed efficiently.About YouTo be successful in this role, you will possess:Previous experience in an administration, payroll support, or similar coordination role.Excellent data entry skills and a high level of accuracy.Strong Excel skills and confidence learning new systems.Exceptional attention to detail and organisational skills.Strong communication skills and the ability to interact with people at all levels.A flexible, adaptable, and team-focused attitude.Previous experience within an industrial, construction, utilities, manufacturing, or service-based environment will be highly regarded.If you are an organised administrator who enjoys juggling multiple priorities, has strong attention to detail, and is looking for a long-term opportunity with a reputable organisation, we'd love to hear from you.Apply now or contact Steph at Evolve Scientific Recruitment for a confidential discussion.With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

PhD biologist role in radiopharmaceutical discoveryCell biology focus with pharmaceutical researchLucas Heights - government - Citizenship essentialPosition SummaryThe government organisation is a leader in the field of specialised life science research and is recognised world wide. Join a multidisciplinary team developing novel radiopharmaceuticals through cell-based research and biological evaluation of new therapeutic compounds.About the company/role:This position offers an exciting opportunity for an early-career scientist to contribute to the discovery and development of next-generation radiopharmaceuticals. Working at the interface of biology and chemistry, you will support the biological evaluation of novel compounds before they progress into preclinical development.The role is ideally suited to a PhD-qualified scientist with strong cell biology expertise and approximately 3-5 years of postdoctoral or industry experience. You will work closely with synthetic chemists and other researchers within a collaborative, multidisciplinary environment.Key Responsibilities:Perform mammalian and primary cell culture techniques.Conduct in vitro and ex vivo biological studies.Undertake flow cytometry and histology-based analyses.Perform ELISA, binding activity and cytotoxicity assays.Analyse and interpret experimental data.Support assay development, optimisation and validation.Collaborate closely with synthetic chemists on compound evaluation.Maintain accurate laboratory records and documentation.Work with radiolabelled compounds following radiation safety training.Contribute to research reports, presentations and project milestones.Skills/experience:Australian Citizenship status.PhD in Cell Biology, Molecular Biology, Biomedical Science, Pharmacology, Biochemistry or a related Approximately 3-5 years' postdoctoral or relevant industry experience.Strong hands-on experience with primary and/or mammalian cell culture.Experience conducting in vitro and/or ex vivo studies.Practical experience with flow cytometry and cell-based assays.Experience with ELISA, cytotoxicity assays and biological characterisation techniques.Understanding of chemistry gained through tertiary studies, research projects or industry experience desirableExposure to pharmaceutical development, translational research or radiopharmaceutical programs will be well regarded.Culture/Benefits:Please note: there is a 4-6 week security clearance after accepting an offer, so start date will be late Jan, early Feb 2027Pay rate $73.76 p/hr+super (includes casual loading)Opportunity to contribute to innovative radiopharmaceutical development programs.Collaborative multidisciplinary team environment.How to Apply:If you think this could be the role for you then please apply now! Please send us a cover letter and a detailed resume. Please include your Australian Citizenship status.With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

Machine Operator - Plastics Manufacturing (Night Shift) Location: Altona North Shift: Monday to Friday | 10:00pm - 6:00am Pay Rate: $48/hr + Super (inclusive of casual and night shift loading) Employment: Ongoing Casual with Full-Time Hours and Strong Potential for Permanent Employment About the Company Our client is a well-established Australian plastics manufacturer supplying products to a range of industries nationwide. Due to continued growth, they are seeking an experienced Machine Operator to join their night shift team. This position would suit candidates from plastics, packaging, food manufacturing, FMCG, extrusion, blow moulding, injection moulding, bottling, or automated production environments. Key ResponsibilitiesSet up, operate and monitor automated manufacturing machineryComplete machine changeovers and line adjustmentsTroubleshoot machine faults and perform basic mechanical adjustmentsIdentify and resolve production issues to minimise downtimeConduct quality inspections and investigate product defectsComplete routine cleaning and preventative maintenance tasksOperate a forklift to move raw materials and finished productsMaintain accurate production recordsFollow GMP, quality and safety proceduresAbout YouTo be successful, you'll have:Previous experience as a Machine Operator within a manufacturing environmentExperience operating automated production machineryStrong mechanical aptitude and the ability to troubleshoot equipment issuesExperience conducting machine set-ups, changeovers and adjustmentsA current LF Forklift Licence ideallyAbility to work autonomously on night shiftStrong focus on safety, quality and production performanceHighly RegardedPlastics manufacturing experienceBlow moulding experienceInjection moulding experienceExtrusion experienceFood, beverage or packaging manufacturing experienceApply! If you think this could be the role for you then please apply now! Please send us a cover letter AND a detailed resume in WORD format (PDFs can be corrupted / not processed).   Or, if you have any questions, please contact Chantelle on 03 9040 1630.With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

About the Company:Our client is a global leader in food ingredients and nutrition solutions, supplying products to some of the world's largest food and beverage manufacturers. With a strong focus on quality, innovation and food safety, they operate a highly regarded manufacturing facility in Moorebank, NSW and are seeking a Quality Control Assistant to join their laboratory team. This is an excellent opportunity for a Science graduate or early-career laboratory professional looking to build a long-term career within a quality-focused food manufacturing environment.About the Role:Reporting to the Quality Control Manager, you will support the day-to-day operations of the Quality Control Laboratory by performing routine testing, recording results, maintaining laboratory standards and assisting with quality investigations. You will play an important role in ensuring raw materials, in-process samples and finished products meet strict quality and food safety requirements before release. This position would suit someone with a background in Chemistry, Food Science, Microbiology, Biotechnology or a related scientific discipline who enjoys hands-on laboratory work and has strong attention to detail.Key Responsibilities:Perform routine laboratory testing on raw materials, in-process samples and finished productsPrepare samples, reagents, solutions and testing equipmentAccurately record and report laboratory resultsReview test results and identify out-of-specification resultsAssist in quality investigations and corrective actionsMaintain laboratory equipment and testing documentationSupport GMP, HACCP and quality compliance requirementsEnsure laboratory housekeeping and safety standards are maintainedAssist with laboratory inventory and consumable managementSupport continuous improvement initiatives within the quality functionAbout You:Degree qualification in Food Science, Chemistry, Microbiology, Biotechnology or a related disciplinePrevious laboratory or quality control experience within food, pharmaceutical or manufacturing environments (highly regarded)Strong attention to detail and analytical thinking skillsGood understanding of laboratory practices and quality systemsExcellent organisational and communication skillsAbility to work independently and as part of a teamStrong commitment to quality, food safety and workplace safetyDesirableGMP experienceHACCP knowledgeManufacturing laboratory experienceExposure to quality investigations and non-conformance managementExperience using laboratory equipment and testing methodsApply Now!If you think this could be the role for you then please apply now! Please send us a detailed resume in WORD format (PDFs can be corrupted / not processed).With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.