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About the role:Major pharmaceutical companyBased in the Eastern suburbs of Melbourne Looking for a Validation Associate to join the team3-month casual contract (potential to extend)Monday to Friday, full time hoursImmediate startOpen to Working Holiday Visas and engineering graduates with experience in equipment qualification About your duties:Execute validation activities across equipment (e.g. tanks, pumps, filling machines, incubators) in alignment with Validation Master Plans and regulatory requirementsDevelop and review qualification and validation documentation in accordance with compliance requirements and project timelinesProvide oversight of the sites quality systems and compliancePerform real time review of records concurrent with manufacturing, QC, or warehouse operations on the floorSupport the development, revision and implementation of SOPs, protocols, and other GMP documentsConduct internal audits to verify adherence to quality systems and support external regulatory inspectionsCollaborate with internal and external stakeholders About you: Tertiary education in Science, Engineering or Pharmaceutical ScienceProven experience in validation to support equipment qualification activities for manufacturingMust have prior experience within nutraceutical, cosmetic and/or pharmaceutical manufacturingExcellent communication skills, detail oriented and team collaboration 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 Linda 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: Our client, a global environmental organisation, is currently seeking a Mechanical Project Engineer to join their team at the Gold Coast Desalination Plant. This is a long-term casual contract role with full-time hours each week. As a Project Engineer, you will be responsible for initiating and delivering mechanical engineering projects from concept through to completion. Working closely with operations, maintenance, procurement and asset management teams, you will ensure projects are delivered safely, on time and within budget while supporting the ongoing performance and reliability of a major water treatment facility. Duties:Plan and deliver mechanical engineering projects through the full project lifecycle.Prepare detailed project scopes, technical documentation, schedules and cost estimates.Deliver assigned projects within budget and agreed timeframes while ensuring safe execution across all phases.Liaise with operations, maintenance, procurement and asset management teams to support successful project delivery.Coordinate tender site visits, prepare purchase orders and manage procurement activities.Manage subcontractors and engineering consultants, including site supervision and technical oversight.Review and approve contractor progress claims and invoices.Manage project budgets, schedules and reporting.Ensure project documentation, drawings, operational procedures and O&M manuals are updated and maintained.Ensure all project activities comply with relevant WHS, environmental, quality and site-specific requirements. Skills/experience:Bachelor's degree (or equivalent) in Mechanical Engineering.Registered Professional Engineer of Queensland (RPEQ) in the Mechanical area of practice, or eligibility to obtain RPEQ within an agreed timeframe.Post-graduate experience delivering projects within water, desalination, oil & gas, process plant or similar heavy industrial environments.Demonstrated experience with mechanical systems including pumps, piping, pressure equipment or process plant infrastructure. Experience with reverse osmosis or membrane-based water treatment is highly regarded.Strong knowledge of relevant Australian Standards, the National Construction Code and Queensland WHS legislation.Experience managing contractors, consultants, project budgets and schedules. 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).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:Join a leading pharmaceutical organisation supporting automation and manufacturing operations within a highly regulated environment.Seeking an experienced Automation Engineer to provide technical expertise across automated manufacturing systems and projects.12-month contract opportunity with strong potential for extension.Melbourne-based role offering the opportunity to work on a range of automation initiatives within pharmaceutical manufacturing.Duties:Your responsibilities may include but are not limited to:Support the implementation, maintenance and continuous improvement of automated manufacturing systems.Provide technical support for automation-related projects and operational activities.Collaborate with cross-functional teams to deliver automation solutions that meet business and operational requirements.Assist with system testing, commissioning, qualification and validation activities.Prepare and review technical documentation and engineering specifications.Ensure automation systems operate in accordance with quality, safety and regulatory requirements.Troubleshoot automation issues and support ongoing system optimisation initiatives.About You:Bachelor's degree in Engineering, Automation or a related discipline is preferred.Previous automation engineering experience within a pharmaceutical manufacturing environment is essential.Experience working with automated manufacturing and control systems.Understanding of GMP environments and regulated manufacturing practices.Knowledge of automation system lifecycle management and validation principles.Strong problem-solving and troubleshooting abilities.Excellent communication and stakeholder management skills.Ability to work independently and collaboratively within multidisciplinary teams.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.

AAbout the company/role:Growing and innovative agricultural-based companyPermanent, full-time opportunity for a Production Supervisor to oversee and actively participate in the day-to-day manufacturing of their unique and sustainable productsImmediate startFulltime hours, Monday-FridayDay shift Key responsibilities include:Supervise daily production operations, ensuring efficient, safe, and high-quality outputCoordinate production schedules to meet customer orders and delivery deadlinesLead, train, and support production staff, fostering productivity, teamwork, and safe work practicesConduct daily toolbox talks and communicate operational priorities and performance expectationsOperate and oversee production equipment, including mixers, pumps, tanks, transfer systems, and forkliftsMonitor blending, batching, packaging, and quality control processes, including pH, density, and batch testingAssist with raw material handling, inventory management, stock takes, and reporting material shortagesMaintain production areas, perform equipment cleaning, and troubleshoot minor operational issues to minimise downtimeEnsure compliance with WHS, environmental, chemical handling, and quality assurance requirementsCoordinate preventative maintenance activities and collaborate with maintenance and logistics teams to optimise operational efficiency Skills & experience required:Previous experience in fertiliser, chemical, agricultural or industrial manufacturing environmentDemonstrated supervisory or team leadership experienceStrong mechanical aptitude and willingness to work hands-onMust have a forklift license and able to operate other production equipmentGood OH&S understanding and practicesStrong communication and oranisational skillsGood computer skills for production reporting and inventory systems 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 Linda 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 CompanyOur client is a leading global biopharmaceutical organisation committed to developing and delivering innovative therapies that improve and save lives worldwide. With a strong focus on quality, compliance and continuous improvement, they operate state-of-the-art manufacturing and quality facilities supporting critical healthcare products.This role is based in Broadmeadows, Melbourne.About the RoleWe are seeking an experienced Senior Associate, Quality Engineering to join a dynamic Engineering and Quality team on an initial 12-month contract. The successful candidate will be responsible for providing quality engineering support across engineering, commissioning, qualification and validation activities, ensuring compliance with GMP and quality requirements while supporting project delivery.Key ResponsibilitiesReview and approve engineering documentation.Review commissioning, qualification, validation and stability documentation. Provide quality oversight and support throughout qualification activities. Escalate quality and compliance issues and provide recommendations on appropriate next steps. Support project teams to ensure engineering and quality requirements are met. Ensure documentation and processes comply with GMP and regulatory expectations.Work collaboratively with Engineering, Quality Assurance and project stakeholders. Must HaveDegree in Life Sciences, Pharmaceutical science, Engineering or a related discipline. Advanced degree highly regarded.Minimum 3 years' experience in a similar Quality Engineering role within the pharmaceutical industry.Previous technical experience in engineering, commissioning and qualification. Strong understanding of Quality Assurance, GMP compliance and quality systems. Demonstrated independent problem-solving abilities. Excellent attention to detail and documentation review skills.Apply!Click the Apply Now button with a cover letter addressing the selection criteria above AND a detailed resume in WORD format (PDFs can be corrupted/not processed).For more information, please contact Linda 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: Our client, a leading pharmaceutical manufacturing company, is seeking a Packaging Operator to join their production team. This is an excellent opportunity to work within a highly regulated manufacturing environment, supporting the packaging of pharmaceutical products while ensuring quality, safety, and GMP standards are maintained. You will be joining a supportive, collaborative team with ongoing training and development opportunities. The successful candidates must be able to work rotating (morning and afternoon) shifts and complete a full medical and criminal history check. Duties:Set up and operate packaging machinery, including blister pack, bottle, carton, and labelling equipment.Monitor production lines and make basic machine adjustments as required.Pack, inspect, and label pharmaceutical products in line with quality standards.Complete production paperwork and enter data into company systems.Identify machine faults, product defects, and production issues, reporting them to supervisors as required.Follow daily production schedules and meet team targets.Maintain a clean, organised, and safe work area.Follow GMP, SOP, and workplace health and safety requirements at all times.Work closely with team members to keep production running smoothly.Skills/Experience:Previous experience in manufacturing, production, packaging, warehouse, or machine operation roles.Experience working with automated or semi-automated machinery is highly regarded.Mechanically minded with the ability to troubleshoot basic equipment issues.Strong attention to detail and commitment to quality.Ability to follow procedures and complete documentation accurately.Reliable with a strong work ethic and positive attitude.Comfortable working in a fast-paced production environment.Ability to work rotating shifts.Physically fit and capable of being on your feet for extended periods.Culture & Benefits:Join a well-established global pharmaceutical company.Full training provided.Stable, long-term employment opportunities.Supportive team environment and strong safety culture.Opportunities for career progression and internal development.Modern manufacturing facility with onsite amenities.Employee recognition programs and performance rewards.Work for a company committed to continuous improvement and employee development.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 Raine on (07) 3175 0680.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.

Lead Clinical Research CoordinatorMelbourne, VIC | Full-TimeEvolve Scientific is partnering with a leading clinical research organisation to recruit a Lead Clinical Research Coordinator. This role is ideal for an experienced Registered Nurse or Pharmacist looking to combine hands-on clinical trial coordination with team leadership and site oversight.Key ResponsibilitiesLead the delivery of clinical trials from start-up through to close-out.Coordinate participant recruitment, screening, enrolment, and follow-up.Ensure compliance with study protocols, GCP, and regulatory requirements.Maintain accurate study documentation and data quality.Liaise with investigators, sponsors, CROs, and key stakeholders.Support site operations, mentor staff, and drive process improvements.About YouAHPRA-registered Nurse or Pharmacist.Proven experience coordinating clinical trials.Strong understanding of GCP and clinical research regulations.Excellent organisational, communication, and stakeholder management skills.Previous leadership or mentoring experience highly regarded.What's on OfferOpportunity to step into a clinical research leadership role.Exposure to a diverse portfolio of studies and therapeutic areas.Supportive, collaborative team environment.Professional development and career progression opportunities.Join a high-performing research team and play a key role in advancing innovative healthcare treatments. Apply through Evolve Scientific today.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:This role is with Seqirus based in Tullamarine, Melbourne offering a hybrid working model (3 days onsite). Seeking a Senior Validation Specialist (QC Microbiology) to provide SME leadership across method validation, method development, troubleshooting, and continuous improvement activities. 12-month casual contract with potential for extension.Opportunity to work on innovative microbiology and analytical testing technologies within a highly regulated GMP environment. Duties: Your responsibilities may include but are not limited to:Maintain the compliant status of the QC method validation lifecycle.Lead technical investigations and troubleshooting activities for QC test methods, including CAPA and Change Control actions. Provide SME oversight for method standardisation and robustness programs.Develop, optimise and validate new and existing microbiological and analytical test methods. Lead and coordinate method transfer activities across sites. Support regulatory filings, audits and inspection readiness activities. Design and execute validation studies involving new technologies and QC processes. Review validation data, identify trends or deviations and escalate findings where required.Maintain awareness of emerging industry technologies, equipment and best practices. About You:Bachelor’s degree in Microbiology, Biochemistry, Life Sciences or a related discipline. Strong microbiology and/or biochemistry background within a pharmaceutical, biotechnology, biologics or vaccine environment. Demonstrated experience in method validation, method development and method transfer activities. Strong understanding of GMP, quality systems, CAPA, deviations and Change Control processes. Proven troubleshooting and problem-solving capabilities within a QC laboratory environment. Experience supporting regulatory inspections and audits highly desirable. Experience with plate reader software would be advantageous. Excellent communication, stakeholder management and project coordination skills.Ability to work independently while providing technical leadership and guidance to others.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.