Pharmaceutical & Biotechnology

I'm partnering with a diagnostics company in Malaysia in search for a Product Manager who would be responsible for managing and growing the medical diagnostics product portfolio with a strong focus on the pharmacy channel in Malaysia. This role drives product strategy, commercialization, and market penetration for diagnostic products distributed through retail pharmacy chains and independent pharmacies. The role works closely with sales, marketing, and regulatory teams to expand product reach and strengthen brand presence in the local consumer healthcare market. Key ResponsibilitiesManage and develop the medical diagnostics portfolio across pharmacy channels in MalaysiaDevelop and execute product strategies aligned with retail healthcare and consumer diagnostics trendsDrive go-to-market plans including product positioning, pricing strategy, and channel activation within pharmacy networksSupport product launches and ensure strong market penetration across pharmacy chains and independent pharmaciesWork closely with sales teams and distributors to achieve sales targets and expand pharmacy channel coverageBuild and maintain relationships with pharmacists, pharmacy chain buyers, and key retail healthcare stakeholdersConduct market research to identify trends in self-testing, point-of-care diagnostics, and consumer-driven healthcare behaviourProvide product training and sales support materials to internal teams and external partnersCollaborate with regulatory, supply chain, and marketing teams to ensure product availability and compliance with local requirementsMonitor sales performance, channel performance, and competitor activity to drive continuous improvementRequirementsBachelor’s degree in Life Sciences, Biomedical Science, Pharmacy, Biotechnology, or related field3–6 years of experience in product management or marketing within medical diagnostics, IVD, or healthcare productsStrong understanding of pharmacy retail channel dynamics in Malaysia is highly desirableRegistration Number: R24123122With 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:Join a Leading Veterinary Pharmaceutical Company who specialise in the development and manufacturing of veterinary medicines. This is your chance to be part of a team committed to excellence and innovation.About the Role:As a QC Laboratry Technician, you will report to the QC Operations Lead and work in a laboratory based, site environment. You will play a critical support role in the Quality Control function by coordinating and performing sampling activities, maintaining accurate records, and ensuring materials and products are handled in accordance with GMP and regulatory requirements. This role is well‑suited to candidates with a strong attention to detail who enjoy structured, hands‑on laboratory work and are looking to build or consolidate their experience in a pharmaceutical manufacturing setting.  Duties:Collect and coordinate samples across materials, production stages, and monitoring programs in line with schedules and proceduresReceive, inspect, label, and log samples with full traceabilityPrepare samples for in‑house analysis and external testingMaintain accurate laboratory records, logs, and system entries; escalate deviations as requiredSupport in‑process checks and routine physical testing alongside QC and Production teamsMaintain laboratory areas, sample booths, equipment, and glassware to required standardsManage retention/reference samples, consumables, reagents, and inventoryAssist with routine equipment checks, calibration, and verificationOperate in compliance with GMP/GLP, safety, and regulatory standards Skills & Experience:Diploma or Bachelor in Laboratory Technology, Science, Pharmaceutical Science, or similarBackground in laboratory, manufacturing, or quality environments; regulated experience highly regardedStrong SOP adherence with accurate documentation skillsKnowledge of basic laboratory techniques and sample handlingHigh attention to detail with a compliance‑focused mindsetConfident using Microsoft Office and laboratory systemsTeam‑oriented with the ability to manage routine tasks independentlyCulture & Benefits:Free on-site parking for your convenienceOngoing training and professional developmentClear career progression opportunitiesBe part of a high-performing, supportive team that values collaboration and innovation Please Note: A police check and pre-employment medical (including drug and alcohol screening) are required prior to commencement. These will be organised by the company. Apply Now!Ready to take the next step in your career? Submit your application today!Please include a detailed resume in Word format (PDFs may not process correctly)For any questions about the role, contact Mairead on  61 2 8071 4290.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 health company in the Melbourne CBD.12 month permanent opportunityCandidates must be flexible to work between the hours of 7.30am and 4pm. The role will be a 38-hour week with occasional overtime and weekend work.Standard 8-hour shifts.Your duties:Preparation and approval of new GMP documentationParticipate in all GMP audits for new products and perform follow up actions as neededEstablish training requirements for production staff for new and changed processesSolution preparationsPerform commissioning, qualification and validation tasks as neededParticipate in all GMP audits for new products and perform follow up actions as neededPlant and equipment cleaning and sterilizationMonitoring of cultures in small & large scale bio-reactorsDownstream processing and purification of antigensImplement training plans to ensure smooth introduction of new products and processesProvide technical assistance for manufacturing operations for new processes About you:Strong understanding of GMP and cleanroom environmentsTertiary qualification in Microbiological Science, Engineering or related discipline is desirableDemonstrated experience in a similar role within the Pharmaceutical/Food industry.Strong communication skillsKnack for quick learningGoes above and beyondApply! 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 or Sarah 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, a reputable packaging organization, is experiencing rapid growth. They specialize in manufacturing packaging products for the Food and Dairy industry and are committed to delivering high-quality solutions to their customers. Due to continued expansion, they are currently seeking a Die Setter to join their thriving team on a casual full-time basis. This role is based in the Southeastern suburbs of Melbourne and operates Monday to Friday, 7:00am to 3:00pm. About the role: We are currently seeking a skilled and reliable Die Setter to support our client's production operations. Reporting directly to the Operations Manager, this role is responsible for setting up and maintaining molds (dies) in plastic manufacturing machines to ensure smooth and efficient production. This is a hands-on role that requires mechanical aptitude, attention to detail, and a proactive approach to problem-solving. Duties will include but are not limited to:Installing and removing molds (dies) in injection molding machinesPerforming machine setup and calibration to meet production specificationsConducting trial runs and quality checksTroubleshooting molding issues and adjusting machine parametersPerforming routine maintenance and minor repairs on diesCollaborating with production and quality teams to meet output targetsEnsuring safety and compliance with operational proceduresTo be successful in this position you will have:Previous experience as a Die Setter or in a similar role within plastics or manufacturingStrong mechanical aptitude and understanding of molding processesAbility to read and interpret technical drawingsExcellent problem-solving and troubleshooting skillsGood communication and teamwork abilitiesForklift license desirable but not essentialCommitment to safety and quality standardsApply! If you think this could be the role for you, then please apply now! 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 well-established veterinary pharmaceutical company which develops products for livestock, poultry and companion animals. About the role: This is a hands-on QC Chemist role focused on HPLC testing, supporting routine quality control and stability programs within a small team. Duties:Perform HPLC and UPLC analysis on finished productsConduct stability and finished product testingCarry out wet chemistry testing including pH, titration, and viscosityPrepare reagents and maintain laboratory equipmentMonitor stock levels and maintain lab inventoryRaise out of specification reports and change controlsMaintain accurate documentation (paper-based and electronic systems)Support general lab operations including cleaning and ad hoc tasks Skills/experience: Essential: Industry HPLC experience in a GMP-regulated lab (pharma or veterinary)Bachelor of Science degree majoring in Chemistry or equivalent qualification.Experience performing assay and finished product testingHands-on wet chemistry experience (titration, pH, viscosity)Experience raising OOS, deviations, and change controlsExposure to QMS/cQMS systemsConfident working independently and managing own testing workloadMinimum 2 years in a QC laboratory preferred Benefits:Early finish Fridays (2:30pm, paid full day)Flexible start times (7:30am–8:30am) 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 Priangel on 0406 558 313 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:Major pharmaceutical companyBased in the Northern suburbs of MelbourneJoin the team as a Plasma Scanning Operator working within a fast-paced warehouse environment focused on the safe and accurate handling and scanning of plasma unitsRoutine, repetitive, and manual, requiring strong attention to detail and the ability to work autonomouslyCasual contract, full time hours (Mon-Fri)Multiple positions available across day and afternoon shifts Duties will include, but not limited to:Request and remove pallets of plasma via the internal systemOperate walkie stacker to safely move packagesTransfer units from conveyor to pallet conveyorEmpty pallet contents onto the scanning tableScan each plasma unit, place into crates, and return crates to conveyorAssist with repalletising and returning completed pallets to the freezerComplete documentation for any rejected or problematic unitsMaintain general housekeeping and follow all safety procedures  Skills/experience required:Prior work experience in a warehousing, pick/packing, or RF scanning environmentPrior pharmaceutical manufacturing experience (advantageous)Current forklift license (advantageous)Strong attention to detailAbility to perform repetitive and manual tasks - lift upto 12kgAbility to work independently and maintain focusReliability, consistency, and a commitment to qualityWillingness to learn and follow established processes 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.

We are seeking a Clinical Research Associate (CRA) to support an oncology clinical study in Hong Kong.Location: Hong Kong Full-TimeThis role involves monitoring, site management, and regulatory compliance to ensure study integrity and patient safety. Key Responsibilities:Conduct site visits, monitoring, and data verification.Ensure compliance with GCP, protocols, and regulatory requirements.Collaborate with investigators and site staff to ensure study progress.Maintain accurate documentation and reporting.Requirements:Degree in life sciences or related field.2 years of CRA experience (oncology preferred).Strong knowledge of GCP and regulatory guidelines.Fluent in Mandarin and/or Cantonese (spoken and written).Excellent communication and organizational skills.Apply now to be part of an impactful oncology research team!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 pharmaceutical company seeking a Documentation/Quality Specialist to join their team6-month contractOnsite, full-time hours (Mon-Fri)Normal business hours Based in South Eastern suburbs Duties, but not limited to:Develop and evaluate quality and system procedures to ensure reliability, usability and complianceWrite procedural documentation such as SOPs, work instructions and formsCollaborate with internal teams across departments and liaise with SMEs to extract informationReview batch release documentationReview/approval revalidation and requalification reports and documentationAdministration and maintenance of Quality Management SystemsPerforming visual inspections on intermediate and finished productsAssist in the preparation of summary protocols and batch release documentationLiaising with both internal and external stakeholders Skills/experience:Tertiary education in a relevant science discipline (Chemistry, Biochemistry, Pharmaceutical, Biology or similar)3 years in a GMP environment within pharmaceutical, biotech or other highly regulated environmentDemonstrated experience working as a Quality Associate/Validation Associate within a GMP environmentKnowledge of TGA, FDA, EMA requirementsGood interpersonal, analytical and problem-solving skillsAbility to work well independently and in a teamGreat organisational and time management skills 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 Sarah 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.