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In addition to Brazil, Minerva Foods operates in Paraguay, Argentina, Uruguay, Colombia, and has specialized sheep processing plants in Australia.\n\n\nWith our 46 industrial units, we offer healthy and nutritious products, distributed to customers worldwide through our 23 distribution centers and 17 international offices.\n\n **Responsibilities and duties** \n\nMonitor and oversee production processes, ensuring compliance with established quality standards;\n\n\nAssist in implementing Good Manufacturing Practices (GMP), HACCP and other self-control programs;\n\n\nParticipate in internal and external audits, collaborating in the preparation of documents and evidence;\n\n\nSupport employee training on quality, hygiene and food safety standards;\n\n **Requirements and qualifications** \n\n* High school diploma; technical education in production, quality, food technology or related fields is desirable.\n* Availability to work different shifts;\n\n **Additional information** \n\n* Health Insurance - With co-payment\n* Dental Insurance - With co-payment\n* Gympass/Wellhub (Gym membership)\n* Meal allowance\n* On-site meals\n* Local transportation\n\n \n\nThe leader in beef exports in South America, Minerva Foods is more than a global company – we are a community of professionals committed to \"creating connections between people, food, and nature.\" We operate in over 100 countries and have facilities in Brazil, Paraguay, Argentina, Uruguay, Colombia, and specialized sheep processing plants in Australia and Chile.\n\n \n\nWith solid management and innovative strategies, we constantly pursue the most promising markets, modernizing our operations and delivering high-quality products. Our integrated logistics and geographic diversification ensure solutions that meet the strictest global demands.\n\n \n\nAt Minerva Foods, sustainability is not just a commitment – it's part of our DNA. We adopt responsible practices that promote environmental preservation, animal welfare, and transparency throughout the entire production chain. Through robust traceability initiatives, we contribute to a more sustainable and transparent future.\n\n \n\nOur global impact is supported by 46 industrial units, 23 distribution centers, and 17 international offices. These pillars enable us to deliver healthy and nutritious products to customers around the world.\n\n \n\nIf you share values such as Results Orientation, Commitment, Sustainability, Innovation, and Recognition, join our team. 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Tiradentes, 32, Colina - SP, 14770-000, Brazil","infoId":"6433634982285112","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Laboratory Analyst","content":"Food Industry is hiring a Laboratory Analyst in Colina.\n\n**Responsibilities:**\nPerform physicochemical and microbiological analyses on raw materials, in-process products, and finished products to ensure food quality and safety. Conduct quality control tests, such as pH, moisture, fat content, among others, according to established procedures.\n\n**Compensation:*** Salary: To be determined.\n* Benefits: To be determined.\n\n**Additional Information:*** Employment Type: Permanent\n* Duration: Full-time\n* Work Schedule: 6×1 shift rotation.\n\n ***Work Location:*** *On-site in Colina / SP* \n\n***Application Deadline:*** *11/18/2025* \n\n***Expected Start Date:*** *11/26/2025* \n\n***JobId.:*** *29380468963* \n\n \n\n*✔ Follow:* ***@jobbol.empregos*** *on Instagram and get the best of the 2025 job market\\.*","price":"Negotiable Salary","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1762627733000","seoName":"laboratory-analyst","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://br.ok.com/en/city-barretos/cate-chemistry-physics/laboratory-analyst-6433634982285112/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"e704ee15-8686-4206-af2d-28d3a67c5bdf","sid":"baf29d1c-75d0-455a-b5da-10eac69db800"},"attrParams":{"summary":null,"highLight":["Conduct quality tests in food industry","Ensure product safety and quality","Full-time position in Colina / SP"],"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Colina,São Paulo","unit":null}]},"addDate":1762627732990,"categoryName":"Chemistry Physics","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"isFavorite":false},{"category":"4000,4374,4377","location":"R. 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We value teamwork, continuous improvement, and ethical patient care.\n\n\n**We have an opening for Occupational Safety Technician I** and we count on you to continue being part of this life-changing mission!\n\n\n\n**MAIN RESPONSIBILITIES AND DUTIES:**\n\n\n\nResponsible for implementing and monitoring workplace safety standards to prevent accidents and ensure employee health. Duties include conducting safety training, performing safety inspections of facilities, analyzing risks, and preparing reports on working conditions. The technician must also assist in implementing health and safety programs and promote employee awareness of safe practices.\n\n\n\n**REQUIREMENTS AND QUALIFICATIONS:**\n\n\n**Education:** Completed technical course in Occupational Safety | Registration with the competent body, which is the Conselho Regional de Engenharia e Agronomia (CREA) or specific professional council, depending on the qualification.\n\n\n**Desirable:** Additional certifications in specific occupational safety areas may be an advantage.\n\n\n**Requirements:** Previous experience in occupational safety activities, preferably in industrial or hospital environments;\n\n\n* Experience in developing and implementing occupational health and safety programs;\n* Knowledge of regulatory standards (NRs), especially NR 32, and occupational safety legislation;\n* Ability to conduct safety audits and inspections;\n* Familiarity with accident prevention and risk control procedures;\n* Knowledge of personal protective equipment (PPE) and collective protective equipment (CPE). 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Tiradentes, 32, Colina - SP, 14770-000, Brazil","infoId":"6414220125734712","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Veterinarians","content":"Veterinarian Position\nDescription:\nWe are seeking committed and qualified veterinarians to perform ante-mortem and post-mortem inspections of cattle, swine, and poultry, ensuring compliance with current legislation and protection of public health.\n\n \n\n\n\nResponsibilities:\n* Conduct ante-mortem and post-mortem inspections of cattle, swine, and poultry.\n* Ensure application of animal welfare, hygiene, and biosecurity standards;\n* Identify pathological changes and zoonoses;\n* Prepare official reports and records according to SIF/MAPA requirements;\n* Verify self-control programs and good manufacturing practices.\n\nRequirements:\n* Degree in Veterinary Medicine\n* Registration with the Regional Council of Veterinary Medicine (CRMV)\n* Previous experience in the field will be considered a plus\n* Ability to work in a team and handle emergency situations\n* Availability to work flexible hours, including weekends.","price":"Negotiable Salary","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1761110947000","seoName":"veterinary-doctors","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://br.ok.com/en/city-barretos/cate-food-technology-safety/veterinary-doctors-6414220125734712/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"f30e9334-b445-4a79-a3a2-c11e2a75383f","sid":"baf29d1c-75d0-455a-b5da-10eac69db800"},"attrParams":{"summary":null,"highLight":["Veterinary inspection of livestock","Ensure compliance with legislation","Report preparation for SIF/MAPA"],"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Colina,São Paulo","unit":null}]},"addDate":1761110947323,"categoryName":"Food Technology Safety","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"isFavorite":false},{"category":"4000,4374,4377","location":"R. 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Francisco Barreto, 99 - Centro, Barretos - SP, 14780-059, Brazil","infoId":"6382541853632312","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Clinical Research Assistant - Clinical Research (Barretos - São Paulo)","content":"**JOB DESCRIPTION**\n---------------------\n\n\n\nHow about joining the team of an institution whose core values are based on love and humanization?\n\n \n\nHospital de Amor has several hospital units, believes in its team, and continuously develops them, providing a positive organizational climate and well-being in the workplace.\n\n \n\nOur purpose is to provide services to patients of the Unified Health System in prevention, diagnosis, treatment, education, and oncology research.\n\n \n\nWe are looking for a professional for the role of **Clinical Research Assistant**.\n\n \n\nLearn more:\n\n\n\n**MAIN RESPONSIBILITIES OF THE POSITION**\n\n\n\nCollaborate with the study coordinator in managing and monitoring the study.\n\n\nSchedule exams according to protocols/medical requests.\n\n\nSchedule patient follow\\-ups in the system; issue the daily research schedule; verify medical records/system.\n\n\nPrepare all documentation for sending materials (biological samples and images) and schedule shipments.\n\n\nControl biological samples for storage and/or shipment.\n\n\nKeep the system updated by recording all patient\\-related activities (informed consent form signing; visits; exams; etc).\n\n\nReview each medical record, identify and/or request any pending exams, and archive them so that the record is complete for the medical consultation. If an exam is not ready, a note must be left on the front page of the record stating that it has been requested (date and time).\n\n\nCheck protocol material inventory and request restocking when needed.\n\n\nRequest results reports for radiological exams, ECGs, and other tests performed by study participants.\n\n\nSubmit requests to the pathology archive to separate the clinical research patient's material and retrieve it from the service. The material must be delivered immediately to the study coordination.\n\n\nArchive clinical study documents when delegated by the study coordinator.\n\n\nPerform other clinical research assistant duties as assigned within the study, in agreement and authorized by departmental coordination.\n\n\nSupport the completion of all sponsor platforms (CRF, IWRS, etc.) and resolve outstanding issues within established deadlines.\n\n\nWork in compliance with national and international clinical research guidelines and current regulations.\n\n\nInitiate first contact upon arrival of a new clinical study at the unit via the feasibility email.\n\n\nAssist the investigator in completing feasibility questionnaires together with the principal investigator and forward them to the respective sponsors.\n\n\nOrganize essential study documentation according to the initial study package along with the coordinator when required, concluding the start\\-up/regulatory process.\n\n\nCarry out the preparation of center documents for each study, ensuring they follow the initial submission to the CEP/CONEP system.\n\n\nPrepare and submit protocol amendments to CEP/CONEP, as well as notifications, safety reports, and other documents required by the study.\n\n\nResponsible for obtaining written and dated favorable approval opinions from CEP for the study protocol, investigator’s brochure, informed consent form, updates to the informed consent form, patient recruitment procedures (e.g., published advertisements), and all other information to be provided to the patient in the study.\n\n\nSupport qualification site visits by responding to monitors’ and/or managers’ inquiries and presenting the hospital and its facilities.\n\n\nEstablish direct communication with the Ethics Committee (CEP) regarding research protocols, assist in resolving ethical issues in coordination with sponsors, and provide CEP with all research documents subject to ethical review.\n\n\nRespond to questions raised by sponsors throughout the entire start\\-up phase of the research protocol.\n\n\nWork in compliance with national and international clinical research standards and current regulations.\n\n\nParticipate in all Site Initiation Visits (SIV), post\\-SIV meetings, multidisciplinary meetings, departmental meetings, meetings with investigators and sponsors, recruitment meetings, and training sessions.\n\n\nAttend meetings with sponsors when summoned.\n\n\nManage corporate email and recruitment.pesquisaclinica@hcancerbarretos.com.br.\n\n\nDevelop, implement, and analyze recruitment strategies tailored to each clinical study to identify potential candidates.\n\n\nIdentify, monitor, and flag potential candidates for clinical studies in the TASY system and physically on the patient’s card, as well as perform double\\-checking of eligibility criteria when flagged by another team member.\n\n\nFollow up with specialties in the outpatient clinic, assisting in the selection of new patients.\n\n\nCommunicate and coordinate processes with supporting research departments such as pathology, molecular biology, oncogenetics, radiotherapy, interventional radiology, among others, whenever necessary.\n\n\nAssist the coordination team and medical staff with scheduling and signing Informed Consent Forms (ICFs) and others when needed.\n\n\nDevelop facilitative tools for clinical studies for internal and external dissemination.\n\n\nCreate, manage, and share internal announcements, brochures, informational bulletins, folders containing current eligibility criteria and active ICFs, aiming to keep the medical team constantly updated on open clinical studies for recruitment.\n\n\n\nManage and disseminate monthly data to the medical team through an informational bulletin.\n\n\nManage WhatsApp groups for each specialty with internal physicians and those from other Hospital de Amor (HA) units such as Jales, Porto Velho, Campinas Prevention Unit, among others, aiming to strengthen communication and sharing of updated clinical protocol information.\n\n\nGuide medical residents in recruiting potential candidates for clinical studies according to eligibility criteria.\n\n\nConduct monthly recruitment indicator assessments, analyze them, and report findings to the Clinical Research Department.\n\n**REQUIREMENTS AND QUALIFICATIONS**\n\n\n* High school diploma completed\n* Preferably a student in the healthcare field\n* Basic English proficiency desirable\n* Proficiency in Microsoft Office\n* Computer skills\n\n**WORK HOURS**\n\n\n\nFrom 08:00 to 18:00, Monday to Friday.\n\n \n\n\n \n\n\n### **Employment Type:**\n\n\nCLT\n\n### **Benefits:**\n\n\nBasic Food Basket, Meal Allowance, Transportation Allowance, Medical Assistance, Pharmaceutical Discount Program, Gym Access\n\n### **Department:**\n\n\nAdult Oncology Hospital \\- Barretos \\- São Paulo","price":"Negotiable Salary","unit":"per 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Francisco Barreto, 99 - Centro, Barretos - SP, 14780-059, Brazil","infoId":"6382541762521712","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Clinical Research Assistant – Clinical Research (Barretos – São Paulo)","content":"JOB DESCRIPTION\n\nWhat if you could join the team of an institution whose core values are based on love and humanization?\n\n\n\nHospital de Amor has several hospital units, believes in its team and continuously develops them, providing a positive organizational climate and well-being in the workplace.\n\n\n\nOur purpose is to provide services to patients of the Unified Health System in prevention, diagnostics, treatment, education, and oncology research.\n\n\n\nWe are looking for a professional for the position of **Clinical Research Assistant**.\n\n\nLearn more:\n\n\n\n\n\n**MAIN RESPONSIBILITIES OF THE POSITION** ;\n\n\n\n;Work in compliance with national and international clinical research regulations and current resolutions. ;\n\n\n\nCollaborate with the study coordinator in managing and monitoring the study.\n\n\nSchedule exams according to protocols/physician requests.\n\n\nSchedule patient follow\\-ups in the system; issue the daily research schedule; verify medical records/system.\n\n\nPrepare all documentation for sending materials (biological samples and images) and schedule shipments.\n\n\nControl biological samples for storage and/or shipment.\n\n\nKeep the system updated by recording all patient\\-related activities (informed consent signing; visits; exams; etc);\n\n\nReview each medical record, identify and/or request pending exams, and file them so that the medical record is complete for the physician consultation. If any exam is not ready, a note must be placed on the front page of the record stating that the exam was requested (date and time).\n\n\nCheck protocol material inventory and request replenishment.\n\n\nRequest results reports for radiological exams, electrocardiograms, and other tests performed by study participants.\n\n\nSubmit requests to the pathology archive to separate the clinical research patient's material and retrieve it from the service. The material must be delivered immediately to the study coordination.\n\n\nFile clinical study documents when delegated by the study coordinator.\n\n\n;Prepare cover sheets for fax, mail, correspondence, and submissions to the Ethics Committee (CEP) and forward them to the responsible person for review and signature. ;\n\n\n\nPerform other clinical research assistant duties as assigned within the study, in agreement and authorized by department coordination.\n\n\n;Manage expense reimbursements for study participants, such as meals, accommodation, and transportation, together with the start\\-up team. ;\n\n\n\n;Fill out all internal spreadsheets as required by the center along with the study coordinator ;\n\n\n\nSupport the completion of all sponsor platforms (CRF, IWRS, etc.) and resolve outstanding issues within established deadlines.\n\n\nWork in compliance with national and international clinical research regulations and current resolutions.\n\n\nInitiate first contact upon arrival of a clinical study at the unit via the feasibility email.\n\n\nAssist the investigator in completing feasibility questionnaires with the principal investigator and forward them to the respective sponsors.\n\n\nOrganize essential study documentation according to the initial study package with the coordinator when required, concluding the start\\-up/regulatory process.\n\n\nCarry out the preparation of center documents for each study, which must be followed by initial submission to the CEP/CONEP system.\n\n\nPrepare and submit protocol amendments to CEP/CONEP, as well as notifications, safety reports, and other documents required by the study.\n\n\nResponsible for obtaining written and dated favorable approval or opinion from the CEP for the study protocol, investigator's brochure, informed consent form, updates to the informed consent form, patient recruitment procedures (e.g., published advertisements), and all other information to be provided to the patient in the study.\n\n\nSupport the Center Qualification Visit, responding to monitor and/or manager inquiries and presenting the hospital and its facilities.\n\n\nEstablish direct communication with the Ethics Committee (CEP) regarding research protocols, assist in resolving ethical issues with sponsors, and provide the CEP with all research documents subject to ethical review.\n\n\nRespond to questions raised by sponsors throughout the entire start\\-up phase of the research protocol.\n\n\nWork in compliance with national and international clinical research regulations and current resolutions.\n\n\nParticipate in all Initiation Visit meetings (SIV), post\\-SIV meetings, multidisciplinary meetings, departmental meetings, meetings with the investigator and sponsor, recruitment meetings, and trainings.\n\n\nAttend sponsor meetings when summoned.\n\n\nManage corporate email and recrutamento.pesquisaclinica@hcancerbarretos.com.br.\n\n\nDevelop, implement, and analyze recruitment strategies according to each clinical study to identify potential candidates.\n\n\nIdentify, track, and flag potential candidates for clinical studies in the Tasy system and physically on the patient's card, as well as perform double verification of eligibility criteria when flagged by another team member.\n\n\nFollow up with specialties in the outpatient clinic, assisting in the selection of new patients.\n\n\nCommunicate and interact with supporting research departments such as pathology, molecular biology, oncogenetics, radiotherapy, interventional radiology, among others, whenever necessary.\n\n\nAssist the coordination team and medical staff with scheduling and signing Informed Consent Forms (ICF) and others when needed.\n\n\nCreate facilitative tools for clinical studies for internal and external dissemination.\n\n\nDevelop, manage, and share internal announcements, brochures, informational bulletins, folders with current eligibility criteria and active ICFs, aiming to keep the medical team constantly updated on open clinical studies for recruitment.\n\n\n\nManage and disseminate monthly data to the medical team through an informational bulletin.\n\n\nManage WhatsApp groups for each specialty with internal physicians and those from other Hospital de Amor (HA) units such as Jales, Porto Velho, Campinas Prevention Unit, among others, aiming to strengthen communication and updated information on clinical protocols.\n\n\nGuide medical residents in recruiting potential candidates for clinical studies according to eligibility criteria.\n\n\nConduct monthly recruitment indicators assessment, analyze, and disseminate to the Clinical Research Department.\n\n\n;Perform review/update of Recruitment Standard Operating Procedures (SOP). ;\n\n\n\n**REQUIREMENTS AND QUALIFICATIONS**\n\n\nHigh School Diploma Required; 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