209 Jobs in the Buenos Aires: The Ultimate Buyers Guide (2025)

Grain Receiving Inspector64704922682242120

**Company Description** Louis Dreyfus Company is a global leader in the marketing and processing of agricultural products. Our activities span the entire value chain—from farm to fork—across a broad range of business lines. Leveraging our global reach and extensive asset network, we serve our customers and consumers worldwide. Structured as a matrix organization comprising six geographic regions and ten platforms, Louis Dreyfus Company operates in over 100 countries and employs approximately 18,000 people globally. **Job Description** * Receives grain samples and conducts analyses according to established standards for grain trading to determine the quality of goods entering the Plant. * Based on the analyses performed and the type of grain, determines the quality grade of the goods. Analysis results are recorded in the Loading/Unloading System to classify incoming goods at the facility, implement appropriate measures as needed, and inform relevant personnel and entities. * Enters information into the system and prints the sampling ticket so that departments involved in the truck loading/unloading process can access the information obtained in the Sampling Department. * Controls equipment and tools required for routine measurements and reports any issues to verify the condition of tools and equipment, ensuring proper sampling and accurate analysis while minimizing errors. * Understands and complies with the Statutory Bases and Standards set by the Cereal Arbitration Chamber, using these bases as benchmarks to assess grain quality and standardize decision-making criteria. * Adheres to daily operational guidelines established by the supervisor to ensure coordinated execution of all operations, guaranteeing timely availability of goods in the right quantity and quality. * Reports daily operational updates from their area to the Procurement Manager to maintain an appropriate flow of information. * Complies with regional policies regarding quality, safety, hygiene, and asset management. **Requirements** * Completed secondary education. * Certification as a Grain Receiving Inspector. * Proven experience in grain procurement facilities. **Additional Information** Residence in the area or willingness to relocate. **What We Offer** A multicultural, dynamic, and challenging environment that will broaden and develop your capabilities, channel your skills and experience through excellent professional development opportunities within one of the world’s most robust companies. These are some of our benefits: * Competitive salary and benefits. * Flexible work environment. * Access to training and development programs. * Health and wellness program. * Extended maternity and paternity leave. **Diversity & Inclusion** LDC is guided by a set of shared values, high ethical standards, and diversity and inclusion are integral to our DNA. LDC is an equal opportunity employer committed to fostering a workplace that embraces and values diversity, equity, and inclusion. LDC promotes diversity, supports local communities, and environmental initiatives. We encourage individuals from all backgrounds to apply. **Sustainability** Sustainable value lies at the core of our corporate purpose. We are passionate about creating fair and sustainable value—not only for our company but also for all stakeholders across the value chain: our people, our business partners, the communities we engage with, and the environment surrounding us.

los paraisos 1010, B2942 Baradero, Provincia de Buenos Aires, Argentina

Negotiable Salary

Indeed

Caregivers - Baradero

At Grupo Medihome, we are currently seeking Home Caregivers to care for patients requiring home hospitalization in Baradero, Buenos Aires Province. We are looking for caregivers residing in the area or nearby, who have experience in caring for elderly adults, young adults, or pediatric patients. We request that you complete all fields when applying and/or attach your updated CV. Requirements To join our team as a caregiver, it will be necessary to: Have active monotributo registration or the ability to process it. Reside in the area or be able to travel without difficulty to the mentioned location. Benefits Possibility to organize work shifts according to availability

los paraisos 1010, B2942 Baradero, Provincia de Buenos Aires, Argentina

Negotiable Salary

S&M IAM Marketing Management64520865636993122

Indeed

S&M IAM Marketing Management

Job Vacancies Back S\&M IAM Marketing Management Valentin Alsina, Argentina \| Marketing \| Experienced \| Unlimited \| November 20, 2025 Apply now SHARE As worldwide experts in filtration, MANN\+HUMMEL develop solutions for vehicles, industrial applications, clean air inside vehicles and the sustainable use of water. With team spirit and an open culture of communication, we are continuously working towards achieving our vision of ‘leadership in filtration’. Become part of our team. Job Description Main Tasks* Campaign Planning \& Execution: Designing and managing digital and traditional marketing campaigns to promote filtration products (oil, air, fuel, hydraulic filters). * Social Media \& Content Management: Developing engaging content for social media, blogs, and newsletters, ensuring alignment with brand identity. * Market Research \& Analysis: Conducting studies on industry trends, competitor strategies, and consumer behavior in automotive and industrial sectors. * Budget Management: Oversawing marketing budgets and optimizing media investments for maximum ROI. * Performance Reporting: Preparing KPI reports (ROI, engagement, lead generation) and implementing data\-driven improvements. * Sales Support: Partnered with sales teams to create promotional materials and impactful presentations. * Event Coordination: Organizing company participation in trade shows, exhibitions, and technical training sessions. Your Profile* Education: University degree in Marketing or related fields * Experience: At least 2 years * Language: Fluent English (written and spoken) * Tools: SAP Knowledge * MS Office / Power BI Are you full of ideas? Are you keen to take on responsibility and really achieve something? Then our doors are open to you. This company lives out its values, gives people the freedom to use their own initiative, and offers many development exciting opportunities and many exciting projects – all of which awaits you here.

Belgrano 80, B2938 Alsina, Provincia de Buenos Aires, Argentina

Negotiable Salary

Indeed

waiter/waitress

29/09/2025 ### **waiter/waitress** MARIA NAZARENA ALFONSO Customer service SAN PEDRO, BUENOS AIRES **Offer** ---------- Positions Available 1 Availability Part-time Salary To be determined **Tasks to Perform** --------------------- Job Summary Customer service Main tasks to perform Customer service Benefits Company cafeteria, Health insurance / medical coverage for entire family, Other **Details** ------------ Work Location BUENOS AIRES \- SAN PEDRO \- \- PELEGRINI 900 Availability Part-time Working Days Friday, Saturday, Sunday Start and End Time 17:00 21:00 **Requirements** -------------- Required Experience 2 years Education Level Secondary school Languages * English, minimum knowledge: Basic Computer Skills * Computer, minimum knowledge: Basic Apply Back

Güemes 2040, B2930 San Pedro, Provincia de Buenos Aires, Argentina

Negotiable Salary

Indeed

retail sales assistant

14/10/2025 ### **retail sales assistant** CAMILA FRANGI public customer service SAN PEDRO, BUENOS AIRES **Offer** ---------- Positions Available 1 Availability Part-time Salary To be agreed **Tasks to Perform** --------------------- Job Summary public customer service Main tasks to perform public customer service Benefits Health insurance / medical care for the entire family **Details** ------------ Workplace BUENOS AIRES \- SAN PEDRO \- \- MITRE 1500 Availability Part-time Working Days Monday, Tuesday, Wednesday, Thursday, Friday, Saturday Start and End Time 16:30 20:30 **Requirements** -------------- Required Experience No Education Level Secondary Apply Back

Güemes 2040, B2930 San Pedro, Provincia de Buenos Aires, Argentina

Negotiable Salary

Textile control machine operator or inspector64520852494081125

Indeed

Textile control machine operator or inspector

08/11/2025 ### **Textile control machine operator or inspector** SP INNOVACION SAS SEWING MACHINE OPERATOR IN TEXTILE WORKSHOP SAN PEDRO, BUENOS AIRES **Offer** ---------- Vacancies 1 Work schedule availability Full-time Salary To be determined **Tasks to Perform** --------------------- Job summary SEWING MACHINE OPERATOR IN TEXTILE WORKSHOP Main tasks to perform SEWING MACHINE OPERATOR IN TEXTILE WORKSHOP Benefits Health insurance / medical coverage for the entire family **Details** ------------ Workplace BUENOS AIRES \- SAN PEDRO \- \- CHIVILCOY 2990 Availability Full-time Working days Monday, Tuesday, Wednesday, Thursday, Friday Start and end time 06:00 14:00 **Requirements** -------------- Required experience No Education level Secondary school Apply Back

Güemes 2040, B2930 San Pedro, Provincia de Buenos Aires, Argentina

Negotiable Salary

S&M IAM product manager64384211883651126

Indeed

S&M IAM product manager

Job Vacancies Back S\&M IAM product manager Valentin Alsina, Argentina \| Marketing \| Entry Level \| Unlimited \| November 11, 2025 Apply now SHARE As worldwide experts in filtration, MANN\+HUMMEL develop solutions for vehicles, industrial applications, clean air inside vehicles and the sustainable use of water. With team spirit and an open culture of communication, we are continuously working towards achieving our vision of ‘leadership in filtration’. Become part of our team. Job Description Main Tasks 1\) Leading project management through the incorporation of new products—both locally developed and imported—and the updating of their codes in order to respond efficiently to customer needs. 2\) Updating product catalogs by incorporating or modifying codes and monitoring commercial equivalencies to ensure accurate and timely information for potential customers. 3\) Conducting various types of market research, analyzing variations in demand and the response of the firm and/or competitors to contribute to the company's commercial positioning. 4\) Define pricing strategies based on cost analysis, competition, and perceived value. Monitor margins and ensure competitiveness in the market. 5\) Provide commercial advice, anticipating customer requirements and/or responding to their requests, with the aim of strengthening commercial ties. 6\) Propose improvements and new features based on market insights. Stay up to date on technological and industry trends. 7\) When defining Global Standards, ensure compliance with health, safety, and environmental legislation and take into account the most advanced concepts to ensure healthy, safe, and environmentally friendly production processes, workplaces, and emergency concepts, based on risk assessments. Your Profile* Education: University degree in Engineer Jr. (Industrial, Mechanical, electrical, Electronics) or Bacherlor´s degree in Marketing * Experience: At least 2 years * Language: Fluent English (written and spoken) * Tools: SAP Knowledge * MS Office / Power BI Are you full of ideas? Are you keen to take on responsibility and really achieve something? Then our doors are open to you. This company lives out its values, gives people the freedom to use their own initiative, and offers many development exciting opportunities and many exciting projects – all of which awaits you here.

Belgrano 80, B2938 Alsina, Provincia de Buenos Aires, Argentina

Negotiable Salary

Indeed

Logistics Supervisor

Bunge (www.bunge.com, NYSE: BG) is a global leader in the sourcing, processing, and supply of oilseeds and grain-based products and ingredients. Founded in 1818, Bunge's extensive network provides food and oils to a growing world, creating sustainable products and opportunities for more than 70,000 agricultural producers and consumers of its products worldwide. The company is headquartered in St. Louis, Missouri, and has 25,000 employees globally working across over 350 port terminals, oilseed processing plants, grain storage facilities, and food and ingredient production and packaging sites around the world. The Logistics team at our Ramallo Industrial Unit is seeking a Supervisor who will be responsible for coordinating processes and tasks within their team, aiming to ensure optimal operational conditions, minimizing disruptions, maximizing efficiency, and maintaining industrial safety. **Main responsibilities** * Coordinate and supervise the receipt, storage, and handling of grains and by-products * Supervise truck unloading and ship loading/unloading operations * Supervise dispatch operations for ships and trucks * Manage unloading operations for various products at the port * Monitor the quality of goods being shipped * Ensure quality standards for stored grains and by-products in warehouses * Control proper cleaning of storage warehouses * Record compliance with company safety and quality regulations * Ability to manage multidisciplinary work teams * Monitor and ensure compliance with Industrial Unit safety regulations **Required technical profile** * Graduates with technical degrees in Mechanical, Electrical, Electromechanical or related fields (mandatory) * Minimum of 4 years of experience in industrial roles with leadership responsibilities and personnel under collective agreements (mandatory) * Proven training and/or experience in industrial safety (mandatory) * Knowledge of grain and by-product quality (mandatory) * Proficiency in Microsoft Office Suite * Knowledge of SAP module * Intermediate English proficiency * Availability to work rotating shifts (mandatory) **Work location**: Ramallo Industrial Unit Bunge believes in diversity and recognizes differences as a path to growth. If you are a person with disabilities and are looking for professional opportunities and wish to develop your potential, participate in our selection processes.

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Sales Representative / APM Oncology64309553373571128

Indeed

Sales Representative / APM Oncology

### **Summary** Location: Buenos Aires, Argentina \#Sales Take the next step in your career in a role where your ability to connect, engage, and inspire healthcare professionals can directly impact patients' lives. As a Sales Representative at Novartis, you will be at the forefront of delivering meaningful customer experiences, building trusted relationships, and driving ethical and sustainable sales growth. You'll collaborate with diverse teams, personalize interactions, and transform insights into action, making every conversation count. If you're passionate about health, driven by purpose, and ready to shape the future of medicine, this is your opportunity to make a difference. ### **About the Role** **Key Responsibilities** * Drive competitive sales growth through strategic territory and customer management * Personalize and adapt customer journeys based on healthcare professionals’ preferences and available content * Build long-term, trust-based collaborations with healthcare professionals to support Novartis’ mission * Deliver memorable, customer-centric experiences that go beyond clinical differentiation * Leverage data sources to dynamically create and adjust interaction plans for territories, accounts, and customers * Share customer insights with internal teams to improve content, campaigns, and engagement strategies * Deliver meaningful value to customers and patients in every interaction * Collaborate ethically with cross-functional teams to co-create solutions for unmet needs * Act with integrity and transparency, adhering to the Novartis Code of Ethics and Values * When facing ethical dilemmas, do the right thing and speak up when something seems wrong **Essential Requirements** * Proven sales skills with a track record of meeting or exceeding targets * Ability to understand and act upon customer insights * Excellent verbal and written communication skills * Strong influencing and negotiation abilities * Conflict management skills with a solution-focused approach * Relevant technical competence in the healthcare sector * Experience in account management and cross-functional coordination * High ethical standards and commitment to compliance * **Possession of a valid APM license (mandatory)** **Desirable Requirements** * Experience in the pharmaceutical or healthcare industry Familiarity with digital tools and multichannel sales strategies **Why Novartis:** Helping people affected by disease and their families requires more than innovative science. It takes a community of smart, passionate individuals like you—collaborating, supporting, and inspiring one another—to achieve breakthroughs that transform patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they become available: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division International Business Unit Universal Hierarchy Node Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Sales Job Type Full time Employment Type Regular (Sales) Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Indeed

Tecnico B6º

**How will you CONTRIBUTE and GROW?** ------------------------------------- Tecnico B6º Tecnico B6º **\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_** ------------------------------------------ **Are you a MATCH?** -------------------- Tecnico B6º **Our Differences make our Performance** At Air Liquide, we are committed to build a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world. We welcome and consider applications from all qualified applicants, regardless of their background. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world.

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Indeed

Junior HR Analyst

Based in the Ramallo Industrial Unit, and providing support to the Campana Industrial Unit, our Human Resources team is seeking a Junior Analyst who can utilize the company's tools and methodologies to assist employee needs, aligning with Bunge's corporate strategies. **Main Responsibilities** * Personnel administration: actions related to personnel management, ensuring effective updates of monthly payroll changes and responding to internal clients. * Coordinate the administration of onboarding, offboarding, transfers, and promotions (employee onboarding, induction, communication, entry/exit requisitions, health insurance, etc.). * Organization and updating of personnel documentation (files, insurance, etc.) * Management of procurement processes. * Training and Development: Identify and consolidate training needs. Assist in the dissemination, follow-up, organization, and recording of activities. * Participate in specific diversity initiatives (especially gender balance and inclusion) in talent attraction and internal programs (communications and trainings). * Support the development of Climate Surveys and Action Plans. * Follow-up and update organizational charts and job descriptions across all areas. * Assist the HBRP in labor relations, medical services, and other HR-related tasks. * Recruitment: Collaborate in the administration of the recruitment process. * Support the Industrial Unit in tasks related to Maintenance and improvement of Safety and Hygiene, Environmental, Quality, and Continuous Improvement management systems. **Required Technical Profile** .Graduates with a degree in Human Resources, Labor Relations, or related fields. .Proven experience of at least two years in similar roles within the industrial sector (desirable). .Advanced proficiency in Microsoft Office suite. .SAP knowledge (desirable). .Intermediate level of English. .Availability for occasional travel to the Campana Industrial Unit. We are looking for dynamic candidates with excellent interpersonal skills and the ability to work in a team. **Work Location:** Ramallo Industrial Unit Residence in the area or surrounding regions will be an exclusive requirement. **Internal applications will be accepted until October 3.** Bunge (NYSE: BG) is a world leader in sourcing, processing and supplying oilseed and grain products and ingredients. Founded in 1818, Bunge’s expansive network feeds and fuels a growing world, creating sustainable products and opportunities for more than 70,000 farmers and the consumers they serve across the globe. The company is headquartered in St. Louis, Missouri and has 25,000 employees worldwide who stand behind more than 350 port terminals, oilseed processing plants, grain facilities, and food and ingredient production and packaging facilities around the world. Bunge is an Equal Opportunity Employer. Veterans/Disabled

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Indeed

Finance Specialist

### **Summary** The SSO Finance Specialist is accountable for budget planning, analytics and payment execution in a direct country or extended country group (OPC and satellite countries) in close collaboration with SSO Study Start\-Up Managers, SSO Clinical Project Managers and SSO Contracting Specialists in compliance with Novartis processes, GCP/ICH and regulatory requirements ### **About the Role** **Key responsibilities:** * Supports country SSU strategy in close collaboration with SSO Study Start\-Up Team Lead and SSO Study Start\-Up Managers to ensure SSU timelines and deliverables are met according to country commitments * Responsible for accounting and execution of investigator payments in a direct country or extended study group (OPC and satellite countries) in close collaboration with SSO Study Start\-Up Manager, SSO Clinical Project Manager and SSO Contracting Specialist in assigned projects * Project controlling \& budget management supports financial planning, forecasting and management, analyses and reports project costs and their drivers * Set up \& validation of investigator contracts in the accounting system for clinical studies * Executes and monitors internal controls * Translates Grant Plans into local Payment Schemes **Essential Requirements:** * Bachelor's degree in scientific, finance or economics discipline * Fluent in both written and speaking english and spanish languages. * Financial and business economics background * Independent, dynamic, structured and committed way of working * Communicates effectively in a local/global matrixed environment **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Research \& Development Job Type Full time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Patient Safety Specialist641423797431071212

Indeed

Patient Safety Specialist

### **Summary** Monitors and audits the company's surveillance program for drugs, biologics, or medical devices, including the intake, assessment, processing, and follow-up of adverse reports. Participates in addressing any legal liability and compliance with government regulations. Ensures accurate receipt, maintenance, and evaluation according to product labeling. Reports events or reactions as required by regulatory authorities, including adverse event data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May enable trend and safety signal detection and assessment. Supports all clinical trial activities and post-marketing activities. ### **About the Role** Major Accountabilities \~ Supporting management of operational processes to ensure compliance with Novartis global/local procedures, national and international regulations/standards/guidelines for pharmacovigilance of marketed and investigational products from Novartis \~ Managing the collection, processing, documentation, reporting, and follow-up of all adverse event (AE) reports for all Novartis products from clinical trials, post-marketing studies (PMS), patient support programs (POP), registries, and all spontaneous reports (SR). \~ Accurately and consistently transcribe, translate (if necessary), and enter data from all serious adverse events (from clinical trials) and all adverse events (from POPs, PMS, registries, and all SRs) into safety systems from source documents, emphasizing timeliness and quality. \~ Recording and tracking evidence, submissions, and distribution of documents such as SAEs, SRs, investigator notifications, etc., in collaboration with other departments \~ Managing the reporting/submission/distribution of safety reports/updates/information to local health authorities and/or clinical operations in coordination with other departments. \~ Collaborating with other local/global PV staff to ensure accurate evaluation of safety data. \~ Interacting and exchanging relevant safety information with LHAs, PV staff, other functional groups, and third parties as appropriate. \~ Gathering and monitoring global/regional/national (where applicable) pharmacovigilance regulations and providing updates to the global PVO organization. \~ Developing, updating, and implementing local procedures to ensure compliance with global PVO procedures and national requirements. \~ Managing and maintaining all relevant assigned PVO databases, where applicable. \~ Developing and updating pharmacovigilance training materials \~ Ensuring support and de-escalation of audits, corrective actions and preventive actions (CAPA), and health authority inspections. \~ Providing timely, relevant information to study coordinators, rating agencies, and other Novartis employees \~ Distribution of marketing samples (if applicable) Key Performance Indicators Monitors and audits the company's surveillance program for drugs, biologics, or medical devices, including the intake, assessment, processing, and follow-up of adverse reports. Participates in addressing any legal liability and compliance with government regulations. Ensures accurate receipt, maintenance, and evaluation according to product labeling. Reports events or reactions as required by regulatory authorities, including adverse event data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May enable trend and safety signal detection and assessment. Supports all clinical trial activities and post-marketing activities. Work Experience \~Operations Management and execution \~Cross-border collaboration \~Functional breadth Skills \~Filing (documents) \~Pharmacovigilance \~Safety science insights \~Databases \~Employee training \~Reporting Language English **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Research \& Development Job Type Part time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Pediatric Health Team - Ramallo (Bs.As)641423761272331213

Indeed

Pediatric Health Team - Ramallo (Bs.As)

At Grupo Medihome, we are currently seeking Healthcare Professionals to join our pediatric healthcare team in the Ramallo area, Buenos Aires province. We are looking for graduated and registered professionals in Pediatrics, Physiotherapy, Speech Therapy, and Nursing who reside in or provide patient care within the area. Selected professionals will be responsible for attending to and monitoring pediatric patients requiring home hospitalization, through scheduled visits or on-call shifts, according to professional availability. Requirements **Applicants must have:** Completed Nursing education with corresponding degree Professional license Active monotributo registration or ability to apply for it Benefits Opportunity to organize work schedule according to availability

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Patient Safety Specialist641423679983381214

Indeed

Patient Safety Specialist

### **Summary** Monitor and audit the company's drug, biological product, or medical device surveillance program, including intake, evaluation, processing, and follow-up of adverse event reports. Participate in addressing any legal liability and compliance with government regulations. Ensure accurate receipt, maintenance, and evaluation regarding product labeling. Report required events or reactions to regulatory agencies, including adverse event data from clinical trials, spontaneous or solicited sources, periodic reports, and experience. May provide detection and assessment of safety trends and signals. Support all clinical trial and post-marketing activities. ### **About the Role** Major Accountabilities \~ Support management of operational processes to ensure compliance with Novartis global/local procedures, national and international regulations/standards/guidelines for pharmacovigilance of marketed and investigational Novartis products \~ Manage collection, processing, documentation, reporting, and follow-up of all adverse event (AE) reports for all Novartis products from clinical trials, post-marketing studies (PMS), patient-focused programs (PFP), registries, and all spontaneous reports (SR). \~ Accurately and systematically transcribe, translate (if needed), and enter data from all serious adverse events (from clinical trials) and all adverse events (from PFP, PMS, registries, and all REPORTS) from source documents into safety systems, emphasizing speed and quality. \~ Record and track receipt, submissions, and distribution of documents such as SUSARs, SRs, investigator notifications, etc., in collaboration with other departments \~ Manage reporting/submission/distribution of safety reports/updates/information to local health authorities and/or clinical operations in collaboration with other departments. \~ Work with other local/global PV associates to ensure accurate assessment of safety data. \~ Interact and exchange relevant safety information with LHA, PV associates, other functional groups, and third-party contractors as applicable. \~ Investigate and monitor global/regional/national (as applicable) pharmacovigilance regulations and provide updates to the global PV organization. \~ Develop, update, and implement local procedures to ensure compliance with global procedures and national PV requirements. \~ Management and maintenance of all relevant PV databases as applicable. \~ Develop and update training materials for pharmacovigilance \~ Provide support and closure for audits, corrective action plan activities, and health authority inspections. \~ Provide timely relevant information to trial coordinators, CRAs, and other Novartis employees \~ Distribution of commercial samples (if applicable) Key Performance Indicators Monitor and audit the company's drug, biological product, or medical device surveillance program, including intake, evaluation, processing, and follow-up of adverse event reports. Participate in addressing any legal liability and compliance with government regulations. Ensure accurate receipt, maintenance, and evaluation regarding product labeling. Report required events or reactions to regulatory agencies, including adverse event data from clinical trials, spontaneous or solicited sources, periodic reports, and experience. May provide detection and assessment of safety trends and signals. Support all clinical trial and post-marketing activities. Work Experience \~ Management and execution of operations \~ Cross-border collaboration \~ Functional scope Skills \~ Document submission \~ Pharmacovigilance \~ Safety science \~ Fundamentals \~ Employee training \~ Reporting Language English **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Research \& Development Job Type Part time Employment Type CDI Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Patient Safety Specialist641423677539851215

Indeed

Patient Safety Specialist

### **Summary** Monitors and oversees the company's drug, biological, or medical device safety surveillance program, including intake, evaluation, processing, and follow-up of adverse event reports. Participates in addressing legal liabilities and compliance with government regulations. Ensures accurate receipt, maintenance, and evaluation regarding product labeling. Reports events or reactions as required by regulatory agencies, including adverse event data from clinical studies, spontaneous or solicited sources, periodic reports, and experience reports. May provide signal detection and assessment for safety trends. Supports all clinical trial and post-marketing activities. ### **About the Role** Major Accountabilities \~ Support managing operational processes to ensure compliance with Novartis global/local procedures and national/international regulations, guidelines, and standards for pharmacovigilance of marketed and investigational Novartis products \~ Manage collection, processing, documentation, reporting, and follow-up of all adverse event (AE) reports for all Novartis products from clinical studies, post-marketing studies (PMS), patient-oriented programs (POP), registries, and all spontaneous reports (SR). \~ Accurately and consistently transcribe, translate (where necessary), and enter data from all serious adverse events (from clinical studies) and all adverse events (from POP, PMS, registries, and all SRs) from source documents into safety systems, with emphasis on timeliness and quality. \~ Record and track receipt, submission, and distribution of documents such as SAEs, SRs, investigator notifications, etc., in collaboration with other departments \~ Manage reporting/submission/distribution of safety reports/updates/information to Local Health Authorities and/or clinical operations in coordination with other departments. \~ Collaborate with other local/global PV associates to ensure accurate assessment of safety data. \~ Interact and exchange relevant safety information with LHAs, PV associates, other functional groups, and third-party contractors, as applicable. \~ Identify and monitor global/regional/national (ad hoc) pharmacovigilance regulations and provide updates to the global PVO organization. \~ Develop, update, and implement local procedures to ensure compliance with global PVO procedures and national requirements. \~ Manage and maintain all assigned PVO databases, as applicable. \~ Develop and update pharmacovigilance training materials \~ Ensure support and closure of audits, corrective action plan activities, and health authority inspections. \~ Provide timely and relevant information to study coordinators, CROs, and other Novartis personnel \~ Distribution of marketing samples (if applicable) Key Performance Indicators Monitors and oversees the company's drug, biological, or medical device safety surveillance program, including intake, evaluation, processing, and follow-up of adverse event reports. Participates in addressing legal liabilities and compliance with government regulations. Ensures accurate receipt, maintenance, and evaluation regarding product labeling. Reports events or reactions as required by regulatory agencies, including adverse event data from clinical studies, spontaneous or solicited sources, periodic reports, and experience reports. May provide signal detection and assessment for safety trends. Supports all clinical trial and post-marketing activities. Work Experience \~Operations management and execution \~Cross-functional collaboration \~Functional extension Skills \~Filing (documents) \~Pharmacovigilance \~Safety science \~Databases \~Employee training \~Chronology Language English **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Research \& Development Job Type Part time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Patient Safety Specialist641423496911381216

Indeed

Patient Safety Specialist

### **Summary** Monitors and audits the company's drug safety surveillance program for pharmaceuticals, biological products, or medical devices, including intake, assessment, processing, and follow-up of adverse reports. Participates in addressing any legal liability and compliance with government regulations. Ensures accurate receipt, maintenance, and evaluation consistent with product labeling. Reports events or reactions as required by regulatory agencies, including adverse event data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide detection and evaluation of safety trends and signals. Supports all clinical trial and post-marketing activities. ### **About the Role** Major Accountabilities \~ Support the management of operational processes to ensure compliance with Novartis global/local procedures, national and international regulations/standards/guidelines for pharmacovigilance of marketed and investigational Novartis products \~ Manage the collection, processing, documentation, reporting, and follow-up of all adverse event (AE) reports for all Novartis products from clinical trials, post-marketing studies (PMS), patient-oriented programs (POP), registries, and all spontaneous reports (SR). \~ Transcribe, translate (when necessary), and enter data from all serious adverse events (from clinical trials) and all adverse events (from POPs, PMS, registries, and all SRs) from source documents into safety systems accurately and consistently, emphasizing timeliness and quality. \~ Record and track receipt, dispatch, and distribution of documents such as EFS, SRs, Investigator Notifications, etc., in cooperation with other departments \~ Manage submission/presentation/distribution of safety reports/updates/information to local health authorities and/or clinical operations in cooperation with other Departments. \~ Work with other local/global PV partners to ensure accurate assessment of safety data. \~ Interact and exchange relevant safety information with LHA, PV partners, other functional groups, and external contractors, as appropriate. \~ Survey and monitor global/regional/national pharmacovigilance regulations (as applicable) and provide updates to the global PVO organization. \~ Develop, update, and implement local procedures to ensure compliance with global procedures and national PVO requirements. \~ Manage and maintain all assigned PVO databases, as applicable. \~ Develop and update training materials for pharmacovigilance \~ Ensure support and closure of audits, corrective action plan activities, and Health Authority inspections. \~ Provide timely and relevant information to trial coordinators, CRAs, and other Novartis personnel \~ Distribution of marketing samples (when applicable) Key Performance Indicators Monitors and audits the company's drug safety surveillance program for pharmaceuticals, biological products, or medical devices, including intake, assessment, processing, and follow-up of adverse reports. Participates in addressing any legal liability and compliance with government regulations. Ensures accurate receipt, maintenance, and evaluation consistent with product labeling. Reports events or reactions as required by regulatory agencies, including adverse event data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide detection and evaluation of safety trends and signals. Supports all clinical trial and post-marketing activities. Work Experience \~ Management and execution of operations \~ International collaboration \~ Functional breadth Skills \~ Presentation (Documents) \~ Pharmacovigilance \~ Safety science \~ Foundations \~ Employee training \~ Reporting Language English **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Research \& Development Job Type Part time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Field Execution Analyst641423451534111217

Indeed

Field Execution Analyst

### **Summary** At Novartis Argentina we have \#PassionForTransformingLives. We lead with passion the evolution towards an equitable and sustainable healthcare system, empowering local talent, and refining the formula to support patients in transforming their lives. We do this by focusing on our People, fostering Mastery at work and embracing the Evolution of our model. The Field Execution Analyst will act as the main point of contact for the field force (REPs, MSLs) addressing their requests and providing essential support on CRM platform use. Additionally, this role will ensure data entry integrity, executing strategic decisions to be made based on accurate data, and will support the business by fulfilling different data needs of field execution and respective KPIs. ### **About the Role** **Major Accountabilities:** * Administrate and update the CRM platform, participating in the implementation of new functionalities. * Propose and implement data cleaning activities, ensuring the integrity of the database. Working close with Data Architecture team. * Generate and analyze CRM information reports and present data \& insights to FLMs and brand teams. * Implement and follow up tracking KPIs that facilitate data\-driven decision\-making. * Resolve requests related to the use and management of the CRM. Manage field force request or platform issues, ensuring timely resolutions. * Administrate the logistics of free of charge products delivery process. Ensuring excellence in customer experience. * Collaborate with different areas to ensure the correct implementation and use of the CRM and participate in strategic projects in the Business Excellence \& Execution area. * Reporting technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt **Technical Skills and specifications:** * Completed or ongoing (advanced) university studies, preferably in engineering, economic sciences or related fields (mandatory). * Knowledge of CRM platforms (Salesforce desirable) * Knowledge of Microsoft Automate, MS Lists, Copilot and RPA tools (e.g., SharePoint, Power Automate) is desirable * High proficiency in MS Office, Excel and PowerPoint (mandatory) * Intermediate/Advanced oral and written English (mandatory). * Data visualization tools (Desirable Power BI) **Other desired Competencies:** * Proactive person, resolute with critical thinking. * Deadline\-oriented with prioritization abilities. * Effective team player with strong collaboration skills and the ability to work with different roles within the organization. * Analytical profile with attention to detail and independent working skills. * Ability to handle multiple tasks simultaneously **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division International Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Marketing Job Type Full time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Welded Innovation & Improvement Trainee - SIAT VA641423381218591218

Indeed

Welded Innovation & Improvement Trainee - SIAT VA

At **Grupo Techint**, we offer you a professional growth environment, with a training plan tailored to your needs and the opportunity to build your career every day. You will be able to work within teams that pursue excellence and are always looking to learn together, contributing knowledge and innovation to every project. If you are currently studying **Computer Science and/or Systems** and have more than 50% of your degree completed, we have a vacancy for you as a **Welded Innovation & Improvement Trainee - SIAT VA** to work at the **Valentín Alsina plant**. Main responsibilities: * Analyze large volumes of data from the production line using Python and SQL. * Identify relationships between process variables and their impact on product quality or operational efficiency through the use of artificial intelligence tools. * Propose and evaluate modifications to machine setup parameters to optimize performance indicators. Requirements: * Students pursuing a degree in **Computer Science and/or Systems**, with at least 50% of the program completed, including final exams. * Intermediate English proficiency. * Programming knowledge. *Tenaris offers you the chance to create something new and incredible every day.* ***We invite you to discover it—apply now!***

Belgrano 80, B2938 Alsina, Provincia de Buenos Aires, Argentina

Negotiable Salary

Patient Safety Specialist640556180409631219

Indeed

Patient Safety Specialist

### **Summary** * Monitors and audits the company’s drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow\-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. Ensures accurate receipt, maintenance and assessment against product labeling. Reports events or reactions as required by regulatory agencies including adverse events data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide trending and safety signal detection and assessment. Supports all clinical trial activity and post marketing. ### **About the Role** **Major accountabilities:** * To support management of operational processes in ensuring compliance with Novartis global/local procedures, national and international regulations/standards/guidelines for pharmacovigilance of Novartis marketed and investigational products \-Manage collection, processing, documentation, reporting and follow\-up of all adverse events (AE) reports for all Novartis products from clinical trials, post\-marketing studies (PMS), Patient Oriented Programs (POP), registries and all Spontaneous Reports (SR). * Transcribe, translate (where required) and enter data of all Serious Adverse Events (from Clinical Trials,) and all adverse events (from POPs, PMS, registries and all SRs) from source documents onto safety systems accurately and consistently with emphasis on timeliness and quality. * Record and track receipts, submissions and distributions of documents like SAEs, SRs, Investigator Notifications etc in cooperation with other departments \-Manage reporting/submission/distribution of safety reports/updates/information to Local Health Authorities and/or clinical operations in cooperation with other Departments. * Work with other local/global PV associates to ensure accurate evaluation of safety data. * Interact and exchange relevant safety information with LHA, PV associates, other functional groups and third party contractor, if applicable. * Survey and monitor global/ regional/national (as applicable) pharmacovigilance regulations and provide update to global PVO organization. * Develop, update and implement local procedures to ensure compliance with PVO global procedures and national requirements. * Management and maintenance all relevant assigned PVO databases, if applicable. * Develop and update training materials for pharmacovigilance \-Ensure support for and close\-out of audits, corrective action plan activities and Health Authority inspections. * Provide timely, relevant information to trial coordinators, CRAs and other Novartis staff \-Distribution of marketing samples (where applicable) **Key performance indicators:** * Adherence to Novartis policy and guidelines \-Project and stakeholder feedback \-Operational risk mitigation and audit/inspection findings \-Quality and timely reporting of KPI and safety reports/updates \-Results of audits/inspections **Minimum Requirements:** * Bachelor's Degree * Fluent English \& Spanish * Experience with databases/dashboards **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Research \& Development Job Type Part time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Production - Manufacturing Engineering638368180194591220

Indeed

Production - Manufacturing Engineering

Production \- Manufacturing Engineering Valentin Alsina, Argentinien \| Produktion \| Berufserfahrene \| Unbefristet \| May 15, 2025 As worldwide experts in filtration, MANN\+HUMMEL develop solutions for vehicles, industrial applications, clean air inside vehicles and the sustainable use of water. With team spirit and an open culture of communication, we are continuously working towards achieving our vision of ‘leadership in filtration’. Become part of our team. Job Description Role Summary The incumbent oversees the development and implementation of manufacturing processes, maintenance processes and tool shop processes (if applicable). A team of advanced manufacturing engineers, project engineers, production engineers, maintenance engineers and tooling engineers are supporting the fulfillment of tasks. Main Tasks* Establish and maintain exchange with global manufacturing engineering * Apply latest technology from related industry to ensure competitiveness * Ensure the appropriate balance between automation and manual production processes * Manage preventive and predictive maintenance through analysis, planning, and monitoring of periodic and occasional inspections to ensure the uninterrupted operation of factory equipment. * Manage the repair, modification, and/or development of machinery through collaboration with specialized suppliers to ensure that the equipment is suited to the plant's needs. * Ensure with Operation and Supply Chain Management required access to plant equipment for new product introduction (tuning, pre\-series and training phases) and maintenance activities * Ensure compliance with HSE legislation; apply policies and processes; provide healthy, safe and environmentally friendly work places and state\-of\-the\-art production processes and infrastructure; * Ensure that all relevant internal and external norms and standards (e.g. ISO/IATF) are applied * \#LI\-Onsite Your Profile We offer Are you full of ideas? Are you keen to take on responsibility and really achieve something? Then our doors are open to you. This company lives out its values, gives people the freedom to use their own initiative, and offers many development exciting opportunities and many exciting projects – all of which awaits you here.

Belgrano 80, B2938 Alsina, Provincia de Buenos Aires, Argentina

Negotiable Salary

Electromechanical Maintenance Supervisor638367984787211221

Indeed

Electromechanical Maintenance Supervisor

Do you have experience in Electromechanical Maintenance? **Main responsibilities will be:** Coordinate the tasks of the corrective, preventive, and predictive maintenance program carried out in SAP systems for machinery and equipment under your responsibility. Ensure in the field that electromechanical maintenance tasks comply with necessary safety requirements (work permits, lockouts, etc.). Work to improve troubleshooting times by identifying training needs, resources, or other needs within the team under your supervision. Monitor overtime hours, leaves, and all management related to the roles under your responsibility. Provide technical support to planners for preparing tasks to be executed. Analyze results and propose necessary improvements. Collaborate with the planning team to enhance maintenance programs and critical spare parts lists. Marfrig's operation in Argentina is a leader in the production and sale of bovine meat-derived and processed foods in the country. It has 4 plants with a capacity of over 39 thousand tons of hamburgers per year and more than 30 thousand tons of other products annually, including processed foods such as franchises and cold cuts. La Morocha, Quickfood, Good Beef, and Gaucho Beef are brands representing some of the highest quality beef in the world. Marfrig in Argentina stands out for its leading brands, not only in meats but also in processed products such as Paty, a brand synonymous with hamburgers, and Vienissima!, a sausage brand. The company is recognized for its integrity, excellence, and commitment to sustainability, as well as a productive model that respects legal, environmental, and animal welfare aspects. Requirements You are an advanced student in Engineering and/or an Electromechanical, Mechanical, or Electrical Technician. At least three years of experience in the field within process industries. **Work Location:** Baradero.

los paraisos 1010, B2942 Baradero, Provincia de Buenos Aires, Argentina

Negotiable Salary

Indeed

Quality Supervisor

At MBRF we are looking for a Quality Control Supervisor **Your main responsibilities will be:** Execute the control program at the plant. Lead the plant's team of analysts. Participate in the plant's HACCP team and QMS processes. Monitor sensory results, participate in complaint handling, follow up on action plans, and prepare route sheets together with the plant technician. Marfrig's operation in Argentina is a leader in the production and sale of bovine meat-derived and processed foods in the country. There are 4 plants with a capacity of more than 39 thousand tons of hamburgers per year and over 30 thousand tons of other products annually, including processed foods such as franchises and cold cuts. La Morocha, Quickfood, Good Beef, and Gaucho Beef are brands representing some of the finest quality beef in the world. Marfrig in Argentina stands out for its leading brands, not only in meats but also in processed products such as Paty, a brand synonymous with hamburgers, and Vienissima!, for sausages. The company is recognized for its integrity, excellence, and commitment to sustainability, and for a productive model that respects legal, environmental, and animal welfare aspects. Requirements We are seeking advanced students or graduates in Biochemistry, Food Engineering, or related fields. Experience in the food or meatpacking industry (2-3 years) will be valued. Knowledge of food safety and regulations is required for this position. Full-time availability. Willingness to relocate. The company provides benefits related to relocation support. **Work location:** Baradero.

los paraisos 1010, B2942 Baradero, Provincia de Buenos Aires, Argentina

Negotiable Salary

Occupational Health and Safety Analyst638367942451211223

Indeed

Occupational Health and Safety Analyst

At MBRF, we are seeking to hire a Technical Analyst in Occupational Health and Safety. **Main responsibilities will include:** Comply with various tools of the management system for the prevention of accidents and occupational diseases. Compliance with applicable current legislation in the field. Participate in campaigns and events organized by the department. Participate in investigations of various incidents (workplace accidents, occupational diseases, commuting accidents, process accidents, environmental accidents, deviations, etc.). Identify risks, unsafe conditions, and unsafe acts. Compliance with the execution and participation in DSST activities. Participate in various assigned committees (Unit HSE Committee and Joint Committee). Comply with the annual training plan assigned. Manage third parties (contractor companies). Enforce and ensure compliance with the company's general safety rules. Serve as a member of the emergency brigade and support the unit's emergency and contingency response plan. Marfrig's operations in Argentina are leaders in the production and sale of beef-derived and processed food products in the country. It operates four plants with an annual capacity of over 39 thousand tons of hamburgers and more than 30 thousand tons of other products, including processed foods such as franchises and cold cuts. La Morocha, Quickfood, Good Beef, and Gaucho Beef are brands representing some of the finest quality beef in the world. Marfrig in Argentina stands out for its leading brands, not only in meat but also in processed products such as Paty, a brand synonymous with hamburgers, and Vienissima!, a sausage brand. The company is recognized for its integrity, excellence, and commitment to sustainability, as well as a production model that respects legal, environmental, and animal welfare standards. Requirements Graduate of Technical Program in Occupational Health and Safety Minimum two years of experience in food production plants (desirable) **Work location:** Baradero.

los paraisos 1010, B2942 Baradero, Provincia de Buenos Aires, Argentina

Negotiable Salary

Maintenance Supervisor Valentín Alsina Argentina638367906048011224

Indeed

Maintenance Supervisor Valentín Alsina Argentina

**Tenaris** is a leading company in the production of tubes and provider of services for the energy industry. Our mission is to deliver value to our customers through product development, manufacturing excellence, and supply chain management. We are looking for a **Maintenance Supervisor** to join directly the work team. The Maintenance Supervisor is responsible for the installation and stabilization of production machinery, diagnosing and repairing equipment failures, working with hydraulic and pneumatic systems, reading and interpreting diagrams and blueprints, scheduling preventive maintenance for all equipment, performing systematic analysis of problems and improvement opportunities. **Main responsibilities:** * Supervision and organization of plant personnel (shift assignment, absenteeism control, etc) * Task distribution and management of the team in charge * Ensure required quality standards * Ensure compliance with safety regulations * Meet assigned performance indicators * Report to the operations and maintenance manager * Analyze results and propose necessary improvements * Maintenance scheduling **Candidates with experience in similar roles within industrial companies will be valued** **Requirements:** * Availability to work rotating shifts (morning, afternoon and night, Monday to Monday with rotating day off). * Experience in similar positions within industrial companies * Experience in indicator analysis * Reside in nearby areas * Conflict resolution skills If you are interested in this position, upload your CV and apply. Check our privacy policy at the following link.

Belgrano 80, B2938 Alsina, Provincia de Buenos Aires, Argentina

Negotiable Salary

Facilities Coordinator - Argentina638367783642891225

Indeed

Facilities Coordinator - Argentina

### **Summary** We are looking for a Facility Manager to lead site operations, vendor management, and workplace services with a strong focus on compliance and customer satisfaction. The role includes overseeing maintenance, GxP environments, and service contracts, while driving sustainability and efficiency. Candidates should have technical expertise in facility management, leadership skills, and experience in regulated industries. A degree in Business, Architecture, or Engineering is required. ### **About the Role** \#LI\-Hybrid Location: Argentina **Key Responsibilities:** ------------------------- * **Facility Operations \& Customer Engagement** Ensure the workplace is comfortable and productive for employees. Collect and act on customer feedback to improve workplace satisfaction. Manage space allocations, office moves, and seating arrangements according to business needs. Address daily facility issues, ensuring reliable and efficient site operations. * **Maintenance \& Compliance** Oversee preventive maintenance to ensure buildings and facilities are functional, safe, and compliant with regulations. Monitor health, safety, and energy usage to improve efficiency and sustainability. Assurance GxP compliance on Quality Control and Microbiology Labs environment under facility management scope * **Vendor and Service Management** Work with procurement to ensure cost\-effective services. Manage providers for cleaning, security, landscaping, food services, etc., and assess their performance using metrics like SLAs and KPIs. Overseed providers for Laboratory services under Facility scope (Including GxP services) Support /Negotiate contracts and identify opportunities for cost reduction. Support Expenses forecast estimation for services providers. * **Workplace Support Services** Supervise non\-technical services such as reception, mail delivery, cleaning, pantry management, office supplies, and transportation. Coordinate services like parking, shuttle management, and other operations. * **Health, Safety, and Environment Compliance** Ensure facilities meet health, safety, and environmental standards. Promote a positive safety culture and proactively mitigate risks. Ensure 3rd party services providers follow HSE and GxP requirements when they apply. Support local government inspections and remediation plans in case of any finding. * **Real Estate Management** Communicate with landlords on building maintenance and sustainability improvements. Handle/support lease\-related negotiations with Procurement and Legal. Collaborate on service delivery and improvements. * **Metrics and Reporting** Track and report key performance indicators (KPIs) such as financial results, customer satisfaction, and energy efficiency. Provide insights into space usage, service quality, and cost efficiencies. * **Project Responsibilities** Support office relocations, fit\-outs, and small\-scale construction projects (typically \< $100,000\).Coordinate with vendors, prepare scopes of work, and ensure timely, budget\-conscious delivery. Document project progress and completion supporting activities for Project Management. Lead initiatives to improve sustainability, energy efficiency, and employee satisfaction. Build relationships with customers, vendors, and internal teams. Manage sub\-tenant interactions and resolve facilities\-related requests. Develop workflows and address operational challenges with innovative solutions. **Main Requirements:** ---------------------- * Bachelor’s degree in Business Administration, Architecture, or Engineering (Engineering preferred for technical sites) * 3\-5 years of proven experience in facility management within regulated industries * At least 2 years in current role as Facility Manager. * Strong knowledge of GxP environments and compliance standards * Demonstrated ability to lead cross\-functional projects and vendor teams * Skilled in vendor selection, contract negotiation, and performance evaluation * Proactive problem\-solver with a focus on business continuity and operational excellence * Excellent communication and interpersonal skills for stakeholder engagement * Experience managing preventive maintenance and sustainability initiatives * Familiarity with health, safety, and environmental (HSE) regulations * Ability to manage budgets, forecasts, and cost\-efficiency metrics * English and Spanish proficiency required **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Operations Business Unit CTS Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Alternative Location 1 Olivos, Argentina Functional Area Facilities \& Administration Job Type Full time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Portfolio Commercial Lead638349089932811226

Indeed

Portfolio Commercial Lead

### **Summary** LI\-Hybrid Location: Buenos Aires, Argentina Relocation Support: This role is based in Buenos Aires, Argentina. Novartis is unable to offer relocation support: please only apply if accessible. Are you ready to drive innovation and shape the future of healthcare in Argentina? As the Portfolio Commercial Lead at Novartis, you’ll play a pivotal role in transforming patient outcomes and advancing our mission to deliver equitable, sustainable healthcare. You’ll lead strategic initiatives, empower local talent, and champion digital\-first solutions that set new standards in the industry. Join us to make a meaningful impact—where your expertise and vision will help redefine what’s possible for patients, teams, and the broader healthcare ecosystem. ### **About the Role** **Key Responsibilities** ------------------------ * Develop and execute innovative marketing strategies aligned with Novartis’ vision and portfolio goals. * Lead market analysis to identify trends, stakeholder needs, and unlock new business opportunities. * Launch new commercial models using integrated, digital\-first, and differentiated go\-to\-market approaches. * Drive impactful omnichannel engagements and field activation through real\-time data and digital platforms. * Foster cross\-functional collaboration, ensuring alignment with global and regional strategies for seamless execution. **Essential Requirements** -------------------------- * Bachelor’s degree in Pharmacy, Life Sciences, Commercial, Marketing, or Communication. * Minimum 5 years of experience in the pharmaceutical industry in marketing, sales, or commercial roles. * Strong understanding of the healthcare system and regulatory environment. * Proven leadership and project management experience. * High proficiency in digital tools, data analytics, and generative AI. * Fluent in both Spanish and English. **Desirable Requirements** -------------------------- * MBA degree preferred. **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division International Business Unit Universal Hierarchy Node Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Marketing Job Type Full time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary

Sr Sales Administration Analyst638348863557151227

Indeed

Sr Sales Administration Analyst

### **Summary** At Novartis Argentina we lead with passion the evolution towards an equitable and sustainable healthcare system, empowering local talent, and refining the formula to support patients in transforming their lives. We do this by focusing on People, fostering Mastery at work, and embracing the Evolution of our model. Handling transactions related to the Social Security and HMO Health Maintenance Organization system, applied to the Oncology and Special Treatments product segment. Analysis and dispatch of stock, settlements, invoicing, reports and sales analysis. ### **About the Role** **Key Responsibilities:** * Provide analytical support to managers on matters related to FSC activities, decision\-making and general projects. * Assist more senior colleagues by providing analysis contributing to financial, reporting and accounting processes. * Contribute to the preparation of analysis and reports with particular emphasis on the accuracy, compliance and timeliness of the data provided (i.e., reports on profit and loss activity). * Support the preparation of reports on relevant facts and figures for internal and external reports, in a timely and accurate manner. * Assist in the preparation of written project proposals, analytical reports and presentations. * Contribute to the maintenance of accurate and timely information on fixed assets in the fixed assets register and provide support in the General Ledger, as needed. * Provide assistance in Finance Projects in the country or in the BU. * Notification of technical complaints/adverse events/special case scenarios related to Novartis product * Distribution of marketing samples (where applicable). **Main requirements:** * Bachelor's degree in Business Administration or International Trade or similar. * \+2 years experience in the healthcare sector * Proven experience with data analysis and report generation * Knowledge of distribution channels in a pharmaceutical company: public tenders, agreements, private sector * Excel proficiency (intermediate/advanced) * Handling urgent requests / delivery follow\-up * English proficiency **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division International Business Unit Universal Hierarchy Node Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Audit \& Finance Job Type Full time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Negotiable Salary