Accounts Payable Analyst Temporary Position At Abbvie Heredia jobs in Heredia – Browse 77 openings on RoboApply Jobs
Accounts Payable Analyst Temporary Position At Abbvie Heredia jobs in Heredia
Open roles matching “Accounts Payable Analyst Temporary Position At Abbvie Heredia” with location signals for Heredia. 77 active listings on RoboApply Jobs.
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Accounts Payable Analyst - Temporary Position at AbbVie | Heredia
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Experience Level
Entry Level
About the job
AbbVie is seeking an Accounts Payable Analyst for an 11-month temporary assignment based in Heredia. This role centers on handling invoice processing and supporting the company’s financial operations.
What you will do
Process and manage invoices in line with company policies and procedures
Maintain accurate and organized financial records
Support compliance efforts within the accounts payable function
Who this role suits
This position is well-suited for entry-level candidates interested in developing skills in finance and accounting. The temporary nature of the role provides practical experience in a corporate setting.
Location and duration
Based in Heredia, this assignment is set for 11 months.
AbbVie is seeking an Accounts Payable Analyst for an 11-month temporary assignment based in Heredia. This role centers on handling invoice processing and supporting the company’s financial operations. What you will do Process and manage invoices in line with company policies and procedures Maintain accurate and organized financial records Support compliance …
Purpose StatementAs a Quality Engineer, your primary role will be to ensure that our products are both functional and safe for end users. You will achieve this by understanding, developing, and applying quality control systems, while also analyzing, proposing, and implementing enhancements to quality and manufacturing processes. Your focus will be on timely and efficient defect resolution.Major Responsibilities• Assess, recommend, and implement medium complexity process improvements within the quality area, aiming to enhance efficiency while being guided by the area manager.• Identify solutions to challenges in manufacturing and process quality through Lean methodologies.• Assist in root cause investigations (NCRs) and contribute to the development and execution of action plans within specified timelines. Review and approve documents for Medium Impact NCR.• Evaluate and approve quality plans and First Article Plans related to production processes of low to medium complexity, suggesting modifications to PFMEAs for assigned projects.• Conduct reviews of OT Core System documents and validation/qualification protocols (IQ, PPQ, IOQ, IO, PR, etc.) where designated as a quality representative in complex systems.• Support key company initiatives, including the establishment and execution of controls to guarantee product quality.• Maintain orderliness and cleanliness in responsible areas (5's) and adhere to quality goals within the designated timeframe.• Execute additional functions relevant to the position and those assigned by your direct manager.• Ensure compliance with corporate and legal EHS requirements by adhering to internal policies and procedures, while promoting compliance through strategic planning, internal controls, communication, and training.• Actively engage in maintaining EHS results through leadership, commitment, and participation in all EHS-related initiatives.
Job Objective: Oversee and coordinate all production activities within the manufacturing facility, ensuring that teams and resources are managed effectively to meet key goals surrounding efficiency, quality, safety, and output. Cultivate an optimal work environment while driving continuous process improvements.Main Responsibilities:Lead production teams by overseeing scheduling, training, motivation, and performance management of line staff.Ensure that operations are efficient and organized, adhering to all relevant procedures, standards, and regulations (GMP, FDA, ISO, OHSAS, SOX, etc.).Analyze and implement continuous improvement strategies aimed at reducing defects and scrap while enhancing yields and productivity through lean manufacturing, Six Sigma, and advanced problem-solving techniques.Ensure product traceability and quality through thorough reviews of units, routers, and labels, alongside meticulous record-keeping in manufacturing systems (SFA, SAP, Kronos, or equivalent).Manage and track key performance indicators and production metrics, preparing regular reports to communicate progress, incidents, and outcomes.Facilitate smooth shift transitions to maintain operational continuity and uphold production plans.Participate in audits, investigate non-conformities, and ensure adherence to corporate and legal EHS requirements, including relevant tasks and training.Develop and execute corrective and preventive measures related to safety, quality, efficiency, and team collaboration culture.Work closely with support departments (Engineering, Quality, Materials, HR) to set priorities, allocate resources, and execute projects.Promote a safe, positive work atmosphere that emphasizes team development, inclusion, and diversity.
General Purpose: Lead, mentor, and oversee dynamic customer service teams engaged in policy servicing operations, access and reimbursement, and global complaint management. Drive operational excellence and ensure compliance with regulations while cultivating high standards of customer, patient, and consumer satisfaction. Collaborate across departments to implement strategies that elevate the customer experience, enhance operational efficiency, and foster business growth in both local and global highly regulated environments.Key Responsibilities:Guide and develop cross-functional teams in customer service, operations, access/reimbursement, and complaint management, nurturing a culture of high performance and continuous improvement.Oversee customer support, policy servicing, call/contact centers, and complaint resolution operations, ensuring adherence to SLA, KPIs, and regulatory/global standards.Design and implement strategies to enhance customer/user experiences, initiate continuous improvement projects, and integrate technological solutions to optimize processes and outcomes.Manage data handling, performance metrics analysis, reporting, and compliance/audit processes efficiently.Create and execute operational business plans, access/reimbursement strategies, and comprehensive training programs for both internal and external teams.Maintain strong stakeholder relationships, including commercial teams, vendors, technical areas, strategic partners, and regulators across multiple countries.Ensure thorough documentation, investigation, and reporting of complaints/adverse events, and maintain communication with internal/external customers, including drafting regulatory-compliant formal responses.Encourage innovation, digital tool adoption, automation, and transformation initiatives that align with business needs and industry trends.Support and educate teams, clients, and customers on administrative, technical, and regulatory processes.Champion initiatives promoting inclusion, diversity, well-being, and talent development within the organization.
General Purpose: As a Quality Complaint Specialist, you will play a crucial role in supporting and conducting thorough investigations into complaints related to medical and pharmaceutical products. You will manage, document, and report quality events while ensuring compliance with regulatory standards, promoting continuous improvement, and achieving service excellence. This role requires collaboration with both internal and external teams, fostering a culture of inclusivity.Main Responsibilities:Investigate, analyze, and follow up on product complaints, performing functional, visual, or dimensional testing as necessary.Document all pertinent information including product history, device records, risk documentation, and labeling, while adhering to good laboratory, manufacturing, and documentation practices.Identify the root causes of complaints and perform basic statistical analysis, reporting findings to relevant teams.Recognize potentially reportable events and escalate them appropriately to the PMS Manager, Clinical Specialist, or regulatory authorities.Assist in managing Corrective and Preventive Actions (CAPAs), Non-Conformance Event Procedures (NCEPs), Out of Trend (OOT) investigations, and other compliance and improvement initiatives.Engage in continuous improvement and innovative projects related to complaint investigation processes.Utilize documentation systems (QMS, databases, tracking sheets) to monitor, track, and report outcomes efficiently.Train colleagues in processes and products as needed.Facilitate product integration and transfers between different sites.Support environmental health and safety (EHS) initiatives, ensuring proper calibration, preventive maintenance, and control of laboratory equipment.Ensure timely and effective closure of complaint investigations.Assist in communications with third parties including OEMs, Contract Manufacturers, internal clients, and various functional areas.
Join AbbVie, a global biopharmaceutical company committed to discovering and delivering innovative medicines that solve serious health issues. We are currently seeking dedicated Production Operators for a temporary contract of 6 months. The available shifts include both morning and afternoon schedules.
 As a Supplier Quality Engineer III at AbbVie, you will play a vital role in collaborating with suppliers to ensure that all materials and services meet stringent quality specifications and comply with company standards. You will maintain the integrity of our approved suppliers by documenting processes necessary to satisfy regulatory agency requirements and the QMR03 Supplier Controls policy. This position requires close coordination with various departments to achieve established goals and adhere to established procedures.Key Responsibilities:• Manage the initiation, notification, tracking, and closure of Supply Corrective Action Requests (SCARs) as the Quality Contact in the GTW system.• Monitor materials that are blocked, on hold, or quarantined to facilitate compliant material disposition aligned with business objectives. Review and approve the disposition of non-conforming materials.• Participate in the Center of Excellence (CoE) meetings focusing on supplier metrics and controls, escalating any pertinent issues, changes in corporate procedures, or CoE-managed projects to management.• Assist in executing assigned project-related activities, including supply assurance, product introductions, supplier qualifications, and supply change notifications.• Process change notifications from local and international suppliers, collaborating with the Global GSQM department and forming interdisciplinary teams to evaluate impacts across company departments.• Prepare, coordinate, and execute First Articles and Change Plans related to the evaluation of materials affected by change notifications or new qualifications.• Ensure that specifications for new material qualifications or changes are adequate for incoming materials.Additional responsibilities may include addressing deviations, non-conformance reports, corrective and preventive actions, and participating in cross-functional team meetings and internal audits.
Role Overview Experian is seeking a Business Analyst in Heredia. This position focuses on analyzing business processes and finding ways to improve them. The Business Analyst provides insights that support strategic decision-making across the company. What You Will Do Review and analyze existing business processes Identify areas where improvements can be made Deliver clear, actionable insights to support strategy Work closely with teams across different departments Help ensure solutions align with client and stakeholder needs Collaboration This role involves frequent interaction with cross-functional teams to make sure business solutions are effective and relevant.
Join Experian, a global leader in data analytics and information services, as a Senior Business Analyst. In this role, you will utilize your analytical skills to identify business needs, develop strategies, and improve operational efficiencies. You will work closely with stakeholders to gather requirements, conduct data analysis, and deliver actionable insights that drive decision-making.
Join Experian as a Senior Accounting Analyst – Revenue, where you will play a vital role in managing and analyzing revenue streams. This position demands a keen analytical mind and deep understanding of accounting principles to provide insights that drive our financial strategies.
Join AbbVie, a global biopharmaceutical company, as a Manufacturing Supervisor. In this role, you will lead a dynamic team in the production of life-changing medicines. Your expertise will guide the team in achieving operational excellence while adhering to safety and quality standards.
Join AbbVie, a global leader in biopharmaceuticals, as a Quality Engineer. In this role, you will be responsible for ensuring the highest quality standards are maintained throughout our manufacturing processes. You will collaborate with cross-functional teams to implement quality assurance strategies, conduct audits, and support compliance initiatives.
Join AbbVie as a Complaint Resolution Specialist I in our Heredia office. In this entry-level position, you will play a vital role in ensuring customer satisfaction through effective resolution of complaints. You will be responsible for responding to customer inquiries, investigating complaints, and providing timely feedback, ensuring that our clients receive the highest level of service.
Join AbbVie as a Manufacturing Engineer, where you will play a pivotal role in our production processes. We are seeking a motivated engineer with a passion for optimizing manufacturing operations and enhancing product quality. In this role, you will be responsible for the analysis and improvement of manufacturing procedures, ensuring compliance with industry standards, and collaborating with cross-functional teams to drive innovations.
Join Experian as an iOS Developer and be part of a dynamic team that is revolutionizing the way consumers interact with their financial data. In this role, you will design and implement cutting-edge mobile applications that enhance user experience and drive customer engagement.
Join AbbVie as a Complaint Processing Supervisor in Heredia, where you will play a pivotal role in ensuring customer satisfaction by efficiently managing and resolving complaints. This entry-level position offers a unique opportunity to grow within a leading biopharmaceutical company dedicated to improving patients' lives.
Join AbbVie as a Quality Complaints Specialist, where you will play a vital role in ensuring the highest quality of our products through thorough investigation and resolution of quality complaints. You will collaborate with cross-functional teams to analyze data, identify trends, and implement corrective actions to enhance quality assurance processes.
Experian is looking for a Senior Data Engineer to join the team in Heredia. This role focuses on designing, building, and maintaining scalable systems that support data-driven decision-making across the company. Role overview The Senior Data Engineer will work closely with colleagues from different departments to understand business needs and turn them into effective data solutions. The position involves shaping data architecture, developing and optimizing ETL processes, and supporting cloud-based infrastructure. What you will do Design and maintain scalable data processing systems Enhance and support data infrastructure using cloud technologies Collaborate with cross-functional teams to gather and translate requirements Optimize data workflows for quality and reliability Requirements Experience in data architecture and ETL processes Strong background in cloud technologies Analytical skills to improve data quality and workflows Ability to work effectively with teams across the business
The Senior Manager of Post-Market Complaint Operations at AbbVie oversees a team responsible for handling product complaints and supporting ongoing product quality. This position is based in Heredia and focuses on upholding safety standards and regulatory compliance after products reach the market. Role overview This leader guides the complaint operations team, ensuring that processes align with internal standards and external regulations. The role involves direct coordination with regulatory agencies and helps define strategies for post-market surveillance. Attention to detail and a commitment to patient safety are central to this work. Key responsibilities Lead and develop the team managing post-market complaint operations Drive compliance with regulatory requirements and company policies Oversee effective communication with regulatory bodies Shape strategies for monitoring product performance and safety after launch Impact This position plays a crucial role in maintaining AbbVie's standards for product safety and quality, directly supporting the company’s commitment to patients and regulatory partners.
Role Overview Experian is looking for a Senior Data Engineer with AWS expertise to join the team in Heredia. This role focuses on designing, building, and maintaining data pipelines that support analytics and operations. The position plays a key part in enabling data-driven decision-making across the company. What You Will Do Design and develop data pipelines on AWS Maintain and optimize existing data infrastructure Work closely with analytics and operational teams to deliver reliable data solutions Collaborate with colleagues from different departments to improve data processes
AbbVie is seeking an Accounts Payable Analyst for an 11-month temporary assignment based in Heredia. This role centers on handling invoice processing and supporting the company’s financial operations. What you will do Process and manage invoices in line with company policies and procedures Maintain accurate and organized financial records Support compliance …
Purpose StatementAs a Quality Engineer, your primary role will be to ensure that our products are both functional and safe for end users. You will achieve this by understanding, developing, and applying quality control systems, while also analyzing, proposing, and implementing enhancements to quality and manufacturing processes. Your focus will be on timely and efficient defect resolution.Major Responsibilities• Assess, recommend, and implement medium complexity process improvements within the quality area, aiming to enhance efficiency while being guided by the area manager.• Identify solutions to challenges in manufacturing and process quality through Lean methodologies.• Assist in root cause investigations (NCRs) and contribute to the development and execution of action plans within specified timelines. Review and approve documents for Medium Impact NCR.• Evaluate and approve quality plans and First Article Plans related to production processes of low to medium complexity, suggesting modifications to PFMEAs for assigned projects.• Conduct reviews of OT Core System documents and validation/qualification protocols (IQ, PPQ, IOQ, IO, PR, etc.) where designated as a quality representative in complex systems.• Support key company initiatives, including the establishment and execution of controls to guarantee product quality.• Maintain orderliness and cleanliness in responsible areas (5's) and adhere to quality goals within the designated timeframe.• Execute additional functions relevant to the position and those assigned by your direct manager.• Ensure compliance with corporate and legal EHS requirements by adhering to internal policies and procedures, while promoting compliance through strategic planning, internal controls, communication, and training.• Actively engage in maintaining EHS results through leadership, commitment, and participation in all EHS-related initiatives.
Job Objective: Oversee and coordinate all production activities within the manufacturing facility, ensuring that teams and resources are managed effectively to meet key goals surrounding efficiency, quality, safety, and output. Cultivate an optimal work environment while driving continuous process improvements.Main Responsibilities:Lead production teams by overseeing scheduling, training, motivation, and performance management of line staff.Ensure that operations are efficient and organized, adhering to all relevant procedures, standards, and regulations (GMP, FDA, ISO, OHSAS, SOX, etc.).Analyze and implement continuous improvement strategies aimed at reducing defects and scrap while enhancing yields and productivity through lean manufacturing, Six Sigma, and advanced problem-solving techniques.Ensure product traceability and quality through thorough reviews of units, routers, and labels, alongside meticulous record-keeping in manufacturing systems (SFA, SAP, Kronos, or equivalent).Manage and track key performance indicators and production metrics, preparing regular reports to communicate progress, incidents, and outcomes.Facilitate smooth shift transitions to maintain operational continuity and uphold production plans.Participate in audits, investigate non-conformities, and ensure adherence to corporate and legal EHS requirements, including relevant tasks and training.Develop and execute corrective and preventive measures related to safety, quality, efficiency, and team collaboration culture.Work closely with support departments (Engineering, Quality, Materials, HR) to set priorities, allocate resources, and execute projects.Promote a safe, positive work atmosphere that emphasizes team development, inclusion, and diversity.
General Purpose: Lead, mentor, and oversee dynamic customer service teams engaged in policy servicing operations, access and reimbursement, and global complaint management. Drive operational excellence and ensure compliance with regulations while cultivating high standards of customer, patient, and consumer satisfaction. Collaborate across departments to implement strategies that elevate the customer experience, enhance operational efficiency, and foster business growth in both local and global highly regulated environments.Key Responsibilities:Guide and develop cross-functional teams in customer service, operations, access/reimbursement, and complaint management, nurturing a culture of high performance and continuous improvement.Oversee customer support, policy servicing, call/contact centers, and complaint resolution operations, ensuring adherence to SLA, KPIs, and regulatory/global standards.Design and implement strategies to enhance customer/user experiences, initiate continuous improvement projects, and integrate technological solutions to optimize processes and outcomes.Manage data handling, performance metrics analysis, reporting, and compliance/audit processes efficiently.Create and execute operational business plans, access/reimbursement strategies, and comprehensive training programs for both internal and external teams.Maintain strong stakeholder relationships, including commercial teams, vendors, technical areas, strategic partners, and regulators across multiple countries.Ensure thorough documentation, investigation, and reporting of complaints/adverse events, and maintain communication with internal/external customers, including drafting regulatory-compliant formal responses.Encourage innovation, digital tool adoption, automation, and transformation initiatives that align with business needs and industry trends.Support and educate teams, clients, and customers on administrative, technical, and regulatory processes.Champion initiatives promoting inclusion, diversity, well-being, and talent development within the organization.
General Purpose: As a Quality Complaint Specialist, you will play a crucial role in supporting and conducting thorough investigations into complaints related to medical and pharmaceutical products. You will manage, document, and report quality events while ensuring compliance with regulatory standards, promoting continuous improvement, and achieving service excellence. This role requires collaboration with both internal and external teams, fostering a culture of inclusivity.Main Responsibilities:Investigate, analyze, and follow up on product complaints, performing functional, visual, or dimensional testing as necessary.Document all pertinent information including product history, device records, risk documentation, and labeling, while adhering to good laboratory, manufacturing, and documentation practices.Identify the root causes of complaints and perform basic statistical analysis, reporting findings to relevant teams.Recognize potentially reportable events and escalate them appropriately to the PMS Manager, Clinical Specialist, or regulatory authorities.Assist in managing Corrective and Preventive Actions (CAPAs), Non-Conformance Event Procedures (NCEPs), Out of Trend (OOT) investigations, and other compliance and improvement initiatives.Engage in continuous improvement and innovative projects related to complaint investigation processes.Utilize documentation systems (QMS, databases, tracking sheets) to monitor, track, and report outcomes efficiently.Train colleagues in processes and products as needed.Facilitate product integration and transfers between different sites.Support environmental health and safety (EHS) initiatives, ensuring proper calibration, preventive maintenance, and control of laboratory equipment.Ensure timely and effective closure of complaint investigations.Assist in communications with third parties including OEMs, Contract Manufacturers, internal clients, and various functional areas.
Join AbbVie, a global biopharmaceutical company committed to discovering and delivering innovative medicines that solve serious health issues. We are currently seeking dedicated Production Operators for a temporary contract of 6 months. The available shifts include both morning and afternoon schedules.
 As a Supplier Quality Engineer III at AbbVie, you will play a vital role in collaborating with suppliers to ensure that all materials and services meet stringent quality specifications and comply with company standards. You will maintain the integrity of our approved suppliers by documenting processes necessary to satisfy regulatory agency requirements and the QMR03 Supplier Controls policy. This position requires close coordination with various departments to achieve established goals and adhere to established procedures.Key Responsibilities:• Manage the initiation, notification, tracking, and closure of Supply Corrective Action Requests (SCARs) as the Quality Contact in the GTW system.• Monitor materials that are blocked, on hold, or quarantined to facilitate compliant material disposition aligned with business objectives. Review and approve the disposition of non-conforming materials.• Participate in the Center of Excellence (CoE) meetings focusing on supplier metrics and controls, escalating any pertinent issues, changes in corporate procedures, or CoE-managed projects to management.• Assist in executing assigned project-related activities, including supply assurance, product introductions, supplier qualifications, and supply change notifications.• Process change notifications from local and international suppliers, collaborating with the Global GSQM department and forming interdisciplinary teams to evaluate impacts across company departments.• Prepare, coordinate, and execute First Articles and Change Plans related to the evaluation of materials affected by change notifications or new qualifications.• Ensure that specifications for new material qualifications or changes are adequate for incoming materials.Additional responsibilities may include addressing deviations, non-conformance reports, corrective and preventive actions, and participating in cross-functional team meetings and internal audits.
Role Overview Experian is seeking a Business Analyst in Heredia. This position focuses on analyzing business processes and finding ways to improve them. The Business Analyst provides insights that support strategic decision-making across the company. What You Will Do Review and analyze existing business processes Identify areas where improvements can be made Deliver clear, actionable insights to support strategy Work closely with teams across different departments Help ensure solutions align with client and stakeholder needs Collaboration This role involves frequent interaction with cross-functional teams to make sure business solutions are effective and relevant.
Join Experian, a global leader in data analytics and information services, as a Senior Business Analyst. In this role, you will utilize your analytical skills to identify business needs, develop strategies, and improve operational efficiencies. You will work closely with stakeholders to gather requirements, conduct data analysis, and deliver actionable insights that drive decision-making.
Join Experian as a Senior Accounting Analyst – Revenue, where you will play a vital role in managing and analyzing revenue streams. This position demands a keen analytical mind and deep understanding of accounting principles to provide insights that drive our financial strategies.
Join AbbVie, a global biopharmaceutical company, as a Manufacturing Supervisor. In this role, you will lead a dynamic team in the production of life-changing medicines. Your expertise will guide the team in achieving operational excellence while adhering to safety and quality standards.
Join AbbVie, a global leader in biopharmaceuticals, as a Quality Engineer. In this role, you will be responsible for ensuring the highest quality standards are maintained throughout our manufacturing processes. You will collaborate with cross-functional teams to implement quality assurance strategies, conduct audits, and support compliance initiatives.
Join AbbVie as a Complaint Resolution Specialist I in our Heredia office. In this entry-level position, you will play a vital role in ensuring customer satisfaction through effective resolution of complaints. You will be responsible for responding to customer inquiries, investigating complaints, and providing timely feedback, ensuring that our clients receive the highest level of service.
Join AbbVie as a Manufacturing Engineer, where you will play a pivotal role in our production processes. We are seeking a motivated engineer with a passion for optimizing manufacturing operations and enhancing product quality. In this role, you will be responsible for the analysis and improvement of manufacturing procedures, ensuring compliance with industry standards, and collaborating with cross-functional teams to drive innovations.
Join Experian as an iOS Developer and be part of a dynamic team that is revolutionizing the way consumers interact with their financial data. In this role, you will design and implement cutting-edge mobile applications that enhance user experience and drive customer engagement.
Join AbbVie as a Complaint Processing Supervisor in Heredia, where you will play a pivotal role in ensuring customer satisfaction by efficiently managing and resolving complaints. This entry-level position offers a unique opportunity to grow within a leading biopharmaceutical company dedicated to improving patients' lives.
Join AbbVie as a Quality Complaints Specialist, where you will play a vital role in ensuring the highest quality of our products through thorough investigation and resolution of quality complaints. You will collaborate with cross-functional teams to analyze data, identify trends, and implement corrective actions to enhance quality assurance processes.
Experian is looking for a Senior Data Engineer to join the team in Heredia. This role focuses on designing, building, and maintaining scalable systems that support data-driven decision-making across the company. Role overview The Senior Data Engineer will work closely with colleagues from different departments to understand business needs and turn them into effective data solutions. The position involves shaping data architecture, developing and optimizing ETL processes, and supporting cloud-based infrastructure. What you will do Design and maintain scalable data processing systems Enhance and support data infrastructure using cloud technologies Collaborate with cross-functional teams to gather and translate requirements Optimize data workflows for quality and reliability Requirements Experience in data architecture and ETL processes Strong background in cloud technologies Analytical skills to improve data quality and workflows Ability to work effectively with teams across the business
The Senior Manager of Post-Market Complaint Operations at AbbVie oversees a team responsible for handling product complaints and supporting ongoing product quality. This position is based in Heredia and focuses on upholding safety standards and regulatory compliance after products reach the market. Role overview This leader guides the complaint operations team, ensuring that processes align with internal standards and external regulations. The role involves direct coordination with regulatory agencies and helps define strategies for post-market surveillance. Attention to detail and a commitment to patient safety are central to this work. Key responsibilities Lead and develop the team managing post-market complaint operations Drive compliance with regulatory requirements and company policies Oversee effective communication with regulatory bodies Shape strategies for monitoring product performance and safety after launch Impact This position plays a crucial role in maintaining AbbVie's standards for product safety and quality, directly supporting the company’s commitment to patients and regulatory partners.
Role Overview Experian is looking for a Senior Data Engineer with AWS expertise to join the team in Heredia. This role focuses on designing, building, and maintaining data pipelines that support analytics and operations. The position plays a key part in enabling data-driven decision-making across the company. What You Will Do Design and develop data pipelines on AWS Maintain and optimize existing data infrastructure Work closely with analytics and operational teams to deliver reliable data solutions Collaborate with colleagues from different departments to improve data processes
