The Document Control Associate I is responsible for documentation control activities including managing quality records, providing translation services between English and Spanish, and supporting Change Control system users. The role requires proficiency in various computer applications and a background in engineering or related fields, focusing on quality assurance in the healthcare industry.

The Principal Regional Leadless Specialist provides technical, clinical, educational, and sales support to drive the adoption of Abbott's leadless technology. Responsibilities include educating healthcare providers, coordinating training programs, collaborating with marketing for product feedback, and ensuring compliance with company policies. This role requires extensive travel and offers a chance to grow within a leading healthcare company.

The Quality Assurance Specialist analyzes quality standards for components and materials, applies testing methodologies, conducts inspections, and documents quality issues. They also prepare reports to recommend improvements and may liaise with external vendors.

The Senior Engineer, Continuous Improvement & Operational Excellence will analyze and implement manufacturing and business process improvements to enhance capacity, reduce lead times, and boost efficiency. Responsibilities include leading projects, providing technical mentorship, utilizing Lean manufacturing concepts, conducting capacity analyses, and driving continuous improvement initiatives while complying with quality and regulatory standards.

The TAVI Territory Manager is responsible for achieving sales and clinical objectives for the Structural Heart TAVI division, collaborating with various stakeholders to develop customer-focused strategies, managing sales processes using SFDC, and providing in-service training for product usage. The role requires significant cardiovascular sales experience and may involve extensive travel.

The Associate Director of Strategic Partnerships at Abbott will manage and establish Lingo's strategic partnerships, build relationships with senior executives, and oversee the P&L of each partnership. This role involves developing a multi-year partnerships strategy to drive customer acquisition and business growth, negotiating contracts, and leading cross-functional teams to execute partnership initiatives.

The Processing Operator at Abbott will manage the manufacturing process of nutritional products, involving physical handling of raw ingredients, operating and cleaning equipment, and maintaining quality and safety compliance. Responsibilities include using computer systems to document manufacturing steps and preparing bulk ingredients for blending operations.

The role primarily involves ensuring the implementation of quality plans during Clinical Trial processes, adhering to quality assurance regulations, writing standard operating procedures, and supporting audits. Responsibilities also include monitoring quality control during testing and operations, addressing issues related to quality and reliability, and facilitating training as needed.

The Document Control Associate II is responsible for executing documentation control activities, including managing Windchill and SAP systems, translating documentation in English and Spanish, processing quality records, and providing technical support for facility projects while ensuring effective change request administration and documentation control.

The Junior Cybersecurity Specialist is responsible for creating and maintaining threat models and risk assessments for products, focusing on security risks, patient safety, and data protection. The role involves collaboration on product security initiatives, documentation, and proactive vulnerability management.

As a Product Manager, you will develop and execute the product roadmap for data sharing solutions between Abbott and its healthcare partners, focusing on enhancing the FreeStyle Libre platform. Your role will involve collaboration with multiple teams to define user requirements and track the impact of product launches.

The Operator 1 position involves performing electronic assembly, casting/coating, mechanical assembly, and packaging of medical devices. Responsibilities include inspecting and repairing devices using tools and equipment, maintaining production standards, and complying with regulatory requirements.

As a Software Engineer II at Abbott, you will develop and enhance web-based software applications primarily for the Cardiometabolics/Informatics team. Responsibilities include designing solutions, coding, debugging, and testing software in alignment with Agile/Scrum methodologies. Collaboration with team members to meet project goals is essential.

The Operator 1 position involves performing electronic, mechanical, and packaging assembly of medical devices, correcting issues with production parts, and ensuring compliance with regulatory standards. Duties include using specialized tools for assembly and inspection, along with packaging products accurately. The operator will work with precision instruments in a controlled environment, adhering to strict quality and safety protocols.

The Operator I role involves performing electronic assembly, mechanical assembly, casting/coating operations, and packaging of medical devices. Responsibilities include using microscopes and specific tools for assembly, repairing defects, ensuring compliance with FDA regulations, and conducting inspections. Employees can expect to engage in hands-on tasks requiring dexterity and attention to detail in a clean-room manufacturing environment.

The Quality Systems Engineer II will support quality system processes, implement data analysis, investigate system nonconformances, ensure compliance with quality regulations, and lead teams to improve product quality. The role involves collaborating with product development and production engineers to meet quality deliverables and managing quality audits.

The Operator I position involves performing assembly, welding, x-ray, repair, and testing operations on medical devices like pacemakers and defibrillators under close supervision. The role requires adherence to standardized procedures and involves working in the Cardiac Rhythm Management division.

As an Operator I, you will perform electronic assembly functions, mechanical assembly functions, and packaging of medical devices. Responsibilities include inspecting, repairing, and testing units as well as complying with FDA regulations and Quality Management Systems. You will need to interact with colleagues and maintain equipment in a clean-room manufacturing environment.

The Field Marketing Manager will drive marketing campaigns, collaborate with the sales team, ensure product understanding and adoption, and analyze campaign success in the Electrophysiology division. Responsibilities include content creation, training local teams, maintaining communications, and engaging with KOLs to promote Abbott EP products within the Central Atlantic territory.

The Senior Territory Manager for Electrophysiology will be responsible for increasing revenue and market share in assigned accounts, developing professional relationships, generating new business, and creating detailed business plans. They will understand the healthcare reimbursement landscape to enhance customer value and foster long-term partnerships.