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Currently tracking 36 active AI roles, up 67% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $58k–$345k (avg $175k).

Hiring
36 / 37
Momentum (4w)
↑+176 +67%
438 opens last 4w · 262 prior 4w
Salary range · avg $175k
$58k–$345k
USD · disclosed roles only
Tracked since
Nov '25
last role yesterday
Hiring velocityscroll left for older weeks
1 new role
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Jobs (885)

36 AI · 626 total active
Show
Active onlyAI only (≥ 7)
Stage
AllData · 14Post-train · 3Serve · 1Agent · 28Eval Gate · 1Ship · 5
Function
AllEngineering · 515Product · 287Research · 83
Country
AllUnited States · 527China · 68Germany · 48India · 42Ireland · 41Japan · 28France · 26Mexico · 12Turkey · 11Taiwan · 9Italy · 8Netherlands · 8Puerto Rico · 7Spain · 7Austria · 6Canada · 6Australia · 4Hungary · 4Brazil · 3Portugal · 3South Korea · 3Czech Republic · 2Malaysia · 2Saudi Arabia · 2Switzerland · 2United Kingdom · 2Norway · 1Qatar · 1Singapore · 1Sweden · 1United Arab Emirates · 1
Sort
AI scoreRecentTitle
TitleStageFunctionLocationFirst seenAI score
Supervisor - Peptide Manufacturing Operations
Supervisor for Peptide Manufacturing Operations at Eli Lilly, responsible for managing day-to-day production activities in a new advanced manufacturing facility. The role focuses on safety, quality, regulatory compliance, and team supervision within API synthesis and purification.
—EngineeringLebanon, IN2w ago0
Process Technician - Material Prep/Formulation/Filling (Night Shift)
Process Technician role at Eli Lilly focused on operating highly automated equipment for material preparation, formulation, and filling in a night shift capacity. Requires adherence to Good Manufacturing Practices and safety standards, with opportunities for cross-training and supporting leadership in troubleshooting and training.
—EngineeringUS: Research Triangle Park, NC2w ago0
Senior Director Regulatory Strategy
Senior Director of Regulatory Strategy at Eli Lilly, focusing on gene-editing programs in early development. Responsibilities include planning, developing, and implementing regulatory strategy, submissions, and compliance activities to support regulatory approvals. The role involves leading regulatory affairs for assigned programs, interacting with global health authorities, and ensuring compliance with regulatory standards.
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Product
Boston, MA
2w ago
0
Pharmaceutical Sales- Territory Manager- Dermatology Specialty
Pharmaceutical Sales Territory Manager for Dermatology Specialty at Eli Lilly. Responsible for account-based selling to healthcare providers, building relationships, and driving adoption of therapies. Requires understanding of territory and reimbursement landscape, strong selling skills, and execution of sales activities. Basic qualifications include a Bachelor's degree and a valid driver's license. Preferred qualifications include sales experience, account-based selling, and dermatology sales experience.
—ProductFort Worth, TX2w ago0
Senior/Principal Scientist, Bioprocess Purification Development
This role focuses on the development and optimization of purification processes for bioproduct active pharmaceutical ingredients. It involves experimental design, process transfers, and authoring regulatory documents within a healthcare/pharmaceutical context. The role requires a background in chemical engineering or biochemistry and experience in purification development.
—EngineeringIndianapolis, IN2w ago0
Pharmaceutical Sales - Territory Manager - Neuroscience Specialty
This is a pharmaceutical sales role focused on promoting Alzheimer's disease treatments within a specific territory. The role involves managing accounts, driving brand strategies, educating healthcare providers, and influencing care ecosystems. While it mentions leveraging 'data driven approach and other technologies', the core function is sales and account management, not AI/ML development.
—ProductFayetteville, NC2w ago0
Process Controls and Instrumentation Technician
This role is for a Process Controls and Instrumentation Technician at Eli Lilly's new Gene Therapy manufacturing facility. The technician will be responsible for the maintenance, calibration, troubleshooting, and installation of process instrumentation (Temperature, Pressure, Flow, Control Valves) to ensure equipment compliance with cGMP and operational readiness for clinical and commercial supply. The role involves supporting startup activities, preventive and corrective maintenance, documentation, and collaboration with various site teams.
—EngineeringLebanon, IN2w ago0
Principal Scientist, Large Molecules Mass Spectrometry
This role focuses on applying mass spectrometry techniques to characterize the pharmacokinetic, biotransformation, and biodistribution properties of therapeutic proteins and genetic medicine modalities in preclinical animal models within the Bioanalytical Research Group at Eli Lilly. It involves developing and implementing LC/MS approaches and collaborating with project teams. The role requires a Master's or Bachelor's degree in a relevant scientific field with significant work experience in protein and oligonucleotide mass spectrometry and bioanalysis.
—ResearchIndianapolis, IN2w ago0
Scientist - Industrial Hygiene HSE
Scientist role focused on Industrial Hygiene and Health, Safety, and Environment (HSE) compliance within a pharmaceutical manufacturing facility. Responsibilities include developing and managing IH programs, ensuring compliance with regulations and best practices, providing technical support, and influencing risk reduction strategies. Requires a Bachelor's degree in a scientific or engineering discipline, prior IH experience, and CIH certification.
—EngineeringUS: Research Triangle Park, NC2w ago0
Pharmaceutical Sales- Associate Territory Manager- Cardiometabolic Health
This is a pharmaceutical sales role focused on selling cardiometabolic health products to healthcare providers. The role involves account-based selling, understanding the market, and utilizing company models to drive results. It mentions the integration of AI company-approved tools to streamline customer interactions, but AI is not the core craft of the role.
—ProductSpartanburg, SC2w ago0
Qualified Person (QP) - (m/w/d)
The Qualified Person (QP) is responsible for certifying that each batch of a medicinal product meets all required provisions when released from a manufacturing facility, ensuring compliance with GMP, marketing authorization, and current regulations. This role involves continuous quality and regulatory monitoring, analysis of corporate standards, participation in regulatory updates, and oversight of imported products.
—ProductAlzey, Germany2w ago0
(Sr.) Medicines Quality Manager
This role is for a Medicines Quality Manager at Eli Lilly in China, focusing on implementing and maintaining quality systems (SEQS) for drug development and medical affairs. Responsibilities include ensuring compliance with global and local regulations, managing audits and inspections, driving quality improvement initiatives, and providing quality oversight. The role requires experience in quality systems within a regulated environment (GxPs, ICH) and strong communication and influencing skills.
—ProductShang Hai-上海, China2w ago0
Sr Brand Manager - Alzheimer's Disease Diagnostics
This role is for a Sr. Brand Manager focused on diagnostic and innovation readiness for Alzheimer's disease at Eli Lilly. It involves market understanding, content development, tracking execution for the diagnostic field force, engaging thought leaders, and managing external partnerships. The role requires collaboration to execute commercial activities critical to future innovations.
—ProductShang Hai-上海, China2w ago0
医药代表-心血管代谢健康事业部
This role is for a pharmaceutical sales representative focused on promoting and selling company products within a specific territory in the cardiovascular and metabolic health division. Responsibilities include achieving sales targets, building and maintaining customer relationships, providing product information, gathering market intelligence, and collaborating with internal teams.
—ProductBin Zhou-滨州, China2w ago0
Sr. Director / Executive E&C Core Capabilities
This role is for a Sr. Director/Executive Director of E&C Core Capabilities at Eli Lilly in Shanghai, China. The primary function is to serve as a senior Ethics and Compliance (E&C) Business Partner, providing expert leadership in managing E&C risks and advising on program design, process controls, and risk management. The role involves leading Centers of Excellence for Monitoring & Data Intelligence and Third-Party Organization (TPO) Management, and partnering with business leaders to strengthen controls through risk-based oversight and data-driven insights. The ideal candidate will have over 10 years of experience in ethics and compliance within highly regulated industries, strong analytical capabilities, and the ability to influence senior leaders. Fluency in Mandarin and English is required.
—ProductShang Hai-上海, China2w ago0
Advisor/ Sr. Advisor - Preclinical Discovery, Women's Health - Preeclampsia
This role focuses on discovery research in preclinical women's health, specifically preeclampsia, involving target identification, hypothesis development, and advancing preclinical biology. It requires a PhD in a related field and hands-on laboratory experience with in vitro, ex vivo, and in vivo models.
—ResearchBoston, MA2w ago0
Associate Director - Engineering - Process (Small Molecule)
Associate Director of Process Engineering for a new Small Molecule API manufacturing facility. Responsibilities include hiring and developing a team of process engineers, establishing business systems and processes for GMP operations, and overseeing engineering deliverables for facility startup and ongoing production. Requires a BS in Chemical Engineering or related field with extensive API/chemical manufacturing experience.
—EngineeringHouston, TX2w ago0
Expert Maintenance Technician - Lilly Medicine Foundry
This role is for an Expert Maintenance Technician at Eli Lilly's new Medicine Foundry, a center for advanced manufacturing and drug development. The technician will be responsible for maintaining and repairing manufacturing and facilities equipment, ensuring optimal performance and compliance with GMP and safety regulations. The role involves multi-craft expertise in mechanical, electrical, and instrumentation, troubleshooting, documentation, and potentially leading a team. It is a critical role in ensuring the efficient and compliant operation of a state-of-the-art pharmaceutical manufacturing facility.
—EngineeringIndianapolis, IN +12w ago0
Maintenance Supervisor - Lilly Medicine Foundry
This role oversees maintenance activities for a new advanced manufacturing and drug development center, ensuring equipment availability, reliability, and optimal performance in compliance with cGMP and other standards. The Maintenance Supervisor leads and develops the maintenance team, fostering a culture of safety, technical expertise, and innovation, while aligning maintenance programs with organizational goals for safety, quality, and efficiency.
—EngineeringLebanon, IN +12w ago0
Director - Experienced Discovery Toxicology Project
This role leads discovery toxicology projects for pharmaceutical small molecule products, involving the design, execution, and interpretation of toxicology studies. The position requires a PhD or MS/BS with extensive experience in toxicology and a strong understanding of the drug discovery and development process, including regulatory guidelines.
—EngineeringIndianapolis, IN2w ago0
Brand Manager – HCP Digital & Pharmacy Ecosystem | Cardiometabolic Health
Brand Manager for Cardiometabolic Health in Portugal, focusing on pharmacy channel strategy and digital/omnichannel HCP engagement. The role aims to improve patient access and continuity of care by integrating pharmacy and digital strategies, building relationships with healthcare partners, and optimizing engagement through customer journeys and insights. Requires cross-functional collaboration, budget management, and proficiency in digital tools and AI.
—ProductLisbon, Portugal2w ago0
Sr. Principal Architect-Data - MQ IT
This role is for a Sr. Principal Architect-Data at Eli Lilly, focusing on defining, designing, building, and maintaining the data architecture vision and strategy for a manufacturing site. Responsibilities include setting data standards, data modeling, data warehousing, data integration, data governance, and ensuring data security and cloud architecture principles. The role requires extensive experience in data modeling, statistical methods, ontology development, and working with various database technologies and cloud platforms.
—EngineeringPleasant Prairie, WI2w ago0
Operator – Parenteral Manufacturing
Operator role in parenteral manufacturing at Eli Lilly, focusing on supporting operational activities including formulation, aseptic filling, and equipment preparation. Responsibilities include ensuring safety, quality, and productivity, troubleshooting, training, and collaborating cross-functionally to maintain the supply of medicines.
—EngineeringKenosha, WI2w ago0
Advanced in Vitro Models - Advisor/Sr. Advisor 
Seeking a scientist to develop and apply advanced in vitro models (co-culture systems, iPS-derived cells, spheroids, organoids, organ-on-a-chip) or new approach methodologies (NAMs) to address mechanistic/investigative toxicology questions in drug discovery. The role involves qualifying novel assays, investigating mechanisms of compound-induced toxicity, and collaborating with external partners.
—ResearchIndianapolis, IN2w ago0
Associate Director - Joint Process Team Lead
Associate Director role focused on leading cross-functional teams for contract manufacturing of new modalities (Gene Therapy) in a pharmaceutical setting. Responsibilities include developing and implementing quality and supply plans, managing production schedules, resolving supply chain issues, ensuring regulatory compliance, and serving as a liaison between Eli Lilly and contract manufacturers. Requires experience in pharmaceutical manufacturing, technical support, quality assurance, and managing external relationships.
—ProductLebanon, IN2w ago0
Senior / Principal Associate QA API External Manufacturing
This role is for a Senior / Principal Associate QA API External Manufacturing at Eli Lilly, focusing on ensuring the quality and compliance of externally manufactured Active Pharmaceutical Ingredients (APIs) according to cGMP regulations and company standards. Responsibilities include serving as a QA point of contact for external sites, reviewing manufacturing documentation, leading audits, overseeing quality events, and collaborating with internal teams.
—EngineeringIndianapolis, IN2w ago0
Analytical Technical Steward Peptides and Oligonucleotides
This role focuses on the analytical testing of peptides and oligonucleotides in a pharmaceutical manufacturing setting. Responsibilities include reviewing and releasing data from contract manufacturers, investigating out-of-specification results, performing method validation, and ensuring compliance with regulatory expectations. The role requires a strong background in GMP laboratory practices and analytical techniques.
—EngineeringIndianapolis, IN2w ago0
Senior Principal Chemist
Senior Principal Chemist role in Pharmaceutical Investigations Team, focusing on analytical testing of drug substances, drug products, and other materials. Responsibilities include foreign/unknown material analysis, counterfeit/tampering investigations, and supporting legal initiatives using various analytical techniques and IT tools. Requires expertise in physical and chemical analytical techniques, good documentation practices, and strong communication skills.
—EngineeringIndianapolis, IN2w ago0
Formulation/Equipment Prep Ops Nights
This role is for a Production Technician at Eli Lilly's Parenteral Manufacturing site, responsible for preparing equipment and formulating products for sterile filling. It requires adherence to safety policies, SOPs, and GMPs, with basic math and computer skills. Experience in GMPs, formulation, and/or equipment prep is preferred.
—EngineeringIndianapolis, IN2w ago0
Technician - Process Quality Assurance Floor Support (Night Shift)
Quality Assurance Floor Support Specialist role at Eli Lilly, focusing on GMP operations in pharmaceutical manufacturing. Responsibilities include QA oversight, documentation review, sample collection, and system support in a night shift environment.
—EngineeringUS: Research Triangle Park, NC2w ago0
Metabolic Account manager-
Account Manager for cardiometabolic products in Denmark, responsible for territory management, customer engagement, and coaching team members on sales capabilities. Utilizes data, AI, and customer insights for account planning and maximizing business potential.
—ProductDenmark, Remote2w ago0
Alternance 12 mois - Graphiste - F/H
This is a graphic designer role focused on creating visual content, including logos, graphics, and animations for internal communications, congress videos, and health professional information. The role involves modifying existing projects in After Effects and Premiere Pro, adapting PowerPoint presentations into animations, and designing elements for live broadcasts. While the role mentions an interest in new technologies and AI, its core function is graphic design and video content creation, not AI/ML development.
—ProductNeuilly Sur Seine, France2w ago0
医药代表-心血管代谢健康事业部
This role is for a pharmaceutical sales representative focused on promoting and selling company products within a specific territory in the cardiovascular and metabolic health division. Responsibilities include achieving sales targets, building and maintaining customer relationships, providing product information, and gathering market intelligence. A bachelor's degree in a pharmaceutical-related field and prior sales experience are preferred.
—ProductShao Yang-邵阳, China2w ago0
医药代表-心血管代谢健康事业部
This role is for a pharmaceutical sales representative focused on promoting and selling company products within a specific territory in the cardiovascular and metabolic health sector. Responsibilities include achieving sales targets, building and maintaining client relationships, providing product information, and gathering market intelligence. Requires a bachelor's degree in a relevant field and prior pharmaceutical sales experience is preferred.
—ProductHang Zhou-杭州, China2w ago0
Master Planner
This role is a Master Planner responsible for creating and managing production plans, inventory, and material requirements within SAP for a pharmaceutical manufacturing facility. It involves close collaboration with regulatory, production, and quality departments to ensure compliance and optimize capacity, with a focus on meeting demand while minimizing inventory costs. The role also includes managing change control and reporting on key supply chain metrics.
—ProductSuzhou Manufacturing-苏州工厂, China2w ago0
Advisor – Gene Therapy Discovery & Platform Research, Analytical Development
This role focuses on developing analytical methods and supporting gene therapy pipeline progression at Eli Lilly. It involves assay development, characterization of viral proteins, AAV vector design, and analytical support for vector core groups. The position also requires expanding analytical capabilities and coaching junior scientists.
—ResearchBoston, MA2w ago0
Process Engineer – Shift Technical Support
Process Engineer role focused on supporting and improving manufacturing processes, equipment, and facilities in a pharmaceutical (healthcare) setting. Responsibilities include troubleshooting, cross-functional collaboration, process support, equipment monitoring, safety basis development, and utilizing modeling/simulation for process understanding. Requires a BS in Engineering and experience in chemical manufacturing.
—EngineeringLebanon, IN2w ago0
Development Engineer, Drug-Device Combination Products (ddCP)
Development Engineer for Drug-Device Combination Products (ddCP) at Eli Lilly, responsible for executing design control activities, device-drug integration studies, and combination product development to support clinical and commercial programs. This role involves risk management, design control execution, integrated control strategy development, stability study design, and regulatory submission support within a regulated healthcare environment.
—EngineeringIndianapolis, IN2w ago0
Utilities Operations Supervisor - Lilly Medicine Foundry
Oversees utility operations for a new advanced manufacturing and drug development center, ensuring safe and uninterrupted generation and distribution of utility services. Responsibilities include direct supervision of operators, troubleshooting, problem-solving, and implementing improvements within utility systems (water, air, steam, etc.). The role focuses on safety, quality, operational excellence, and people development within a regulated manufacturing environment.
—EngineeringLebanon, IN +12w ago0
Associate Director - Medical Science Liaison - Gastroenterology- Dallas TX
This role is for a Medical Science Liaison in Gastroenterology at Eli Lilly. The primary focus is on scientific and clinical expertise, engaging with healthcare professionals to provide and gather information about therapeutic areas and Lilly's compounds. The role involves continuous learning, customer engagement, territory ownership, and strategic communication of insights.
—ProductDallas, TX2w ago0
Associate Director - Business Solutions IT Project Lead
Associate Director - Business Solutions IT Project Lead at Eli Lilly, responsible for deploying IT systems architecture for a new manufacturing site, managing major initiatives across Supply Chain, Logistics, Manufacturing, and Finance. Requires 7+ years of IT project leadership experience and a Bachelor's degree. Manufacturing IT systems knowledge and understanding of GMP/FDA regulations are preferred.
—EngineeringPleasant Prairie, WI2w ago0
Associate Director- Medical Science Liaison - Cardiometabolic Health- Colorado
This role is for a Medical Science Liaison in the Cardiometabolic Health field. The primary responsibilities include engaging with healthcare professionals to provide and gather scientific and clinical information, acting as a liaison between Lilly and the scientific community, and contributing to Lilly's strategic direction. The role requires advanced scientific knowledge, strong communication and presentation skills, and the ability to manage a territory effectively.
—ProductDenver, CO2w ago0
Pharmaceutical Sales - Territory Manager - GI Specialty
Pharmaceutical Sales Territory Manager for Eli Lilly's GI specialty, responsible for account-based selling to healthcare providers, building relationships, and driving adoption of therapies. Requires a Bachelor's degree, sales experience, and strong business acumen.
—ProductFargo, ND2w ago0
Ingeniero Junior de Garantía de Calidad
Junior Quality Assurance Engineer role at Eli Lilly, a global healthcare leader. The role focuses on monitoring GMP services, participating in qualification/validation projects for GMP equipment and systems, ensuring quality standards are met for facilities, services, equipment, and control systems (ISA 95 level 1). It also involves providing technical and quality advice for continuous improvement and ensuring systems remain validated throughout their lifecycle. No prior experience is required, but pharmaceutical sector internships are a plus. Fluency in English (C1) is mandatory. Key personal skills include teamwork, customer orientation, decision-making, strong communication, organization, attention to detail, knowledge of Good Manufacturing Practices (GMP), quality concepts in the pharmaceutical industry, and common IT tools.
—EngineeringAlcobendas, Spain2w ago0
Administrativo de Datos Junior
Junior Data Administrator role focused on maintaining master data (GMP and business) for a manufacturing plant using SAP and other systems. Responsibilities include data entry, cleaning, verification, and supporting optimization and incident resolution. Requires technical training in administration/finance and user-level computer skills, with Excel/Office proficiency. SAP knowledge is desirable.
—EngineeringAlcobendas, Spain2w ago0
Post-doctoral Biologist
Post-doctoral Biologist role at Eli Lilly focused on discovering and advancing peptide and antibody drugs. Responsibilities include developing rodent models, executing in vivo studies, performing cell culture and assays, analyzing data, and collaborating with internal and external teams. Requires a Ph.D. in Biology, proficiency in in vivo studies, and experience with small animal surgery and cell-based assays.
—ResearchIndianapolis, IN2w ago0
Lead Maintenance Planner
The Lead Maintenance Planner at Eli Lilly is responsible for improving equipment reliability and productivity by planning and scheduling maintenance activities. This role involves managing work orders, ensuring spare parts availability, coordinating with vendors, and utilizing a CMMS like Maximo. The position is in a manufacturing facility startup environment, with a transition from initial spare parts coordination to full-time planning and scheduling.
—EngineeringLebanon, IN2w ago0
Process Control and Automation Engineer (I&C)
This role is for a Process Control and Automation Engineer in a pharmaceutical manufacturing facility. Responsibilities include supporting and enhancing automation platforms, troubleshooting process interruptions, field device diagnostics, and ensuring the safe design and operation of new equipment. The role requires experience in industrial equipment control, API manufacturing process control, and utilities/environmental control systems, with a preference for Delta-V and Rockwell Automation Systems.
—EngineeringLebanon, IN2w ago0
Mechanic A-IDAP
Maintenance Mechanic for pharmaceutical manufacturing equipment including UV curing, vision systems, laser marking stations, conveyors, and robotics. Responsibilities include machine maintenance, setup, condition monitoring, troubleshooting, developing repair part lists, and proactive reliability planning within a regulated industry.
—EngineeringIndianapolis, IN2w ago0
Operator - Device Assembly & Packaging - FDE (Fixed Duration Employment) - $3,000 Sign-on Bonus - Starting at $22/hour + Benefits - Night/Day Shift
Operator role focused on assembly and packaging of medical devices in a regulated manufacturing environment. Responsibilities include operating equipment, adhering to SOPs and cGMP, documenting processes, and ensuring product quality and safety. This is a fixed-duration employment role.
—EngineeringIndianapolis, IN2w ago0