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Reporting to the Engineering Manager, the SQE II QA Automation Engineering for mobile products will participate as part of a highly skilled software development team to accelerate the automation of our mobile products’ end-to-end testing capabilities (both iOS and android).

The Role DNS Engineer – SRE is a high-impact role responsible for the architecture, scalability, and reliability of the mission-critical DNS infrastructure powering our ISP and core network services.

Responsibilities • Own the product experience and delivery for identity services, including authentication, authorization, and user lifecycle management • Drive frictionless IDM customer experience with future thinking scalability, across B2C, Mobile, and B2B. • Deliver core capabilities such as MFA, passwordless authentication, and account recovery • Partner closely with Engineering, Security, Legal, and User Design teams to balance user experience, risk, and regulatory requirements • Lead multiple cross functional teams to adopt new authentication platforms • Work with cross functional teams to design, develop, and market the product to ensure a successful delivery • Define and monitor key metrics to ensure business value is achieved • Write business & product requirements, detailed user stories and acceptance criteria • Manage product backlog including prioritization and scope for development sprint and release planning • Provide subject matter expertise on your portfolio at a granular level to the development teams and a higher level to the entire organization. • Drive continuous improvement through A/B testing, data analysis, and user feedback Qualifications • 5+ years of product management experience, preferably in customer facing digital products for multiple user roles and segmentations • Familiar with identity and access management concepts such as authentication vs. authorization, role-based access control, SSO and MFA • Proven ability to define strategy, empathize with users, prioritize effectively, and deliver complex initiatives • Demonstrated proficiency in agile framework and Product Owner responsibilities • Broad fluency across product management, business development, software and hardware engineering, UX/UI, sales and Marketing • Demonstrated proficiency in AI and automation tools to accelerate day-to-day work • Strong analytical, data interpretation, problem solving and time management skills • Demonstrated ability to facilitate communications both technical and non-technical, across functional teams • Seasoned knowledge in telecom including broadband, video, and mobile technologies • Exceptional interpersonal/people skills including verbal and written communications skills, including listening and presentation skills • Ability to be detail oriented but also able to summarize simply and concisely • Familiarity with AI Tools and AI First mindset At Optimum, every action and interaction we take part in, is driven by our three Guiding Principles: Do What’s Right, Drive One Optimum, and Make It Happen.

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What You Bring • 4+ years of experience in applied machine learning, with a focus on natural language processing or generative AI . • Hands-on experience fine-tuning and evaluating LLMs using modern tools and open-source libraries. • Strong understanding of prompt engineering, embedding-based retrieval , and evaluation strategies for generative applications. • Experience using ML tooling to lead the end-to-end lifecycle of model development—from data exploration to deployment-ready artifacts. • Track record of building user-facing AI features , especially where privacy, latency, and usability are critical. • Clear communication skills and ability to collaborate with multi-functional partners on a distributed team. • Commitment to our values: • Welcoming differences • Being relationship-minded • Practicing responsible participation • Having grit Bonus Skills • Familiarity with on-device model optimization or privacy-preserving ML. • Experience working in a browser context or with web technologies. • Contributions to open-source ML frameworks or model hubs.

Job Senior Control Systems Engineer LOCATION COMPANY JOB FIELD JOB TYPE JOB ID FLEXIBLE WORK OPTIONS LOCATION COMPANY JOB FIELD JOB TYPE JOB ID FLEXIBLE WORK OPTIONS Apply now Now hiring!

Discover more about the HelloFresh Group " pha-phslide-prev-arrow=" " data-ph-id="ph-widget-element-1647270873971-19"> Culture at HelloFresh No matter what neighborhood we happen to call home, HelloFresh employees all share the same values.

Own the hands-on execution of moving designs from Figma into production code, drawing on deep past experience of launching and maintaining systems in real-world codebases. + Incorporate AI into the design workflow.

The Distribution Specialist – Gas functions as a trainer for administrative personnel and as a task owner for claims, mapping corrections and other key operations support functions.

Essential Duties and Responsibilities Provides analytical support to various business units in the development and reporting of budgets, forecasts, investments and other related processes.

Operational Excellence • Technically lead and oversee the work of Site Area leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications. • Lead/ Participate in design reviews and DeltaV application software reviews, attend equipment and software FATs • Lead a team of automation engineers supporting commissioning • Provide periodic status updates to Project Management • Devising functional requirements and process control strategies for control systems in collaboration with Process Engineering • DCS and SCADA software design, coding/ configuration and testing (sequence logic, graphics, batch software etc.) • Perform automation engineering activities including design, tuning and troubleshooting of control loops • Implement and support electronic systems (such as plant historians, applications and software integration) used to capture process automation related production data • Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation • Automation support for capital projects including new product introductions • Promoting the use of automation to improve productivity, operational efficiency and compliance • Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed Organizational Capability • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products. • Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines. • Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement • Demonstrated ability to influence peers and business partners • Good written and verbal communication skills for both technical and non-technical audiences • Knowledge of GMP, regulatory requirements, computer system validation Basic Requirements • Minimum B.S. in Engineering and experience in Automation Engineering, preferably in Small Molecule API manufacturing. • A minimum of 2 + years working experience in Biopharma engineering, operations, or manufacturing. • Qualified applicants must be authorized to work in the United States on a full-time basis.

Operational Excellence • Technically lead and oversee the work of Site A rea leads and System Integrator s including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications. • Lead/ Participate in design reviews and DeltaV application software reviews , att end equipment and software FATs • Lead a team of automation engineers supporting commissioning • Provide periodic status updates to Project Management • Devising functional requirements and process control strategies for control systems in collaboration with Process Engineering • DCS software design, coding/ configuration and testing (sequence logic, graphics, batch software etc.) • Automation Engineering including design, tuning and troubleshooting of control loops • Implement and support electronic systems (such as plant historians) used to capture process automation related production data • Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation • Automation support for capital projects including new product introductions • Promoting the use of automation to improve productivity, operational efficiency and compliance • Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed Organizational Capability • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products. • Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines. • Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement • Demonstrated ability to influence peers and business partners • Good written and verbal communication skills for both technical and non-technical audiences • Knowledge of GMP, regulatory requirements, computer system validation Basic Requirements • Minimum B.S. in Engineering and experience in Automation Engineering , preferably in major pharmaceutical manufacturing. • A minimum of 2+ years working experience in Biopharma engineering, operations, or manufacturing. • Qualified applicants must be authorized to work in the United States on a full-time basis.

Operational Excellence • Technically lead and oversee the work of Site A rea leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications. • Lead/ Participate in design reviews and DeltaV application software reviews , att end equipment and software FATs • Lead a team of automation engineers supporting commissioning • Provide periodic status updates to Project Management • Devising functional requirements and process control strategies for control systems in collaboration with Process Engineering • DCS software design, coding/ configuration and testing (sequence logic, graphics, batch software etc.) • Automation Engineering including design, tuning and troubleshooting of control loops • Implementing and supporting electronic systems (such as plant historians) used to capture process automation related production data • Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation • Automation support for capital projects including new product introductions • Promoting the use of automation to improve productivity, operational efficiency and compliance • Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed Organizational Capability • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products. • Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines. • Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement • Demonstrated ability to influence peers and business partners • Good written and verbal communication skills for both technical and non-technical audiences • Knowledge of GMP, regulatory requirements, computer system validation Basic Requirements • Minimum B.S. in Engineering and experience in Automation Engineering , preferably in major P harmaceutical manufacturing handling Laboratory and Analytical systems and equipment, and Systems Integration and 8 + years working experience in Biopharma engineering, operations, or manufacturing. • Experience in commissioning, qualifying and supporting Analytical equipment such as cell counters, environment al testing, filter testing, etc. • Qualified applicants must be authorized to work in the United States on a full-time basis.

Operational Excellence • Technically lead and oversee the work of Site A rea leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications. • Lead/ Participate in design reviews and Automation application software reviews , att end equipment and software FATs • Lead a team of automation engineers supporting commissioning • Provide periodic status updates to Project Management • Devising functional requirements and process control strategies for control systems in collaboration with Process Engineering • DCS software design, coding/ configuration and testing (sequence logic, graphics, batch software etc.) • Automation Engineering including design, tuning and troubleshooting of system integration across platforms and sites • Implementing and supporting electronic systems (such as plant historians) used to capture process automation related production data • Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation • Automation support for capital projects including new product introductions • Promoting the use of automation to improve productivity, operational efficiency and compliance • Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed Organizational Capability • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products. • Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines. • Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement • Demonstrated ability to influence peers and business partners • Good written and verbal communication skills for both technical and non-technical audiences • Knowledge of GMP, regulatory requirements, computer system validation Basic Requirements • Minimum B.S. in Engineering and experience in Automation Engineering , preferably in major pharmaceutical manufacturing handling System integration of applications, systems and platforms • 8+ years working experience in Biopharma engineering, operations, or manufacturing. • Qualified applicants must be authorized to work in the United States on a full-time basis.

Operational Excellence • Technically lead and oversee the work of Site A rea leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications. • Lead/ Participate in design reviews and DeltaV application, Laboratory and Analytical equipment application reviews , att end equipment and software FATs • Lead a team of automation engineers supporting commissioning • Provide periodic status updates to Project Management • Devising functional requirements and process control strategies for control systems in collaboration with Process Engineering • DCS software design, coding/ configuration and testing (sequence logic, graphics, batch software etc.) • Automation Engineering including design, tuning and troubleshooting of control loops • Implementing and supporting electronic systems (such as plant historians) used to capture process automation related production data • Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation • Automation support for capital projects including new product introductions • Promoting the use of automation to improve productivity, operational efficiency and compliance • Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed Organizational Capability • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products. • Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines. • Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement • Demonstrated ability to influence peers and business partners • Good written and verbal communication skills for both technical and non-technical audiences • Knowledge of GMP, regulatory requirements, computer system validation Basic Requirements • Minimum B.S. in Engineering and experience in Automation Engineering , preferably in major P harmaceutical manufacturing handling Laboratory and Analytical systems and equipment, and Systems Integration. and minimum of 2 + years working experience in Biopharma engineering, operations, or manufacturing. • Experience in commissioning, qualifying and supporting Analytical equipment such as cell counters, environment al testing, filter testing, etc. • Qualified applicants must be authorized to work in the United States on a full-time basis.

The Senior Principal Engineer - Automation Engineering will work as a member of the Automation Engineering Department at Eli Lilly, Foundry.

If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. • The Associate Director, Oncology Discovery Contracting in the Business Operations team serves as a recognized contracting, internal business process and S2P partner within the Early Phase Oncology organization, supporting drug discovery and development through the drafting, negotiation, and management of complex procurement-facing agreements.

Responsibilities • Design and synthesize oligonucleotides and novel nucleotide analogs for incorporation into siRNA and ASO platforms to support portfolio drug discovery efforts Independently identify critical scientific questions and develop well-reasoned chemistry strategies for enhancing the potency, safety, and durability of oligonucleotide drug molecules • Collaborate with in vitro and in vivo biologists to evaluate new biological targets of interest, integrating cross-functional information to support data-driven decisions • Design and implement chemistry strategies for delivery of oligonucleotide medicines to tissues and cell types of interest, anticipating and managing risk to minimize impact on project timelines • Develop and test new ideas and apply innovative solutions that significantly advance scientific and/or project understanding across multiple drug modalities, including oligonucleotides, antibody-oligonucleotide conjugates, and peptide-oligonucleotide conjugates • Build a diverse cross-functional and external network to understand how different fields contribute to oligonucleotide research and development Focus on defining clear scientific hypotheses, goals, critical success factors, and timelines in support of advancing the portfolio • Mentor and develop junior scientists, providing constructive feedback and encouraging a culture of excellence and knowledge sharing Bring authentic scientific perspective and create a safe environment for colleagues to share ideas and contribute Represent genetic medicine project teams in presentations to departmental and cross-functional senior leadership teams Basic Qualifications • Ph.D. in organic chemistry, or a related field with 0–5+ years of experience in the pharmaceutical industry or relevant postdoctoral training Additional Skills/Preferences • Strong proficiency in synthetic organic chemistry, including design and execution of multistep synthetic routes to small molecule targets Expertise in characterization of small molecules using NMR spectroscopy, mass spectrometry, and HPLC • Experience with oligonucleotide synthesis using automated synthesizers (e.g., Mermade or K&A platforms) and downstream oligonucleotide processing is desirable but not required • Experience with conjugation of biomolecules is desirable but not required Demonstrated ability to think creatively, try new ideas, and apply findings in a fast-paced discovery environment • Familiarity with ChemDraw, electronic notebook software, and Microsoft Office Additional Information Travel 0–10% Location On-site, Indianapolis, IN – Lilly Corporate Center (LCC) Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions.

BMS, PLCs, Remote IO) OSI PI Asset Frame design and build Other OSI PI related solutions such as PI Vision • Implement and support electronic systems (such as plant historians) used to capture process automation related production data • Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation • Automation support for capital projects including new product introductions • Promot e the use of automation to improve productivity, operational efficiency and compliance • Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed Organizational Capability • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products. • Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines. • Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement • Demonstrated ability to influence peers and business partners • Good written and verbal communication skills for both technical and non-technical audiences • Knowledge of GMP, regulatory requirements, computer system validation Basic Requirements • Minimum B.S. in Engineering and experience in Automation Engineering , preferably in major pharmaceutical manufacturing. • 5 + years working experience in Biopharma engineering, operations, or manufacturing. • Qualified applicants must be authorized to work in the United States on a full-time basis.

The Engineer - Automation Engineering will work as a member of the Automation Engineering Department at Eli Lilly, Foundry.