Manager, Automation Engineering
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![]() United States, California, Cypress | |
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Boldly innovating to create trusted solutions that detect, predict, and prevent disease. Discover your power to innovate while making a difference in patients' lives.iRhythm is advancing cardiac care...Join Us Now! At iRhythm, we are dedicated, self-motivated, and driven to do the right thing for our patients, clinicians, and coworkers. Our leadership is focused and committed to iRhythm's employees and the mission of the company. We are better together, embrace change and help one another. We are Thinking Bigger and Moving Faster. About This Role iRhythm is seeking a highly experienced and motivated Manager, Automation Engineering with a medical device industry background and minimum 10 years relevant industry experience to join iRhythm's engineering team. This roll is based at the manufacturing site in Cypress, CA and will have responsibility for strategizing and executing all industrial automation projects related to manufacturing production assembly and packaging. The Manager will plan and manage multiple projects with various complexity with the accountability for successful execution of all projects. This position will be key player in developing and scaling process/equipment automation group at the manufacturing site. Our work environment is fast-paced, with a collaborative atmosphere. Most of all, we are passionate about delivering innovations that improve the quality of health care and the patient experience. We are looking for like-minded individuals to join our team today! Responsibilities include: * Analyze manufacturing operations and design sophisticated industrial automation solutions in support of production growth and cost reduction initiatives. * Comprehensive understanding of end-to-end manufacturing processes, including assemblies, secondary packaging, and sub-assembly processes * Previous experience leveraging external automation integrator partners throughout the project phases, from initial selection diligence, design, reviews, buy-off, onsite commissioning. * Solid understanding of the available technologies, industry trends, and ability to select right designs and communicate effectively across organization. * Leads and coordinates cross-functional teams (both internal and external resources) to ensure meeting timely committed milestones. Actively manages cross-functional alignment and drives the resolution of issues. * Manages multiple, concurrent custom automation projects of various complexities (pilot to high-volume) from initiation of the projects to integration of the equipment into manufacturing with a future look towards lifecycle management and sustaining activities. * Understanding of Critical to Quality (CTQ) design elements and cascading CTQs to design robust manufacturing processes and process controls. * Acts as mentor in the engineering organization. Coaches and develops associates across a range of career levels * Project manage complex project and explain complex concepts and strategies in understandable terms across organization. About you: * BS in Engineering or Science; MS and/or MBA degree preferred. * 8+ years of manufacturing and engineering experience in industrial automation. * 8+ years hands-on experience with industrial automation including mechanical (robots, conveyors, etc.), or control system site (such as PLC/DCS design and programing). Solid experience with full integration of the equipment. * 8+ years solid background with developing URS, and all aspects of the equipment design and validation process, including design reviews, pre-FAT, FAT, installation, IQ/OQ, and product process validation (PPQ). * Seasoned project management skills; multiple projects of high complexity and/or large-scale nature. * Strong record of technical achievement designing & successfully commissioning automation equipment solutions. * Experience with technical understanding of design for manufacturability/Assembly/Automation (DFM/DFA), process excellence methodologies including Six-Sigma, Lean, cGMP guidelines. * Experience working in medical device manufacturing environment is highly desirable. * Prefer medical device industry experience with knowledge of cGMP manufacturing. * Strong collaborator and communicator with a high degree of ability to understand business needs. Excellent written, verbal communication and presentation skills. * Experience managing direct report engineers and technicians preferred, but not a must. Ability to develop and upskill other engineers. * Experience working at automation design and integrator companies designing custom automation preferred. * Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities. What's in it for you: This is a regular full-time position with competitive compensation package, excellent benefits including medical, dental, and vision insurances (all of which start on your first day), health savings account employer contributions (when enrolled in high deductible medical plan), cafeteria plan pre-taxed benefits (FSA, dependent care FSA, commute reimbursement accounts), travel reimbursement for medical care, noncontributory basic life insurance & short/ long term disability. Additionally, we offer: * emotional health support for you and your loved ones * legal / financial / identity theft/ pet and child referral assistance * paid parental leave, paid holidays, travel assistance for personal trips and PTO! iRhythm also provides additional benefits including 401(k) (with company match), an Employee Stock Purchase Plan, pet insurance discount, unlimited amount of LinkedIn Learning classes and so much more! FLSA Status: Exempt #LI-JR1 Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location. Estimated Pay Range
$130,600
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$191,700 USD As a part of our core values, we ensure a diverse and inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws. iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at taops@irhythmtech.com About iRhythm Technologies Make iRhythm your path forward. Zio, the heart monitor that changed the game. |