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YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_99efe590-126"},"title":"Senior Clinical Pharmacist","description":"<p>Hims &amp; Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health.</p>\n<p>We are seeking an experienced and driven Senior Clinical Pharmacist to serve as the clinical and operational backbone of our 503A compounding pharmacy.</p>\n<p><strong>About the Role:</strong></p>\n<p>This is a high-impact, cross-functional role that bridges clinical expertise, regulatory compliance, quality improvement, and day-to-day operational leadership.</p>\n<p><strong>You Will:</strong></p>\n<p><strong>Clinical &amp; Regulatory</strong></p>\n<ul>\n<li>Review and implement clinical guideline updates</li>\n<li>Conduct Pharmacy Information Booklet and Medication guide review for all dispensed products</li>\n<li>Perform clinical reviews arising from Medication Errors and identified issues</li>\n<li>Support pharmacy literature reviews and stay current on applicable state and federal pharmacy law</li>\n<li>Obtain state licenses</li>\n</ul>\n<p><strong>Product Launches &amp; Change Management</strong></p>\n<ul>\n<li>Prepare the pharmacy team for new product launches, including guideline changes, Rx/label/packaging expectations, and staff education</li>\n<li>Partner with the fulfillment team to align on collateral requirements and pack-out expectations</li>\n<li>Ensure product pack-out validation and fit tests prior to launch</li>\n<li>Coordinate with IT on improvements including prescription label changes, product name reviews, and sig reviews</li>\n</ul>\n<p><strong>Quality &amp; Continuous Improvement (CQI)</strong></p>\n<ul>\n<li>Lead the CQI program: audit, analyze, and trend pharmacy error and near-miss data</li>\n<li>Facilitate monthly CQI meetings with pharmacist and technician teams; present findings at quarterly leadership meetings</li>\n<li>Drive follow-up and implementation of CQI initiatives and process improvement projects</li>\n<li>Maintain the AZ facility call log and ensure timely resolution and documentation</li>\n</ul>\n<p><strong>Operations &amp; Order Management</strong></p>\n<ul>\n<li>Manage test orders and test labels to validate system changes</li>\n<li>Author, review, and update pharmacy SOPs</li>\n<li>Guide the pharmacy team on protocols during technology failures or system downtime</li>\n</ul>\n<p><strong>Cross-Functional Coordination</strong></p>\n<ul>\n<li>Serve as the primary clinical liaison between pharmacy and teams including inventory, fulfillment, care operations, learning &amp; development, and engineering</li>\n<li>Receive and review provider communications; distill and disperse relevant clinical guidance, updates, and directives to the pharmacy team in a timely and structured manner</li>\n<li>Handle escalated patient communications from CX, including shipping errors and clinical concerns</li>\n</ul>\n<p><strong>Clinical Resource &amp; Communication</strong></p>\n<ul>\n<li>Act as the primary clinical resource for staff pharmacists and technicians</li>\n<li>Prepare slide decks, Google Docs, and Sheets for clinical meetings and patient profile reviews</li>\n</ul>\n<p><strong>You Have:</strong></p>\n<ul>\n<li>Doctor of Pharmacy (PharmD) from an ACPE-accredited program</li>\n<li>Active, unrestricted Registered Pharmacist (RPh) license in Arizona</li>\n<li>2+ years of post-licensure pharmacy experience, with at least 1 year in a supervisory or senior clinical capacity</li>\n<li>Strong cross-functional communication skills; comfortable working with engineering, operations, and clinical teams</li>\n<li>Willingness to obtain non-resident pharmacist licenses and serve as back up PIC when needed</li>\n</ul>\n<p><strong>Our Benefits:</strong></p>\n<ul>\n<li>Competitive salary &amp; equity compensation for full-time roles</li>\n<li>Comprehensive health benefits including medical, dental &amp; vision, and parental leave</li>\n<li>Employee Stock Purchase Program (ESPP)</li>\n<li>Employee discounts on hims &amp; hers online products</li>\n<li>401k benefits with employer matching contribution</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_99efe590-126/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Hims & Hers","sameAs":"https://www.hims.com","logo":"https://logos.yubhub.co/hims.com.png"},"x-apply-url":"https://jobs.ashbyhq.com/hims-and-hers/aa03d4ba-3c40-4880-bb97-5e56fa275623?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"Full time","x-salary-range":null,"x-skills-required":["PharmD","Registered Pharmacist (RPh)","clinical guidelines","regulatory compliance","quality improvement","operational leadership"],"x-skills-preferred":[],"datePosted":"2026-10-26T16:24:56.311Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Gilbert, Arizona"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"PharmD, Registered Pharmacist (RPh), clinical guidelines, regulatory compliance, quality improvement, operational leadership"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_44759c38-818"},"title":"Operations Manager, Compounding (Swing)","description":"<p>Hims &amp; Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health.</p>\n<p>The Operations Manager, Compounding, is a vital role within our organization, reporting directly to the Director of Operations, Non-Sterile Compounding. This position is responsible for leading a team of compounding professionals and overseeing the daily operations of the compounding department.</p>\n<p><strong>You Will:</strong></p>\n<ul>\n<li>Daily Operations Management: Plan, coordinate, and oversee daily production schedules, ensuring timely delivery of compounded products.</li>\n<li>Team Leadership: Lead and supervise a team of lab managers, pharmacy tech leads, and pharmacy technicians.</li>\n<li>Process Optimization: Continuously evaluate existing compounding processes and identify opportunities for improvement.</li>\n<li>KPI Tracking &amp; Reporting: Monitor key performance indicators (KPIs) related to safety, quality, and productivity.</li>\n<li>Safety &amp; Compliance: Ensure that all compounding activities comply with USP, FDA, OSHA, and other relevant regulations.</li>\n<li>Inventory &amp; Material Handling: Oversee inventory management, ensuring adequate stock levels of compounding materials and proper handling and storage of hazardous and non-hazardous substances.</li>\n<li>Collaboration &amp; Problem Solving: Work closely with cross-functional teams to address operational challenges and drive production efficiency.</li>\n</ul>\n<p><strong>You Have:</strong></p>\n<ul>\n<li>Experience: 5-7+ years of hands-on experience in pharmaceutical compounding, manufacturing, fulfillment, or a related operational environment.</li>\n<li>Education: Bachelor’s degree in a relevant field (e.g., Pharmacy, Chemistry, Engineering) is preferred but not required.</li>\n<li>Technical Skills: Proficiency in warehouse management systems (WMS) and operational reporting tools.</li>\n<li>Soft Skills: Excellent communication, leadership, and problem-solving skills.</li>\n</ul>\n<p><strong>Our Benefits:</strong></p>\n<ul>\n<li>Competitive salary &amp; equity compensation for full-time roles</li>\n<li>Unlimited PTO, company holidays, and quarterly mental health days</li>\n<li>Comprehensive health benefits including medical, dental &amp; vision, and parental leave</li>\n<li>Employee Stock Purchase Program (ESPP)</li>\n<li>401k benefits with employer matching contribution</li>\n<li>Offsite team retreats</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_44759c38-818/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Hims & Hers","sameAs":"http://hims.com","logo":"https://logos.yubhub.co/hims.com.png"},"x-apply-url":"https://jobs.ashbyhq.com/hims-and-hers/99776387-4304-49d1-a4d1-6fc21238c59d?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"Full time","x-salary-range":null,"x-skills-required":["pharmaceutical compounding","leadership","process optimization","safety and compliance","inventory management"],"x-skills-preferred":["sterile and non-sterile compounding","hazardous and non-hazardous materials","regulatory compliance","continuous improvement"],"datePosted":"2026-10-25T09:41:31.950Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Gilbert, Arizona"}},"employmentType":"FULL_TIME","occupationalCategory":"Operations","industry":"Healthcare","skills":"pharmaceutical compounding, leadership, process optimization, safety and compliance, inventory management, sterile and non-sterile compounding, hazardous and non-hazardous materials, regulatory compliance, continuous improvement"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_65aec170-ecd"},"title":"Compliance Systems Specialist","description":"<p>Hims &amp; Hers is seeking a Compliance Systems Specialist to own the setup and day-to-day operation of their compounding compliance software.</p>\n<p>The successful candidate will configure the system to document and track everything required by USP &lt;795&gt;, &lt;797&gt;, and &lt;800&gt;, train the compounding team, and report on compliance to pharmacy leadership.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Configure compliance software to meet USP &lt;795&gt;, &lt;797&gt;, and &lt;800&gt; requirements</li>\n<li>Generate reports to demonstrate compliance</li>\n<li>Train compounding staff on software usage</li>\n<li>Run daily and monthly compliance reports</li>\n<li>Troubleshoot system issues and answer staff questions</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>3+ years of compounding experience</li>\n<li>Strong knowledge of USP &lt;795&gt;, &lt;797&gt;, and &lt;800&gt;</li>\n<li>Current registration as a Certified/Registered Pharmacy Technician</li>\n<li>Experience teaching or training others</li>\n<li>Analytical and troubleshooting skills</li>\n<li>Clear written and verbal communication</li>\n</ul>\n<p>Preferred Qualifications:</p>\n<ul>\n<li>Certified Compounded Sterile Preparation Technician (CSPT) or Certified Non-Sterile Compounding Technician</li>\n<li>Prior experience implementing compliance software</li>\n<li>Flexibility to work weekends or off hours</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Competitive pay</li>\n<li>Potential equity compensation</li>\n<li>ESPP Plan</li>\n<li>Flexible PTO</li>\n<li>Holidays observances</li>\n<li>Quarterly Mental Health Days</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_65aec170-ecd/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Hims & Hers","sameAs":"https://hims.com/","logo":"https://logos.yubhub.co/hims.com.png"},"x-apply-url":"https://jobs.ashbyhq.com/hims-and-hers/5b699ebe-ebf5-45bc-82bc-36e19393eae4?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"Full time","x-salary-range":null,"x-skills-required":["USP <795>","USP <797>","USP <800>","compliance software","training","analytical skills"],"x-skills-preferred":["Certified Compounded Sterile Preparation Technician (CSPT)","Certified Non-Sterile Compounding Technician","compliance software implementation"],"datePosted":"2026-10-24T23:46:16.705Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Gilbert, Arizona, AZ"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"USP <795>, USP <797>, USP <800>, compliance software, training, analytical skills, Certified Compounded Sterile Preparation Technician (CSPT), Certified Non-Sterile Compounding Technician, compliance software implementation"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_dc53f5cd-f48"},"title":"Quality Control Specialist","description":"<p>Hims &amp; Hers is seeking a highly motivated Quality Control Specialist to support and report to the Senior Manager Quality Operations. The successful candidate will be responsible for inspecting and testing products before, during, and after the manufacturing process to ensure compliance with company and regulatory standards.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Perform in-process and post-production quality checks, including testing and dispositioning products.</li>\n<li>Provide reports and trending data to QA management.</li>\n<li>Support external manufacturer non-conformance investigations.</li>\n<li>Manage product retains and inspections.</li>\n<li>Document and review records, including SOP generation and batch record review.</li>\n<li>Detect training needs and provide reports to Site Manager.</li>\n<li>Assist with incoming raw material inspections.</li>\n<li>Assist with drafting SOPs and protocols.</li>\n<li>Ensure compliance with USP &lt;795&gt; and cGMP cleaning standards.</li>\n<li>Assist in audit activities.</li>\n<li>Assist with the management and reporting of samples to be tested with contract laboratories.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>B.S. in chemistry, biology, quality management, engineering, or related discipline preferred.</li>\n<li>2+ years experience in quality assurance/control, process engineering, and/or product formulation.</li>\n<li>Experience within a 503b outsourcing facility.</li>\n<li>Aseptic processing experience and knowledge of ISO 14644.</li>\n<li>Working knowledge of USP-NF standards &lt;795&gt;, &lt;797&gt;, &lt;800&gt;.</li>\n<li>Experience in cGMP or regulated environment with knowledge of FDA 21, CFR 210, and 211.</li>\n<li>Excellent interpersonal and communication skills.</li>\n<li>Solid understanding of product testing and best practices.</li>\n<li>Ability to multi-task and work independently.</li>\n<li>Highly motivated self-starter with solid computer skills.</li>\n<li>Working knowledge and application of statistical analysis.</li>\n<li>Knowledge and experience in technical writing and auditing.</li>\n</ul>\n<p><strong>Benefits:</strong></p>\n<ul>\n<li>Competitive pay with equity compensation.</li>\n<li>ESPP Plan.</li>\n<li>Flexible PTO.</li>\n<li>Holidays observances.</li>\n<li>Quarterly Mental Health Days.</li>\n<li>High-coverage medical, dental &amp; vision.</li>\n<li>Pet Insurance.</li>\n<li>One Medical Membership.</li>\n<li>Disability Benefits.</li>\n<li>Employee Assistance Program.</li>\n<li>Life and AD&amp;D Benefits.</li>\n<li>Fitness stipend.</li>\n<li>Backup childcare.</li>\n<li>Family forming resources.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_dc53f5cd-f48/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Hims & Hers","sameAs":"https://www.hims.com","logo":"https://logos.yubhub.co/hims.com.png"},"x-apply-url":"https://jobs.ashbyhq.com/hims-and-hers/645f2ad7-d656-4d31-818f-5fec30ccfbc7?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"Full time","x-salary-range":null,"x-skills-required":["quality assurance","process engineering","product formulation","cGMP","USP <795>","ISO 14644","statistical analysis","technical writing","auditing"],"x-skills-preferred":["aseptic processing","regulated environment","FDA 21, CFR 210, and 211"],"datePosted":"2026-10-24T21:35:08.466Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Gilbert, Arizona"}},"employmentType":"FULL_TIME","occupationalCategory":"Operations","industry":"Healthcare","skills":"quality assurance, process engineering, product formulation, cGMP, USP <795>, ISO 14644, statistical analysis, technical writing, auditing, aseptic processing, regulated environment, FDA 21, CFR 210, and 211"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9a363576-691"},"title":"Quality Systems Document Control Specialist","description":"<p>Hims &amp; Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health.</p>\n<p>We are looking for a Quality Systems Document Control Specialist to join our Quality Unit in XeCare Pharmacy. This role is responsible for supporting the document control system and lifecycle of controlled documents in a compounding pharmacy operating under 503A regulations.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Support the administration of the Document Control System, ensuring proper management of controlled documents such as SOPs, batch records, logbooks, forms, policies, and protocols.</li>\n<li>Support the site level implementation of change controls and the impact to site documentation and defined processes.</li>\n<li>Support the design and enhancement of quality system tools and workflows, ensuring alignment with regulatory requirements and business needs.</li>\n<li>Issue and track SOPs and other controlled documents, ensuring only current, approved versions are in circulation.</li>\n<li>Assist in drafting, editing, and formatting SOPs, work instructions, and policies, ensuring clarity, consistency, and alignment with USP &lt;795&gt;, &lt;797&gt;, &lt;800&gt;, and FDA 21 CFR 210/211.</li>\n<li>Support SOP lifecycle management, including periodic review, approval workflows, revision history tracking, and retirement of obsolete versions.</li>\n<li>Support cross-functional SME reviews of SOPs and controlled documents, ensuring input from QA, Production, QC, and Compliance.</li>\n<li>Ensure timely training roll-out when new or revised SOPs are released, and maintain records to demonstrate compliance in alignment with the Training department and Operations teams.</li>\n<li>Maintain both electronic and physical filing systems, ensuring secure storage, easy retrieval, and audit readiness.</li>\n<li>Monitor document-related deviations, including missing signatures, uncontrolled copies, or outdated references, and escalate to QA Management for corrective action.</li>\n<li>Prepare and provide documentation packages for regulatory inspections and customer audits.</li>\n<li>Partner with QS Management to support continuous improvement of the document control process, including digitization initiatives and standardization projects.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Bachelor’s degree preferred in a relevant discipline (science, quality, or engineering-related field) or equivalent combination of education and experience.</li>\n<li>3+ years of related experience in quality, manufacturing, or a regulated industry may substitute for a degree.</li>\n<li>Hands-on experience with SOP drafting, formatting, and controlled documentation systems.</li>\n<li>In-depth knowledge of cGMP documentation practices, USP standards, and FDA record-keeping requirements.</li>\n<li>Exceptional attention to detail with strong editing, writing, and organizational skills.</li>\n<li>Familiarity with electronic document management systems (EDMS) or validated document control or quality management software.</li>\n<li>Strong collaboration skills, with the ability to work across QA, Production, and Compliance teams.</li>\n</ul>\n<p><strong>Benefits:</strong></p>\n<ul>\n<li>Comprehensive health benefits including medical, dental &amp; vision, and parental leave</li>\n<li>401k benefits with employer matching contribution</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_9a363576-691/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Hims & Hers","sameAs":"https://www.hims.com","logo":"https://logos.yubhub.co/hims.com.png"},"x-apply-url":"https://jobs.ashbyhq.com/hims-and-hers/056755b5-5359-4970-9731-3a82243164a4?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"onsite","x-experience-level":null,"x-job-type":"Full time","x-salary-range":null,"x-skills-required":["SOP drafting","controlled documentation systems","cGMP documentation practices","USP standards","FDA record-keeping requirements","electronic document management systems (EDMS)","quality management software"],"x-skills-preferred":[],"datePosted":"2026-10-24T19:03:59.249Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Gilbert, Arizona; Mesa, Arizona"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"SOP drafting, controlled documentation systems, cGMP documentation practices, USP standards, FDA record-keeping requirements, electronic document management systems (EDMS), quality management software"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_4d45bdc6-dc3"},"title":"Area Manager - Facilities Maintanence","description":"<p>Hims &amp; Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health.</p>\n<p>This role reports to the Director of Industrial Engineering. The Area Manager, Maintenance Facilities provides mid-level support to the Operations, Engineering &amp; Maintenance Department by applying predictive and preventive maintenance procedures for all critical production equipment in the warehouse like HVAC, Compressor, Forklifts etc.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Equipment Maintenance – Assist with or perform independently corrective, preventive and planned maintenance activities on production-related equipment such as conveyance, shelving, racking etc., powered industrial trucks, and building equipment such as HVAC, Air compressors, water filtration as needed.</li>\n<li>Building Maintenance – Perform painting, sheetrock repairs, and general tenant improvement work as needed. Perform minor repairs on doors, dock plates, and plumbing to resolve problems and ensure successful operation. Evaluate, repair and maintain plumbing, electrical and HVAC systems.</li>\n<li>Facility Cleanliness / Safety – Ensure the primary work areas are organized, neat and clean both during and upon completion of maintenance related activities. Adhere to 5S principles. Identify and act immediately regarding any safety hazards, spills, etc., to avoid the risk of accidents. Use safe lifting techniques and operate power equipment in a safe manner. Abide by all stated regulations while performing work. Understands and complies with all hazardous energy policies and procedures including lock-out/tag-out.</li>\n<li>Fabrication – Utilize materials and tools to assist with the creation of custom equipment to support the operation (i.e., wood, metal, etc.).</li>\n<li>Record Keeping -- Perform necessary data entry (i.e., work order tracking/filing) and keep current tools and documents updated as necessary (i.e., Safety Data Sheets). Maintain records using appropriate software (i.e. Maintenance Connection) to ensure accountability of time, parts and repairs.</li>\n<li>Identify facilities issues and develop an ongoing strategy to chart trends and take appropriate remedial action from a predictive maintenance approach.</li>\n<li>Communicate to management all issues that could result in safety risks or those that might cause loss to Hims or its associates.</li>\n<li>Work as directed in all areas of the Warehouse to maintain safety and health standards for the facility.</li>\n<li>Perform calibration and testing procedures on equipment to ensure accurate operation and compliance with quality standards.</li>\n<li>Respond promptly to equipment breakdowns, emergencies, and production interruptions to minimize downtime.</li>\n<li>Work closely with production personnel to coordinate repairs and minimize disruptions to the manufacturing process.</li>\n<li>Identify opportunities for process optimization, efficiency improvements, and cost savings related to equipment maintenance and operation.</li>\n<li>Participate in cross-functional teams to implement improvement projects and contribute to the continuous improvement culture within the organization.</li>\n<li>Stay updated with industry trends, technological advancements, and best practices related to general equipment maintenance.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>5+ years of experience in maintenance, facilities, or field with related skills.</li>\n<li>3+ years of formal leadership experience with direct reports</li>\n<li>Ability to safely lift and carry items weighing up to 50 pounds, either in conjunction with his or her regular responsibilities or those assigned in other areas as directed.</li>\n<li>Use of business computer systems and applications,specifically, Microsoft Word, Excel, and Project Management</li>\n<li>Ability to troubleshoot problems with machinery without supervision or direction.</li>\n<li>Ability to document predictive/preventive maintenance charts, technical data and other data; interpret data and provide relevant input for process improvement.</li>\n<li>Ability to communicate effectively with others using spoken and written English (Bilingual in Spanish preferred)</li>\n<li>Ability to bend, stoop, reach overhead with arms and hands and climb ladders; must be able to climb stairs up to three flights and not be afraid of heights utilizing scissor or bucket lifts.</li>\n<li>Ability to work cooperatively and collaboratively with others; conducts working relationships in a manner acceptable to others and to the organization.</li>\n<li>Demonstrated high level ability to troubleshoot, maintain, and operate advance technical equipment in a related industry.</li>\n<li>Demonstrated ability to teach and motivate in a highly technical and fast paced environment</li>\n<li>Have knowledge of and experience with PLC systems</li>\n<li>Have knowledge of and experience with CMMS systems</li>\n<li>Have formal training or certification through an accredited institution in at least one of the following areas: electrical, mechanical, plumbing, air compression, PLC system or HVAC trades</li>\n<li>Must be at least 18 years of age and present state-required proof of age documents.</li>\n<li>High school diploma or equivalent GED required.</li>\n</ul>\n<p><strong>Benefits:</strong></p>\n<ul>\n<li>Competitive salary &amp; 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They work on intricate tasks such as chip architecture, circuit design, and verification to ensure the efficiency and reliability of semiconductor products. These engineers play a crucial role in advancing technology and enabling innovations in various industries.</p>\n<p>You have spent the last few years deep in RTL code, turning specifications into working digital logic that actually synthesizes and meets timing. Good design is not just about functionality for you. It is about creating clean, robust RTL that enables efficient verification and predictable implementation.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Write and review Verilog, SystemVerilog, or VHDL RTL for block-level designs including state machines, pipelines, FIFOs, and memory controllers based on micro-architecture specifications</li>\n<li>Run RTL quality checks using tools like linting, CDC/RDC analysis, and synthesis to ensure your design is clean before handoff to physical design</li>\n<li>Collaborate with verification engineers to debug testbench failures, refine corner cases, and close coverage gaps</li>\n<li>Work with physical design teams to resolve timing issues, optimize logic for synthesis, and support timing closure from netlist through signoff</li>\n<li>Implement standard interface protocols including AXI, APB, AHB, I2C, and SPI within SoC subsystems</li>\n<li>Use scripting in Python, Tcl, or shell to automate repetitive tasks in the design flow and improve team productivity</li>\n<li>Participate in design reviews with cross-functional teams across the globe, clearly communicating design decisions and tradeoffs</li>\n</ul>\n<p><strong>The Impact You Will Have</strong></p>\n<ul>\n<li>Contribute RTL blocks that achieve timing, area, and power targets while minimizing design iterations</li>\n<li>Deliver full SoC designs that ship in products for automotive, aerospace, defense, and high-performance computing customers</li>\n<li>Improve design quality and reduce downstream debug time by catching issues early through disciplined use of lint, CDC, and synthesis checks</li>\n<li>Enable faster project ramp by writing clear design documentation and participating in knowledge transfer across global teams</li>\n<li>Help refine internal design flows and methodologies by identifying bottlenecks and proposing automation or process improvements</li>\n<li>Support customer-specific design requirements by translating high-level specs into implementable RTL that meets project constraints</li>\n<li>Build reusable IP blocks and design patterns that accelerate future projects across the Solutions group</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Bachelor&#39;s or Master&#39;s degree in Electrical Engineering or Computer Engineering</li>\n<li>3 to 4 years of hands-on experience in ASIC or FPGA RTL design, implementation, and debug</li>\n<li>Strong proficiency in Verilog, SystemVerilog, or VHDL RTL coding for registers, pipelines, state machines, memories, and FIFOs</li>\n<li>Working knowledge of the ASIC design flow from micro-architecture through RTL development, synthesis, and timing closure</li>\n<li>Experience using industry-standard tools such as simulators, lint checkers, CDC/RDC analysis tools, synthesis tools, and static timing analysis is preferred</li>\n<li>An understanding of standard interface protocols including AXI, APB, AHB, I2C, and SPI is preferred</li>\n</ul>\n<p><strong>Benefits</strong></p>\n<ul>\n<li>Comprehensive medical and healthcare plans that work for you and your family</li>\n<li>In addition to company holidays, we have ETO and FTO Programs</li>\n<li>Maternity and paternity leave, parenting resources, adoption and surrogacy assistance, and more</li>\n<li>Purchase Synopsys common stock at a 15% discount, with a 24-month look-back</li>\n<li>Save for your future with our retirement plans that vary by region and country</li>\n<li>Competitive salaries</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a 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tools"],"datePosted":"2026-10-08T05:03:50.463Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Gilbert, Arizona"}},"occupationalCategory":"Engineering","industry":"Technology","skills":"ASIC or FPGA RTL design, Verilog, SystemVerilog, VHDL, RTL coding, ASIC design flow, linting, CDC/RDC analysis, synthesis, Python, Tcl, shell scripting, AXI, APB, AHB, I2C, SPI, PCIe, DDR, Ethernet, SystemVerilog assertions, C++, low-power design methodologies, UPF, DFT requirements, Git-based development flows, formal verification tools, AI-assisted engineering tools","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":98000,"maxValue":147000,"unitText":"YEAR"}}}]}