Information Technology Jobs in Campbell, CA

664 positions found — Page 10

Senior Corporate Paralegal
✦ New
Salary not disclosed

Senior Legal Assistant / Corporate Legal Specialist (On‐Site)

Location: San Jose, CA (5 days on‐site)

Compensation: $180K–$200K base + 10% bonus + Equity

A growing, fast‐paced legal department is hiring a Senior Legal Assistant / Corporate Legal Specialist to support the General Counsel of a large, well‐established company. This is a newly created, full‐time role designed for a seasoned legal professional who thrives in a dynamic environment and can anticipate needs before they arise.

About the Role

This position provides high‐level legal, paralegal, and administrative support directly to the GC and broader legal team. The ideal candidate brings a blend of corporate legal experience, including time in both private practice and in‐house, with strong paralegal fundamentals. You'll handle a mix of:

  • Corporate governance support
  • Contract/document management
  • Legal operations support
  • Vendor/matter management
  • Board and entity documentation
  • Signature and workflow coordination
  • Legal technology and CLM systems
  • Day‐to‐day legal team administrative operations

Who They're Looking For

The GC needs someone who is:

  • Experienced: 10+ years supporting corporate legal functions
  • Paralegal‐savvy: Paralegal background strongly preferred
  • Mature and proactive: Can anticipate needs, pivot quickly, and manage shifting priorities
  • Resilient and flexible: Comfortable supporting a GC with a flexible schedule
  • Reliable: Willing to occasionally take calls or respond after hours/weekends
  • Detail‐oriented: Strong command of legal jargon, document management, and corporate governance
  • Tech‐comfortable: Familiar with CLM tools, e‐signature platforms, MS Office, SharePoint, etc.

Industry experience is a nice‐to‐have but not required.

Work Environment

  • Fully on‐site, 5 days per week (some flexibility on an as‐needed basis)
  • Fast‐paced legal department with high visibility to leadership
  • Direct partnership with the GC
  • Collaborative environment with opportunities to streamline processes and support key legal functions
Not Specified
Physician / Psychiatry / California / Locum Tenens / Psychiatry Locums Job Child & Adolescent and Adult Outpatient Coverage in the Bay Area Job
✦ New
Salary not disclosed
San Jose, California 1 day ago

Psychiatry Locums Job Child & Adolescent and Adult Outpatient Coverage in the Bay Area

Details/Requirements: Need is for child & adolescent and adult in-person outpatient coverage for 8-12 hours a week (prefer 8, if possible) starting ASAP x ongoing. Approximately 25% of patients are child & adolescents, ages 5-17 and approx. 75% are adults. Serve patients with developmental disabilities, with a co-occurring mental health diagnosis as well. Strongly prefer child trained Psychiatrists who will also see adults, but may consider an adult Psychiatrist who has extensive experience treating children ages 5 and up. Bilingual in Spanish would be a plus but is not required. Hours: 9am-4:30pm or 5pm, Monday through Friday No call. Initial psychiatric evaluations are 90 minutes for children with 45 minute follow ups. Adult psychiatric evaluations are 60 minutes with 30-45 minute follow ups. Electronic health records, Avatar, so candidates must be technologically savvy to check email, navigate a smart phone, and be able to learn electronic health record. Takes approximately 4 weeks for credentialing. Six month minimum assignments preferred, but the longer the better.

Jackson and Coker offers:+ Weekly Direct Deposit+ Top Rated Malpractice Insurance+ In-House Travel Agency+ 24/7 Recruiter Availability+ Experienced In-House Privileging CoordinatorsExperience why Jackson and Coker has been recognized by Forbes and Staffing Industry Analysts for our commitment to service excellence.Apply Today!

Alex Bloodworth

For more jobs, visit Jackson and Coker .

Not Specified
Litigation Partner or Group (Commercial, Securities, Class Actions, White Collar & Regulatory Attorneys) for Fast-Growing AmLaw Firm
✦ New
Salary not disclosed
San Jose, CA 5 hours ago

Litigation Partner / Group

Commercial • Securities • Class Actions • White Collar • Regulatory

Fast-Growing AmLaw Firm | Nationwide Platform

We are representing a fast-growing AmLaw firm actively building a national litigation platform across complex commercial disputes, securities litigation, class actions, government investigations, and trial work. The firm is making significant strategic investments in lateral partners and groups who want stronger economics, deeper institutional support, and a platform designed to scale high-stakes litigation practices.

This is an opportunity for trial-tested rainmakers who want more than a department — it is built for partners who want cross-selling, premium clients, and a firm that actively invests in their success.

The Platform

The firm represents Fortune 500 companies, financial institutions, private equity sponsors, asset managers, technology companies, and regulated businesses in some of the most complex and high-exposure matters in the market. Litigation partners operate inside a fully integrated platform that includes corporate, securities, regulatory, IP, and employment, allowing clients to manage risk and disputes across their entire enterprise.

The practice supports matters including:

  • Complex commercial and business litigation
  • Securities litigation, shareholder derivative and fiduciary-duty actions
  • Class actions and mass tort defense
  • Antitrust and competition disputes
  • White-collar criminal defense and government investigations
  • Regulatory enforcement (SEC, DOJ, FINRA, CFTC, state AGs)
  • Internal investigations and compliance matters
  • Trade secrets, unfair competition, and business torts
  • Appellate litigation and trial strategy

Who They’re Looking For

The firm is seeking partners — and partner groups — with:

  • A portable book of business
  • Practices in commercial litigation, securities, regulatory, white collar, or class action defense
  • Interest in a platform that delivers real institutional support and cross-practice client expansion

Books typically begin in the mid-six figures and above, with flexibility based on practice mix, clients, and growth potential.

Why Partners Join This Platform

This firm offers:

  • AmLaw-level sophistication with entrepreneurial economics
  • National footprint with flexible office alignment
  • Deep corporate, PE, and regulatory cross-selling
  • Elite trial teams, e-discovery, and litigation support
  • Real marketing and business-development infrastructure
  • Leadership opportunities to shape the litigation platform

Partners move here because they want more leverage, more referrals, and more upside — without BigLaw bureaucracy.

Explore Confidentially

All inquiries are handled in strict confidence.

If you are exploring a platform that offers stronger economics, premium disputes, and real growth support, we welcome a discreet conversation.

Not Specified
Mid-Level Litigation Attorney
✦ New
Salary not disclosed
San Jose, CA 5 hours ago

Litigation Attorney (4+ years of litigation experience) – San Jose and/or Danville

 

Are you a seasoned, personable Litigation Attorney with a robust background looking to gain meaningful experience, build your practice and skillset, and work in a positive, collaborative environment with a firm that continues to experience strong and sustained growth?

 

This is a unique opportunity to step into a well-established, respected firm with a variety of interesting, stable clients. Join a team of devoted, dedicated client advocates who emphasize and appreciate hard work, as well as life ‘outside the office.’

 

We have an outstanding dedicated support staff and we foster a friendly, collegial environment. We offer flexible autonomy regarding hybrid/remote work and scheduling, along with competitive compensation packages and benefits.

 

Primary Responsibilities Include:

·      High level legal analysis

·      Client communication and interaction

·      Depositions

·      Mediations

·      Discovery

·      Document review and analysis

·      Law & Motion practice in state and federal court

·      Legal research and writing

·      Trials and arbitrations as second chair, with first chair opportunities

 

Minimum Qualifications: 

·      Juris Doctorate degree from an ABA-accredited law school

·      Admitted to practice and in good standing with the State Bar of California

·      4+ years of Litigation experience required

·      Motivated, proactive, respectful, friendly, ambitious

·      Must be able to work in our San Jose and/or Danville office 2-3 days per week

·      California resident

 

Benefits Summary:

·      Competitive salary commensurate with experience. Salary range is: $145,000 - $195,000

·      Medical, dental, vision, life insurance, long-term disability insurance, short-term disability insurance

·      401(k) and Profit Sharing Plan with employer contribution

·      CLE, bar dues, and professional development support

 

Strategy Law Core Values:

·      Personal Accountability

·      Respect – No Jerks

·      Integrity

·      Team-Oriented 

·      Achievement

·      Autonomy

·      Collaboration

·      Work/Family/Fun/Balance

 

Strategy Law was formed on the premise that each client’s goals and needs are unique and legal advice should be personalized, exceptional and comprehensive. Our attorneys represent small to medium sized businesses, individuals, growth technology companies, financial institutions, commercial real estate investors and developers, and international companies doing business in the U.S. We take a client-centered, holistic approach to providing legal services and have built our practice as such. Our attorneys are experienced professionals who provide sound legal guidance to complement business strategy and take time to understand each client’s unique needs and goals.

 

Strategy Law Core Focus: Excellent Solutions, Trusted Relationships, Building Community 

 

If you are interested in joining our team, please submit a resume and cover letter stating your salary requirements and why you think you would be a good fit for this position to We encourage candidates with diverse work histories—including those returning to work after a break—to apply.

NO RECRUITERS

Not Specified
REMOTE Senior Associate Attorney
✦ New
Salary not disclosed
San Jose, CA, Remote 5 hours ago

Senior Associate Attorney 


Clarkson has been certified as a Great Place to Work® for 2025 to 2026! 



Job Summary 


We are seeking a skilled, motivated, and ambitious Senior Associate with a passion for mission-driven work, to join our dynamic legal team, specializing in complex consumer class actions. The Senior Associate will be responsible for managing a caseload involving complex legal issues surrounding emerging technology, AI, data privacy and misuse, as well as other complex consumer class actions. Candidates must possess excellent writing skills, with the ability to draft clear, persuasive, and well-structured briefs, motions, and memoranda that require minimal editing, as well as the ability to independently take depositions, present oral arguments, and argue motionsThe ideal candidate will have substantial experience handling key dispositive motions, including motions for summary judgment and motions for class certification, and the ability to independently manage major phases of class action litigationThis is an opportunity to be mentored by industry thought leaders, to creatively pursue interesting cases, and to champion causes that meaningfully impact ordinary people’s lives and the world. 

Essential Duties and Responsibilities 


· Evaluating new cases; preparing and reviewing case proposals 


· Conducting legal research 


· Developing and recommending case strategy 


· Drafting motions and briefs in file-ready form 


· Overseeing filing process for motions and briefs 


· Preparing, finalizing, and serving stipulations, discovery letters, joint statements, and proposed orders 


· Corresponding with co-counsel, opposing counsel, court personnel, and clients as necessary 


· Drafting, propounding, reviewing, and responding to discovery; managing discovery disputes 


· Preparing for and taking/defending depositions 


· Attending mediations, arbitrations, and court hearings 


· Taking argument at mediation, arbitration, and court hearings 


· Attending and/or leading team and firm meetings 


· Adhering to all deadlines (internal and court mandated) 


· Administrative duties as they relate to the practice of law 


Qualifications To perform this job successfully, an individual must be able to perform each essential duty. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 


 


Education and/or Experience 


· 5+ years of Litigation Experience 


· CA Bar Admission Required.  


· Proficiency in Microsoft Office required 


· CA bar exam if licensed in other states 


Skills and Abilities 


· Strong writing, legal research, and analytical skills 


· Proactive thinker, self-sufficient 


· Strong leadership, team management, and organizational skills 


· Strong oral advocacy and negotiation skills 


· Ability to handle a wide variety of legal matters 


· Adherence to all deadlines 


· Effective time management 


· Committed to superior client service 


· Familiarity with e-filing preferred 


Remote working/work at home options are available for this role.
Not Specified
Head of Operations and Manufacturing
Salary not disclosed
Sunnyvale, CA 4 days ago

Head of Operations and Manufacturing Ripple Medical | California (Hybrid or Remote) | Full-Time


ABOUT RIPPLE MEDICAL

Ripple Medical is a health tech company on a mission to revolutionize hypertension management with our cuffless blood pressure wearable. Once cleared by FDA, our product will enable patients to easily and accurately monitor blood pressure at home, empowering them and their providers with actionable data to improve outcomes. We're a collaborative, mission-driven team of 33 working in a medical device regulatory environment to bring this technology to the millions of patients who can benefit.


POSITION SUMMARY

The Head of Operations and Manufacturing will own the end-to-end operational infrastructure required to bring Ripple's FDA-regulated cuffless blood pressure monitor to market and scale production. This is a hands-on leadership role for someone who thrives building from zero to one in a regulated environment: selecting contract manufacturers, standing up supply chains compliant with FDA 21 CFR Part 820, establishing ISO 13485-certified quality management systems, and preparing for direct-to-patient fulfillment.

As a company preparing for 510(k) submission and commercial launch, this role is critical to ensuring we can reliably manufacture and deliver a high-quality, FDA-cleared medical device at scale. The ideal candidate brings deep experience in medical device manufacturing (particularly wearable or electro-optical devices), understands regulated hardware supply chains and design transfer, and can roll up their sleeves while building the team and processes for long-term growth.

This position reports directly to the CEO with high visibility to the leadership team and Board of Directors.


KEY RESPONSIBILITIES

Manufacturing & Production

  • Lead selection and onboarding of contract manufacturing partners with Class II medical device experience, including RFQ, quality audits, contract negotiation, and ongoing management.
  • Own design transfer and manufacturing transfer, working with engineering on DFM principles, Device Master Record (DMR) requirements, and production readiness.
  • Establish production planning, forecasting, and capacity management for V&V builds, pilot production, and volume manufacturing.
  • Drive continuous improvement in yield, quality, and cost while maintaining FDA and ISO compliance.
  • Oversee pilot runs and scale-up, including process validation (IQ/OQ/PQ) and manufacturing controls.

Supply Chain & Procurement

  • Build and manage the end-to-end supply chain, including component sourcing, supplier qualification, and inventory management per FDA purchasing controls.
  • Develop supplier relationships and negotiate terms while ensuring supply continuity, traceability, and risk mitigation.
  • Implement inventory planning to balance working capital with service levels, including buffer strategies for Year 1 launch.
  • Monitor and mitigate supply chain risks: component shortages, single-source dependencies, geopolitical factors, and logistics disruptions.

Quality & Regulatory Compliance

  • Maintain and improve the ISO 13485-certified QMS in partnership with the quality and regulatory team, ensuring FDA 21 CFR Part 820 compliance.
  • Support 510(k) submission activities related to manufacturing, including process validation documentation, DMR development, and device history records (DHR).
  • Define incoming inspection, in-process controls, and final product testing consistent with the risk management file.
  • Manage product certifications for a Class II device, including FDA registration, UDI compliance, and applicable international requirements.
  • Lead root cause analysis and CAPA for quality issues, ensuring post-market surveillance compliance.

Fulfillment & Logistics

  • Design the direct-to-patient fulfillment strategy, including 3PL selection with FDA-cleared Class II device experience.
  • Establish logistics and distribution for nationwide shipping of a regulated device with chain-of-custody and traceability.
  • Develop returns, replacement, and warranty processes that balance patient experience, cost, and compliance.

Team & Organizational Development

  • Start as an individual contributor who executes hands-on, then build and lead the operations team through 510(k) clearance and commercial launch.
  • Establish operational metrics and dashboards for manufacturing, supply chain, and quality performance.
  • Partner with finance on cost modeling, COGS optimization, and operational budgeting.
  • Collaborate cross-functionally with engineering, software, regulatory, and commercial teams.


QUALIFICATIONS

  • 7-12 years in manufacturing, operations, or supply chain, with 3-5+ years in medical devices (Class II preferred), wearables, or regulated hardware.
  • Experience managing contract manufacturers for regulated medical devices, preferably in Asia and/or domestically.
  • Experience at or with CMs/EMS providers (Flex, Jabil, Celestica, Plexus, Sanmina) in Class II medical device or wearable programs is a strong plus.
  • Track record of design transfer and scaling production from pilot to volume for regulated products.
  • ISO 13485 and FDA 21 CFR Part 820 experience required.
  • Familiarity with the 510(k) process and manufacturing documentation (process validations, DMR/DHR) strongly preferred.
  • Bachelor's in Engineering, Supply Chain, Operations, Biomedical Engineering, or related field; MBA or advanced degree a plus.
  • Based in California or travel up to 25%.

COMPENSATION

  • Base Salary: $160,000 - $210,000 USD
  • Performance Bonus: Tied to company milestones and personal objectives
  • Equity: Early-stage stock option grant with meaningful ownership
  • 100% Employer-Paid Healthcare: Medical, dental, and vision
  • Additional Benefits: 401(k) with company match, flexible PTO
Not Specified
Senior Manufacturing Process Engineer
Salary not disclosed
Santa Clara, CA 4 days ago

Senior Manufacturing Process Engineer

Meet has partnered with an exciting Stealth start-up in the Brain-Computer Interface (BCI) space based in the San Francisco Bay area. The company is developing cutting-edge medical devices and technology for the treatment of unmet neurological disorders. The Head of Operations is seeking an experienced Manufacturing Process Engineer to support NPI of electro-mechanical devices in collaboration with suppliers.


This role will focus on hands-on interaction with suppliers to develop manufacturing processes, tooling, and documentation, from design feasability through commercial release. This role will require real-time engagement and technical support of suppliers, and this individual will be expected to travel often to domestic supplier sites and occasionally to international suppliers.


Primary Responsibilities:

  • Serve as the primary technical liaison to external manufacturing partners, ensuring successful delivery of components, assemblies, and finished devices
  • Collaborate with product development teams to ensure designs are manufacturable and compliant with medical device quality system requirements
  • Develop and maintain manufacturing documentation, including work instructions, process flows, and validation protocols
  • Support supplier implementation of specifications, manufacturing processes, and quality requirements
  • Lead and participate in process validation activities including IQ/OQ/PQ, PFMEA, and failure investigations
  • Drive continuous improvement initiatives related to manufacturing efficiency, quality, cost, and scalability
  • Support resolution of non-conformances and corrective actions with suppliers
  • Ensure manufacturing activities comply with applicable regulatory requirements (FDA, ISO 13485, EU MDR, etc.)
  • Provide hands-on technical support to suppliers, including travel as needed (domestic and international)


Role Requirements:

  • B.S. in relevant engineering discipline, or equivalent experience.
  • 10 or more years of medical device manufacturing experience, preferably in senior roles at start-up companies developing and manufacturing electro-mechanical devices.
  • Experience with active implantable systems (Implant, Leads, Externals, etc.).
  • Experience with medical device manufacturing including molding, laser welding, clean room assembly, packaging, labeling, and sterilization.
  • Experience with electronic manufacturing and test including PCB fab, PCA assembly, microelectronics assembly, flip chip, in circuit test (ICT) and functional test.
  • Experience with manufacturing automation.
  • Experience in defining and executing process validation activities.
  • Experience collaborating with internal customers and external partners.
  • Understanding of and experience implementing validating manufacturing processes for medical devices in accordance with FDA and EU Requirements.
  • Experience with Solidworks, Labview / manufacturing process and test automation software.
  • Ability to travel to Domestic and International supplier sites frequently
Not Specified
Director of Manufacturing & Supply Chain
Salary not disclosed
Santa Clara, CA 3 days ago

Company Description

Verdant Robotics' SharpShooter is an advanced precision application system that delivers unparalleled accuracy for weeding, thinning, and other essential crop applications. Designed to seamlessly integrate with existing agricultural practices, this technology ensures precise applications to crops and weeds of varying sizes without sacrificing efficiency. The SharpShooter enhances agricultural processes by reducing labor costs, minimizing chemical usage, and increasing crop yields, making it a trusted choice for leading specialty growers in the U.S., including conventional, organic, and no-till systems. Learn more at Description

We are hiring a hands-on Director of Supply Chain & Production to build and scale our end-to-end supply chain and manufacturing operations. This leader will own production execution—ensuring builds happen on schedule, materials arrive when needed, and customer and investor milestones are met without surprises.

You will drive disciplined production planning, enforce accountability across suppliers and internal teams, and remove blockers before they impact timelines. In a startup environment where resources are tight and priorities shift, you bring structure without slowing momentum. Execution matters here—meeting build schedules, delivering units on time, and scaling cleanly from prototype through volume production.

Our core technology empowers farmers to grow more profitable food. We use computer vision and artificial intelligence to understand every part of every plant at a massive scale -- and with automated robotics, we close the loop and act on that information in real-time. Together with our partners, we are building environmentally-friendly, sustainable, and highly productive farms.


We’re a technology company focused on delivering great customer service, an amazing product, and experience. We’re looking for can-do, roll up the sleeves Director strong on building culture.


Core Responsibilities

  • Own the full supply chain lifecycle: sourcing, procurement, supplier development, planning, logistics, and cost control
  • Lead production ramp from pilot builds to scalable manufacturing (internal and/or contract manufacturers)
  • Own supplier quality and incoming inspection systems
  • Define and execute contract manufacturing strategy
  • Establish spare parts and field service supply architecture
  • Partner with Finance to optimize working capital and inventory efficiency
  • Lead make-vs-buy and capital equipment investment decisions
  • Establish and manage production schedules aligned to company milestones + report out weekly to teams and Executive team; including Board of Directors.
  • Negotiate and manage strategic supplier contracts (electronics, mechanical systems, long-lead components, capital equipment)
  • Drive BOM cost reduction and margin improvement initiatives
  • Implement production KPIs: throughput, yield, on-time delivery, inventory turns, and cost
  • Identify supply risks early (capacity, geopolitical exposure, sole-source dependencies) and implement mitigation strategies
  • Partner closely with Engineering on NPI, DFM, supplier qualification, and design-to-cost efforts
  • Develop S&OP and demand planning processes appropriate for a scaling startup
  • Stand up scalable systems (ERP/MRP, forecasting, reporting infrastructure)
  • Recruit, develop, and lead a lean, high-performing supply chain and production team
  • Develop operational processes for parts inventory, ordering, and supporting a dealer network.
  • A focus on managing budget and forecast.


What Success Looks Like (First 12-18 Months)

  • Production ramps cleanly to meet customer and board-level milestones
  • Clear visibility into supply risk, cost structure, and capacity constraints; identify alternate solutions.
  • Critical supplier contracts secured with favorable commercial and operational terms
  • Improved production yield, cycle time, and on-time delivery
  • Build processes to support a dealer network.
  • A resilient supply base capable of supporting rapid growth
  • A strong, accountable team in place that executes without constant oversight


Qualifications

  • A bachelor’s degree in engineering, supply chain management, operations, or a related field is required; an advanced degree is a plus.
  • 10+ years of leadership experience in supply chain and/or production within EV, autonomy, robotics, automotive, or other complex hardware environments
  • Proven experience scaling from NPI/prototype to volume manufacturing
  • Demonstrated success negotiating multi-million-dollar supplier agreements
  • Strong production execution background with a track record of delivering against aggressive timelines
  • Experienced team builder who attracts, develops, and retains high-performing talent
  • Comfortable operating in ambiguity and building systems from scratch
  • Technical fluency to engage deeply with engineering and manufacturing teams
  • Experience in a startup or VC-backed growth environment preferred
  • Bias toward action and ownership; solves problems early and decisively
  • Expertise in Production Planning and Manufacturing Operations.
  • Proficiency in Supply Chain Management and inventory optimization techniques.
  • Experience implementing process improvements, cost-reduction strategies, and maintaining quality standards in manufacturing.
  • Experience in the agricultural technology sector or similar industries is preferred.


Salary Range: $185,000 - $225,000 base + Equity


Verdant reserves the ability to adjust the compensation range based on the final candidate's experience, skillset, and geography. In addition to on-target earnings, we offer equity grants, as every employee should have a stake in the company's growth. If you're above this compensation target, we encourage you to reach out and discuss the entire package and opportunity before deciding not to pursue this position.


Email Resume to

 

Verdant Robotics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, genetics, sexual orientation, gender identity, or gender expression.


Not Specified
Lead PMIC Design Engineer (RTL)
✦ New
🏢 SBT
Salary not disclosed
Sunnyvale, CA 1 day ago

SBT is the exclusive retained recruiting firm for this position.


Company Overview

This confidential startup is a well-funded early-stage semiconductor company focused on advancing AI-driven design to address emerging challenges in the artificial intelligence ecosystem. The company is developing innovative technologies that leverage automation and machine learning to accelerate the design and development of complex analog semiconductor solutions. By applying AI to traditionally manual and time-intensive design processes, the organization aims to unlock faster innovation cycles and enable the next generation of AI hardware infrastructure.


Job Role

  • Design and implement digital control logic for power management ICs
  • Work closely with analog engineering teams to ensure effective integration between digital control blocks and analog power circuitry
  • Develop high-quality, power-efficient RTL using Verilog or SystemVerilog to support key features
  • Contribute to product readiness for manufacturing by supporting design-for-test methodologies
  • Create and execute comprehensive verification strategies, including mixed-signal simulations and behavioral modeling


Qualifications

  • BS or MS degree in Electrical Engineering, Computer Engineering, or a related field.
  • 10+ years of experience in digital IC design, including significant experience developing solutions for mixed-signal or power management semiconductor products.
  • Strong proficiency in RTL development using Verilog or SystemVerilog for synthesizable digital design.
  • Hands-on experience designing digital control logic for power conversion systems, including control loops used in power management or DC-DC converter applications.
Not Specified
Private Equity Associate/Senior Associate
✦ New
Salary not disclosed
San Jose, CA 1 day ago

About the firm:

This San Francisco‑area private equity firm specializes in providing growth capital and structured financing to established, founder‑led tech and technology‑enabled services companies in the U.S., typically investing in lower‑middle‑market businesses that haven’t had prior institutional funding. It partners with business owners by offering capital along with strategic, operational support to help these companies scale, accelerate growth, and become market leaders, while often taking minority stakes and aligning incentives without forcing founders to give up control.


About the role:

  • Deal Sourcing & Screening: Research and identify potential investment opportunities in tech and tech-enabled companies.
  • Financial Analysis & Modeling: Build detailed financial models, perform valuations, and assess potential returns and risks.
  • Due Diligence: Support the evaluation of target companies, including market research, competitive analysis, and operational reviews.
  • Investment Memoranda: Prepare presentations and investment memos for internal committees and decision-makers.
  • Portfolio Support: Assist portfolio companies with growth initiatives, performance tracking, and strategic projects post-investment.
Not Specified
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