Jobs in San Mateo County, CA

666 positions found — Page 24

Trusts & Estates Litigation Attorney: Oakland, CA
Salary not disclosed

We are working with highly respected, growing, full-service, Oakland, California based law firm with a strong commitment to providing exceptional legal services to its clients. The firm seeks a highly motivated and experienced Trust & Estates Litigation Attorney to join its Trusts and Estates Litigation Practice Group, representing a diverse client base including high-net-worth individuals, fiduciaries, and charitable organizations, in all aspects of trust and estate controversies.

The ideal candidate will have five or more (5+) years of dedicated experience in trust, estate, and conservatorship litigation in California. The role offers the successful candidate the opportunity to manage a diverse caseload, work closely with partners, and take a lead role in all phases of litigation, from initial case assessment through trial and appeal. Minimum billable hours are 1610/yr. Attorneys meeting or exceeding that goal may increase their earnings significantly through the firm's tiered bonus program. The annual base salary for the position is $165,000 to $195,000/yr., depending upon attorney experience, skills, and qualifications. Depending on billable hours, total compensation can range up to $207,000 for those at the lower end of the salary range to $245,000 at the higher end.

RESPONSIBILITIES

  • Manage and litigate complex trust, estate, and conservatorship disputes, including but not limited to (a) will and trust contests (e.g., undue influence, lack of capacity, fraud); (b) breach of fiduciary duty claims against trustees, executors, and conservators; (c) petitions for instructions and accountings; (d) spousal property petitions; (e) elder abuse actions (financial and physical); (f) conservatorship contested matters; (g) probate and trust administration disputes.
  • Conduct legal research and analysis, draft pleadings, motions, and briefs.
  • Handle all aspects of discovery, including propounding and responding to written discovery, and taking/defending depositions.
  • Prepare for and attend court hearings, mediations, arbitrations, and trials.
  • Communicate effectively with clients, opposing counsel, and court personnel.
  • Develop and implement effective case strategies.
  • Collaborate with partners and other attorneys on complex matters.
  • Mentor junior attorneys and support staff as needed.
  • Maintain accurate time records and ensure compliance with billing requirements.

QUALIFICATIONS:

  • Juris Doctor (J.D.) degree
  • Active membership in good standing with the California State Bar
  • Five or more (5+) years of demonstrable experience specializing in California Trust & Estates Litigation
  • Strong understanding of the California Probate Code, related statutes, and case law
  • Exceptional written and oral communication skills, with a proven ability to draft persuasive legal documents and advocate effectively in court
  • Excellent analytical, research, and problem-solving skills
  • Ability to manage multiple priorities, work independently, and meet deadlines in a fast-paced environment
  • Strong interpersonal skills and a client-focused approach
  • Experience with trial preparation and courtroom advocacy is highly preferred
  • A proven track record of successfully resolving complex litigation matters
  • Ability to work on a hybrid schedule requiring three (3) days in the office after ninety (90) days of employment

OTHER DETAILS

  • Salary of $165,000 - $195,000 (for minimum billables of 1610 hrs./yr.), depending upon attorney experience, skills, and qualifications.
  • Hybrid work schedule requiring three (3) days in office after ninety (90) days of employment
  • Comprehensive benefits package, including medical, dental, vision, and life insurance.
  • 401(k) plan
  • Generous paid time off and holidays.
  • Professionaldevelopment opportunities
  • A collegial and supportive work environment.
  • Opportunity for significant growth and advancement within the firm.

Candidates may apply for this position on LinkedIn, on the Hire Counsel website, or by direct e-mail to We at Hire Counsel cannot promise that a particular candidate will get the job or an interview, but we can promise that we will review all submitted resumes.

About Hire Counsel, a Purpose Legal Company

Hire Counsel, a Purpose Legal Company, is an agile legal talent agency. We build connections between legal professionals and our clients, some of the nation's largest law firms and legal departments (and some of the smallest). By connecting good lawyers with our clients, we help attorneys find a permanent home. We also provide individuals with the option to work on contract (temporary) assignments to aid their stability as they proceed with their job searches. Hire Counsel holds all resumes in the strictest confidence.

Not Specified
Customs Brokerage Manager
Salary not disclosed

Customs Manager

Location: South San Francisco, CA (Onsite)

Schedule: Monday–Friday, 8:00 AM – 5:00 PM

Employment Type: Full-Time, Exempt

Compensation Range: $82,500 – $128,000 annually


About the Organization

A global transport and logistics provider is seeking an experienced Customs Manager to oversee and manage local customs brokerage operations in South San Francisco. The organization operates in over 80 countries and delivers end-to-end supply chain solutions including transportation, freight forwarding, customs brokerage, and compliance services.


Position Summary

The Customs Manager is responsible for providing operational leadership and compliance oversight for local customs brokerage activities. This role ensures adherence to U.S. Customs and Border Protection (CBP) regulations, minimizes regulatory and financial risk, and supports efficient import/export processing.


This is a fully onsite leadership role requiring daily presence at the South San Francisco facility.


Responsibilities

• Supervise and manage local customs brokerage operations in alignment with CBP regulations and internal compliance standards

• Monitor transaction volume, reject rates, and entry accuracy

• Ensure timely filing of customs entries and payment of duties, taxes, and government obligations

• Conduct customs entry audits and compliance reviews

• Maintain documentation in accordance with 19 CFR 163

• Ensure responsiveness to CBP communications, notices, and directives

• Provide training and development to customs brokerage staff

• Optimize customs clearance processes to reduce delays and mitigate risk

• Manage relationships with customs authorities and clients

• Utilize ACE Secure Data Portal for compliance and reporting

• Ensure brokerage team has up-to-date access to CBP regulations and Harmonized Tariff Schedule


Required Qualifications

• Active U.S. Customs Broker License (Required)

• Minimum 5 years of experience in customs operations with management and compliance responsibilities

• In-depth understanding of U.S. Customs regulations, import requirements, and international trade practices

• Proficiency in customs valuation and classification methodologies

• Experience with customs automation systems and brokerage software

• Experience conducting audits and compliance assessments

• Strong leadership and team management skills

• Strong analytical and problem-solving abilities

• Excellent communication and interpersonal skills

• Fluent in English (oral and written)


Preferred Qualifications

• Bachelor’s degree in International Trade, Supply Chain Management, or related field

• Experience within global freight forwarding or logistics organizations

• Familiarity with Air & Sea freight forwarding brokerage environments


Compensation & Benefits

• Medical, dental, and vision insurance

• Prescription coverage

• Life insurance

• Short-term and long-term disability

• Health and flexible spending accounts

• 401(k) plan with company matching contributions (up to 5%)

• Paid time off, paid holidays, and floating holidays

• Wellness resources


Addison Group is an Equal Opportunity Employer. Addison Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws. Addison Group complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. Reasonable accommodation is available for qualified individuals with disabilities, upon request.

Not Specified
Senior Director Quality Assurance
Salary not disclosed
San Mateo, CA 3 days ago

*****EXCITING NEW OPPURTUNITY ******

Director/ Senior Director - Quality Assurance


We are partnered with a global biotech that is looking to expand their quality team by bringing in a director/senior director of quality assurance.


Their position focus will be supporting the development, coordination and implementation of global pharmacovigilance regulations related to quality assurance activities.


Key requirements-

  • 8-10 years of hands-on Global Pharmacovigilance experience within biotech/pharma environments
  • Proven track record supporting and leading FDA, EMA, and other global health authority inspections
  • Confident interacting directly with regulators and managing regulatory inquiries
  • Strong working knowledge of global GVP regulations and pharmaceutical quality standards
  • Experienced in conducting internal audits and maintaining an effective, inspection-ready QMS


Responsibilities-

  • Ensure global PV compliance (FDA, EMA, ICH)
  • Lead risk-based PV audits, CAPA management, and metric trending
  • Drive inspection readiness and serve as QA lead during health authority inspections
  • Oversee PV deviations and maintain effective quality systems documentation
  • Provide PV training, regulatory updates, and cross-functional compliance support
  • Support EU QPPV, reporting activities, and product complaint oversight
Not Specified
Manufacturing Technician
Salary not disclosed
San Mateo, CA 3 days ago

Manufacturing Technician - Machine Assembly & Test

Contract

Fremont, CA (Onsite)


This position pays around $28/hr - $32/hr on W2


Job Summary

The Manufacturing Technician will be responsible for the hands-on assembly, testing, and troubleshooting of their production systems. This role will involve working closely with engineers and other technicians to ensure the quality and performance of our machines. The ideal candidate possesses a strong mechanical aptitude, experience with assembly and testing processes, and a commitment to quality and safety.

Responsibilities

  • Assemble complex mechanical and electromechanical systems according to work instructions and engineering drawings.
  • Perform functional testing of assembled systems, including data collection and analysis.
  • Troubleshoot and diagnose mechanical and electrical issues.
  • Use hand tools, power tools, and precision measuring instruments to assemble and test equipment.
  • Read and interpret schematics, wiring diagrams, and assembly drawings.
  • Follow standard operating procedures (SOPs) and safety guidelines.
  • Maintain a clean and organized work area.
  • Collaborate with engineers and other technicians to improve assembly and test processes.
  • Document assembly and test results accurately.
  • Identify and report any quality issues or discrepancies.
  • Assist with the installation and commissioning of new equipment.
  • Contribute to a positive and collaborative team environment.


Qualifications

  • High school diploma or equivalent; technical certification or associate's degree in a related field is a plus.
  • 2+ years of relevant experience in manufacturing or a related field, preferably with experience in machine assembly and testing.
  • Strong mechanical aptitude and hands-on skills.
  • Experience with using hand tools, power tools, and precision measuring instruments (e.g., calipers, micrometers).
  • Ability to read and interpret schematics, wiring diagrams, and assembly drawings.
  • Familiarity with basic electrical and mechanical principles.
  • Excellent problem-solving and troubleshooting skills.
  • Ability to work independently and as part of a team.
  • Strong attention to detail and commitment to quality.
  • Good communication and interpersonal skills.
  • Experience with data collection and analysis is a plus.
Not Specified
Quality Assurance Program Manager
🏢 Barrington James
Salary not disclosed
San Mateo, CA 3 days ago

QA Program Manager – GCP / GLP / GVP



We are partnered with a well established Medical Device company looking to expand their Quality Assurance team.


They are seeking an experienced QA Program Manager, this individual will support the embedded Quality leadership across clinical, nonclinical, and pharmacovigilance programs from early through late-stage development.


Key Responsibilities

  • Lead and conduct GCP, GLP, and GVP audits
  • Provide hands-on QA support across study planning, execution, and close-out
  • Drive inspection readiness and support global regulatory inspections (FDA, EMA, ICH)
  • Lead deviation investigations, root cause analyses, and CAPA implementation
  • Oversee and qualify external vendors to ensure ongoing compliance


Profile

  • 7+ years’ QA experience in pharma, biotech, or medical device
  • Strong background supporting clinical, nonclinical, and PV activities
  • Proven audit leadership and regulatory inspection support
  • Experience in imaging agents, diagnostics, or combination products preferred
Not Specified
Commercial Lines Account Manager
Salary not disclosed
San Mateo, CA 3 days ago

Seeking a west coast P&C Account Executive for a national private equity-M&A practice for a top 5 broker in the world.


The primary role of the Account Executive is responsibility for placement and client management on an assigned book of business, as well as guiding the Service team.

The AE is responsible for a more complex book of business, based on industry specialty, account revenue size and/or coverage complexity, such as loss sensitive programs, large deductibles, captives or shared and layered programs.

Not Specified
Tech Trans Associate [Mid-level] @ Practice Leading Platform
Salary not disclosed
San Mateo, CA 3 days ago

Overview

Whistler Partners is partnering with a nationally recognized technology and life sciences law firm seeking a mid-level associate (3+ years) to join its world-class Technology Transactions practice.


This team handles complex, cutting-edge technology transactions for some of the most prominent technology, digital media, and consumer tech companies in the United States and internationally — from early-stage innovators to publicly traded market leaders.

The practice works closely with one of the top-ranked startup, IPO, and M&A corporate platforms in the country, offering associates meaningful exposure to the intellectual property and commercial aspects of transformative deals.


Why this role?

At the Center of Innovation

You’ll advise emerging and established technology companies on mission-critical commercial agreements, licensing arrangements, and strategic transactions involving high-value IP and data assets.


True Deal Adjacency

This practice works hand-in-hand with corporate teams on M&A, IPOs, and other major transactions. You’ll counsel on the intellectual property and commercial components of deals — not just standalone contracts.


Breadth Across Growth Stages

From startup technology companies to public enterprises, you’ll gain exposure across the full company lifecycle.


Platform Strength + Optionality

This is a nationally recognized tech transactions group within a broader firm known for its dominance in startup and life sciences work — a powerful foundation whether your long-term goal is partnership or in-house leadership.


Key Responsibilities

  • Draft and negotiate complex commercial and technology agreements
  • Advise on software licensing, IP commercialization, SaaS, data rights, and platform agreements
  • Support M&A and other corporate transactions on IP and commercial diligence and structuring
  • Counsel clients on contract and intellectual property strategy
  • Work closely with corporate teams advising startup, growth-stage, and public companies


Ideal Candidate Profile

  • 3+ years of substantial law firm experience in technology transactions
  • Strong grounding in intellectual property and contract law
  • Experience handling complex commercial agreements for technology companies
  • Exposure to IP and commercial aspects of M&A or other corporate transactions
  • Superior academic credentials
  • Excellent drafting, communication, and interpersonal skills
  • Barred in the jurisdiction of application or eligible to waive/sit for the next exam


Locations

Boston, New York, Silicon Valley, San Francisco, or Santa Monica.



About Whistler Partners

Matchmakers, Not Headhunters

Whistler Partners is a boutique matchmaking firm focused on counseling the best and the brightest attorneys over the course of their careers. We believe that the right move comes from working closely with talent to curate their long-term career paths. When it comes to career advice, what matters is not the size of the agency but the strength of your individual recruiter.


We readily admit that we are elite and only work with the best – after all, a little elitism is okay when it comes to your career. Employers love us because we are picky about whom we represent, and attorneys love us because we get them their dream jobs.

Not Specified
Quality Oversight Manager- Clinical Operations
Salary not disclosed
South San Francisco, CA 3 days ago
Quality Oversight Manager – Clinical Operations (Remote, Contract)

We are seeking an experienced Monitoring Quality Oversight Manager to support multiple oncology clinical trials for one of our growing biotech client. This role provides strategic and hands-on oversight of CRO monitoring activities to ensure data integrity, regulatory compliance, and high-quality trial execution. The position partners closely with Clinical Operations, CROs, and Quality teams to identify risks, implement best practices, and drive continuous improvement across studies.

Key Responsibilities

  • Perform monitoring quality oversight across multiple clinical studies

  • Develop and execute monitoring oversight plans and risk mitigation strategies

  • Review monitoring plans, reports, and trends; implement corrective actions as needed

  • Provide subject matter expertise to internal teams and external partners

  • Support SOP development, training initiatives, and inspection readiness

  • Present oversight findings and recommendations to leadership

  • Track monitoring metrics and follow up on CAPAs

Qualifications

  • Bachelor’s degree in life sciences or related field

  • 6+ years of biotech/pharma experience, including 3+ years in monitoring oversight

  • Oncology clinical trial experience required

  • Strong knowledge of GCP, ICH, and regulatory guidelines

  • Proven CRO oversight and stakeholder management experience

  • Excellent analytical, communication, and organizational skills

  • Ability to work independently in a fast-paced, remote environment

  • Willingness to travel up to 80%

Terms: This is a 12-month contractor position with an estimated pay range of $80-$100/hr DOE

Estimated Min Rate: $80.00
Estimated Max Rate: $100.00

What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

  • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
  • Health Savings Account (HSA) (for employees working 20+ hours per week)
  • Life & Disability Insurance (for employees working 20+ hours per week)
  • MetLife Voluntary Benefits
  • Employee Assistance Program (EAP)
  • 401K Retirement Savings Plan
  • Direct Deposit & weekly epayroll
  • Referral Bonus Programs
  • Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: 

Not Specified
Production Supervisor
Salary not disclosed
San Mateo, CA 3 days ago

Client: Medical Device


Details:

  • 6-Month contract with high potential of conversion
  • 40-Hours per week, on-site in SSF


Requirements:

  • 6+ years of experience in the medical device industry with at least 3 years of experience in a management, supervisory or lead role
  • Experience in building a production team and overseeing assembly team schedule
  • Hands-on experience with assembly, testing, or packaging of electromechanical or disposable medical devices
Not Specified
Senior Manufacturing Process Engineer
Salary not disclosed
San Mateo, CA 3 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
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