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Usps Jobs in San Ramon, CA (NOW HIRING)

Cushman & Wakefield

Receptionist

San Francisco, CA · On-site

$26.56 - $31.25/hr

Delivery and pick up USPS and accountable mail (Fed Ex, UPS, DHL, messenger, and other incoming packages throughout floors to and from mailroom-Deliver print work as needed * Process all outgoing ...

Stable

Product Operations

San Francisco, CA · On-site

$130K - $200K/yr

Manage regulators + vendor: work with Product, Address Network, and Mail Operations to maintain USPS compliance, own product-facing relationships with financial institutions, interface with product ...

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Usps information

What is a USPS job?

A USPS job refers to a position with the United States Postal Service, which is responsible for mail delivery and related services in the U.S. USPS offers a variety of roles, including mail carriers, clerks, and mail processors. These jobs typically provide competitive pay, benefits, and job stability. Employees may work in post offices, mail sorting facilities, or deliver mail on designated routes.

What are the key skills and qualifications needed to thrive in the Usps position, and why are they important?

To thrive at USPS (United States Postal Service), you need strong organizational abilities, attention to detail, physical stamina, and a valid driver’s license for most delivery positions. Familiarity with mail sorting equipment, handheld scanners, and basic computer systems is often necessary. Excellent customer service, time management, and the ability to work independently are standout soft skills for this role. These competencies ensure accurate, timely mail delivery and a positive experience for customers in a fast-paced environment.

What does a typical workday look like for a USPS employee?

A typical workday for a USPS employee often starts with sorting mail and parcels, organizing delivery routes, and loading vehicles with outgoing mail. Throughout the day, you may deliver mail to homes and businesses, interact with customers, handle packages of various sizes, and ensure accurate, on-time delivery. The work can involve being outdoors in different weather conditions and adhering to established schedules and safety guidelines. Teamwork and open communication with supervisors and coworkers are also an important part of the job, especially when coordinating large volumes of mail or adjusting to route changes. Overall, the role offers variety and the chance to serve your local community every day.

What are popular job titles related to Usps jobs in San Ramon, CA? For Usps jobs in San Ramon, CA, the most frequently searched job titles are:
What cities near San Ramon, CA are hiring for Usps jobs? Cities near San Ramon, CA with the most Usps job openings:
Usps jobs near you
Infographic showing various Usps job openings in San Ramon, CA as of July 2026, with employment types broken down into 70% Full Time, 20% Part Time, and 10% Contract. Highlights an 100% In-person job distribution.
Sr. Pharmacovigilance (PV) Clinical Scientist

Sr. Pharmacovigilance (PV) Clinical Scientist

Software Guidance & Assistance

South San Francisco, CA • On-site

Other

Posted 5 days ago

Job description

Software Guidance & Assistance, Inc., (SGA), is searching for a Sr. Pharmacovigilance (PV) Clinical Scientist for a CONTRACT assignment with one of our premier Pharmaceutical clients in South San Francisco, CA .
The US Patient Safety Sr. PV Clinical Scientist - Pharmacovigilance (PV) Compliance Team performs the tactical and operational job responsibilities, including but not limited to the collection, clinical review, evaluation, and processing of adverse event (AE) information received by US Patient Safety. The Sr. PV Clinical Scientist leads clinical review of USPS cases (processed in-house or externally by the vendor) and supports the US Patient Safety PV Clinical Associate Group Director and PV Clinical Group Director-PV Compliance Team in all activities. All responsibilities are performed under the direction of the US Patient Safety PV Clinical Management. Contributes in depth knowledge of Individual Case Safety Reports (ICSRs) case processing. Has developed a variety of skills typically gained through years of professional experience. Works autonomously with minimal supervision. May lead or contribute with skills to projects. May act as coach for colleagues with less experience and provide guidance.
Responsibilities :
  • Completes drug safety monitoring and tracking in a timely, thorough and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations and Genentech/Roche Standard Operating Procedures (SOPs)
  • Reviews, evaluates, and verifies potential AE information during triage to determine required action per internal policies and procedures and perform data entry of adverse events by timely completion of the case via Roche global safety database. Performs seriousness / validity/causality and conducts quality review of all cases (as applicable) based on their medical assessment
  • Performs labeling assessment for AE(s) received using clinical knowledge and conducted follow up for all reported cases (as applicable)
  • Responsible for leading efforts to ensure quality of Individual Case Safety Reports (ICSRs) is at par with company standards
  • Responsible for maintaining thorough knowledge of ICSR requirements for assigned Therapeutic Areas (TA)
  • Performs trend analysis of vendor case processing issues for assigned TA and escalates to vendor, TA Leads and USPS management as applicable
  • Update and create SOPs; lead process improvement initiatives
  • Responsible for developing executive summary on the quality trends observed on a quarterly basis
  • Ensures quality of Health Authority (HA) submissions is at par with local regulations
  • Responsible for Clinical Review of cases processed in-house and by vendors
  • Understands case processing data to evaluate error rates and potential compliance impact
  • Responsible for training internal USPS and/or vendors staff or team and ensure PV compliance
  • Collaborate with departments and partners on drug safety data exchange
  • Responsible for ensuring appropriate data correction in the safety database for identified issues or errors
  • Responsible for maintaining follow-up templates, ensuring successful transmission of all follow-up attempts performed by PV Compliance Team Scientist /Vendor staff via the correspondence module
  • Accountable for training internal and external staff members on using correspondence module ? Performs reconciliation of outgoing communications
  • Maintains robust knowledge of Technical Product Complaints (TPC) & Medical Product Complaint (MPC) for all company products including combination products
    • Responsible for ensuring all product complaints are reported to the appropriate stakeholders within defined timelines
  • Ensures appropriate due diligence to obtain missing and/or additional information for Adverse Events (AEs) is performed in accordance with company SOPs / local and global regulations
    • Escalates any issues pertaining to follow up activities and provide strategic resolution to USPS management
  • Assists USPS management in maintaining oversight for GVP vendors
    • Identifies the risks and gaps pertaining to case processing for GVP Vendors
    • Continuously monitors feedback to inform quality improvements and updates
  • Responsible for performing impact assessment for any new / updated company SOPs or Health Authority requirements pertaining to ICSR processing and implements any process changes required based on the identified impact
  • Responsible for identifying and developing training documents (i.e., SOPs) for the targeted audience (as needed)
  • Assists in AE reconciliation activities and/or Case Transmission Verification (CTV) (as applicable)
  • Acts as single point of contact with key stakeholders for safety-related activities, identifies potential business gaps, and assists in the development and implementation of process solutions, and leads projects as assigned and under the direction of the US Patient Safety PV Clinical management
  • Responsible for the preparation and development of Patient Safety presentations and participates in the education offer internal /external stakeholders/vendors as applicable
  • Acts as Subject Matter Expert (SME) for safety-related activities within Global Safety Database per Genentech/Roche SOPs
  • Provide support during audits and inspections
  • Collaborates with other patient safety teams as needed

Required Skills :
  • Demonstrates capability to comprehend medical information
  • Demonstrates ownership, initiative and accountability
  • Sound decision-making abilities as demonstrated by systematic gathering of information, appropriately assessing the complexity of issues, and prioritization of tasks in a timely manner within the scope of responsibility
  • Demonstrates strong, dynamic leadership skills
  • Works well independent or within teams and is effective in collaborating with others internally and externally Ability to exercise independent judgment and discretion in matters of significance
  • Ability to work on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.
  • Communication and presentation skills; highly effective at summarizing and presenting key considerations and decision-points
  • Ability to flex and thrive in an agile and fast-changing environment
  • Strong attention-to-detail
  • Strong attention-to-detail in establishing priorities and meeting deadlines
  • Strong project management skills
  • Ability to travel domestically and internationally as per business needs
  • Health Care Professional degree (e.g., RN/BSN/MSN, NP, RPh/B Pharm/Pharm D, or MD)
  • Minimum 5 - 7 years of experience in a biopharma company with Pharmacovigilance responsibilities (Preferred); OR equivalent clinical experience with thorough understanding of FDA safety regulations, ICH guidelines, and other applicable regulatory guidance documents, global PV regulatory environment, EMA regulations
  • Writing experience; science/medical writing
  • Computer proficiency and Data entry experience
  • Project Management

SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work. Please find us at .
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
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