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Contract Validation Jobs in San Ramon, CA (NOW HIRING)

Fladger Associates

Validation Engineer

Fremont, CA · On-site

Fremont, CA Contract Duration: 3-24 months Rate: Negotiable Responsibilities: * Excellent employment opportunity for a Validation Engineer in the Fremont, CA area. * Manage and participate actively ...

MasTec Inc

Contract Specialist

Dublin, CA · On-site

$45 - $55/hr

Responsible for invoice validation and related communications with both vendors and internal customers associated with Construction Services activities. * Regular use of Salesforce / Conga contract ...

Intren West

Contract Specialist

Dublin, CA · On-site +1

$45 - $55/hr

Responsible for invoice validation and related communications with both vendors and internal customers associated with Construction Services activities. * Regular use of Salesforce / Conga contract ...

MasTec Inc

Contract Specialist

Dublin, CA · Hybrid

$45 - $55/hr

Responsible for invoice validation and related communications with both vendors and internal customers associated with Construction Services activities. * Regular use of Salesforce / Conga contract ...

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All JobsContract Validation JobsContract Validation Jobs in San Ramon, CA

Contract Validation information

See San Ramon, CA salary details

$25

$58

$87

How much do contract validation jobs pay per hour?

As of Jun 28, 2026, the average hourly pay for contract validation in San Ramon, CA is $58.11, according to ZipRecruiter salary data. Most workers in this role earn between $44.04 and $70.67 per hour, depending on experience, location, and employer.

What are the main challenges faced in a Contract Validation role, and how can I prepare for them?

One of the main challenges in a Contract Validation role is ensuring that all contract terms comply with legal, regulatory, and company requirements, which often involves scrutinizing complex and lengthy documents under tight deadlines. You'll also need to coordinate with multiple departments—such as legal, finance, and procurement—to clarify contract language and resolve discrepancies. To prepare, develop strong attention to detail, effective communication skills, and a solid understanding of relevant laws and industry standards. Familiarity with contract management software can also give you an edge in streamlining validation processes.

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

To thrive in Contract Validation, you need a strong understanding of legal terminology, contract law, and document analysis, often supported by a degree in law, business, or a related field. Familiarity with contract management software, document tracking systems, and compliance tools is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying discrepancies and collaborating with stakeholders. These skills ensure contracts are accurate, compliant, and enforceable, reducing legal risks and supporting organizational goals.

What is contract validation?

Contract validation is the process of ensuring that a contract is legally binding, accurate, and aligns with all relevant laws and organizational requirements. This involves reviewing the contract’s terms and conditions, verifying the parties involved, and checking for any errors or ambiguities. Contract validation helps prevent legal disputes and ensures all parties agree to clear, enforceable terms before signing. It is a crucial step in risk management for businesses and organizations.
What are the most commonly searched types of Validation jobs in San Ramon, CA? The most popular types of Validation jobs in San Ramon, CA are:
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What job categories do people searching Contract Validation jobs in San Ramon, CA look for? The top searched job categories for Contract Validation jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Contract Validation jobs? Cities near San Ramon, CA with the most Contract Validation job openings:
Contract Validation jobs near you
Infographic showing various Contract Validation job openings in San Ramon, CA as of June 2026, with employment types broken down into 64% Full Time, and 36% Contract. Highlights an 84% In-person, 2% Hybrid, and 14% Remote job distribution, with an average salary of $120,862 per year, or $58.1 per hour.
Senior Validation Engineer

Senior Validation Engineer

AstraZeneca

Redwood City, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 73 rated pharmaceutical

Job description

Role is heavily focused to support the key site digital/software/automation transformation and related validation activities. The first two years will focus on validation of digital tools (MES systems, software, etc) and may require continued administrative support of this system.
Responsible to perform adequate and comprehensive qualification and validation of equipment, processes, products, and facilities at the Redwood City site to support the site goals and targets.
Responsible for assuring the design, installation, implementation, data integrity and validation of computer systems meet all applicable industry standards and regulatory requirements to support the site goals and targets.
System or business owner and oversee the system from implementation ensuring proper documentation at every phase.
Key Accountabilities:
  • Work effectively with others from diverse backgrounds and demonstrate capability to adapt to new, different, or changing requirements. Display strong moral principles and work ethics while demonstrating initiative. Maintain a professional presence and display responsible behaviors
  • Support implementation of the Site Digital Technology Strategy and roadmap: architect key strategic digital transformation initiatives aligned to business priorities and value targets.
  • Knowledge and experience developing and leading CSV and Life-cycle management activities to support GxP conforming systems, facilities, manufacturing and laboratory systems
  • Evaluate equipment and processes to identify critical parameters based upon potential impact on product quality attributes
  • Prepare qualification, requalification, and process validation protocols, analyzes applicable data, and prepares final reports in compliance with relevant regulations, industry practices, and AZ policies and procedures
  • Perform and document field verification of equipment, instruments, and facilities as required by approved protocols
  • Assess accuracy of P&ID, Electrical drawing to support validation and change control
  • May provide supervision and training for less experienced or entry-level validation personnel, including review and enhancement of draft protocols, oversight of data collection, review/approval of raw data and assembled qualification packages
  • Provide supervision and training for contract validation personnel, including review and enhancement of draft protocols, oversight of data collection, review/approval of raw data and assembled qualification packages
  • Perform risk assessment on proposed changes, document change control deliverables with respect to validation requirements
  • Complete, review, and/or approve risk assessments for instruments, equipment, processes, and products.
  • Analyze data and information to determine whether processes, equipment, and products are within an appropriate state of control during qualification and validation as well as in assessing the need for requalification / revalidation on a periodic basis
  • Prepare and/or evaluate change controls to ensure that equipment, products, processes, and facilities remain in qualified, validated state, including definition of appropriate requirements in change control documents, completion of identified action, and preparation of applicable reports and data packages
  • Identify and investigate unusual or unexpected events, data, or sources of variation during the development and performance of qualifications/validations; assess and document the impact upon qualification or validation as applicable, and recommend appropriate corrective/preventive actions
  • Coordinate assigned qualification projects as needed with other departments as needed
  • Ensure that work is performed in accordance with applicable regulations, industry guidelines and practices, approved procedures and cGMP
  • Other responsibilities as assigned by department management

Essential Requirements:
  • Entry-level Master's/ PhD degree in engineering, science, technology, or related field (OR) Bachelor's degree with 3+ years of relevant experience.
  • At least 3 years' experience in independent development, writing and performance qualifications / validation
  • Experience in and knowledge of qualification of control systems and computer system validation
  • Proven capability to assess processes, equipment and products for sources of variation
  • Ability to analyse data and reach appropriate solutions
  • Ability to perform and appropriately document deviations and investigations
  • Must have excellent analytical skills and attention to detail. Work requires a high degree of accuracy in complex documentation; Able to work cooperatively and provide direction, as appropriate, to other members of the Validation Team, Engineering, Quality, and Manufacturing in the design and performance of qualification and validations.
  • Must have the ability to learn technical subject matter quickly and integrate knowledge into previously known information
  • Must effectively evaluation information collected from various sources and determine impact upon controlled state of processes, equipment, facilities, and products
  • Must be goal oriented and quickly adaptable to new situation
  • Excellent technical writing and verbal communication skills.
  • Must be goal oriented and quickly adaptable to new situation
  • Excellent technical writing and verbal communication skills
  • Experience with Process Engineering or setting up new equipment- (URS, PID, DQ, IQ, OQ, PQ)
  • Experience working with digital tools and applications related to reporting, documentation, and analysis.

Preferred Qualifications:
  • Ability to read P&IDs and electrical drawings
  • Working knowledge of FDA guidance on Process Validation and Computer System validation
  • Experience with various programming to support digital/software validation

Knowledge of hardware and/or software integration
The annual base pay (or hourly rate of compensation) for this position ranges from $ 101,643.20 - $152,464.80. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
23-Jun-2026
Closing Date
09-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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