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

MEDVACON

Medical Affairs Manager [515]

Foster City, CA · Hybrid

Company Description MEDVACON Life Sciences works with many leading pharmaceutical companies to hire contractors for projects & assignments in cGMP Quality, Compliance, Validation and CSV work. We're ...

7N USA, Inc.

IT Business Analyst

South San Francisco, CA · On-site

Demonstrate knowledge of current GxP requirements and documentation standards, with the ability to write Computer System Validation (CSV) documents and test protocols. -Requirements Management: Track ...

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All JobsCsv Validation JobsCsv Validation Jobs in San Ramon, CA

Csv Validation information

See San Ramon, CA salary details

$25

$58

$87

How much do csv validation jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for csv 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 key skills and qualifications needed to thrive in the csv validation position, and why are they important?

To excel in CSV Validation, a strong background in life sciences, engineering, or a related technical discipline is essential, along with knowledge of computer system validation regulations and best practices. Familiarity with FDA 21 CFR Part 11, GAMP guidelines, and validation software tools is highly valued, and certifications such as PMP or CISA can be beneficial. Attention to detail, analytical thinking, and effective communication skills help professionals manage documentation and collaborate with cross-functional teams. These abilities ensure that systems in regulated environments are compliant, reliable, and meet industry standards for quality and data integrity.

What are the typical daily responsibilities of a csv validation professional?

CSV (Computer System Validation) Validation professionals are responsible for planning, executing, and documenting validation activities for computerized systems used in regulated industries like pharmaceuticals and biotechnology. Their daily tasks include reviewing system requirements, developing validation protocols, conducting risk assessments, performing validation testing, and documenting results in accordance with regulatory standards. They regularly collaborate with IT, quality assurance, and business stakeholders to ensure systems are compliant and audit-ready. Staying organized and detail-oriented is crucial, as each step must be carefully documented and verified for compliance. This role is dynamic and requires balancing technical tasks with frequent cross-functional communication.

What is a csv validation?

A CSV Validation job involves verifying the accuracy, consistency, and integrity of data within CSV files. This role ensures that the data conforms to predefined formats, standards, and business rules. It often includes checking for missing values, incorrect data types, and formatting errors to prevent issues in data processing. Professionals in this role may use scripts, validation tools, or manual reviews to ensure data quality and compliance.

What are popular job titles related to Csv Validation jobs in San Ramon, CA? For Csv Validation jobs in San Ramon, CA, the most frequently searched job titles are:
What job categories do people searching Csv Validation jobs in San Ramon, CA look for? The top searched job categories for Csv Validation jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Csv Validation jobs? Cities near San Ramon, CA with the most Csv Validation job openings:
Csv Validation jobs near you
Infographic showing various Csv Validation job openings in San Ramon, CA as of August 2026, with employment types broken down into 89% Full Time, 3% Part Time, and 8% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $120,862 per year, or $58.1 per hour.

Medical Affairs Manager [515]

MEDVACON

Foster City, CA • Hybrid

Contractor

Re-posted 22 days ago

Job description

Company Description

MEDVACON Life Sciences works with many leading pharmaceutical companies to hire contractors for projects & assignments in cGMP Quality, Compliance, Validation and CSV work.

We're supporting our client in Foster City CA to hire contractors for several roles.  This is an outstanding opp to work with colleagues across different therapy areas and functional teams (Clinical Operations, Business Conduct, etc)

Job Description
  • Provide guidance and oversight related to health authority (FDA, EMA, MHRA, etc.) regulations that impact the Medical Affairs organization.
  •  May assist in development or review of Medical Affairs SOPs and other procedural documents.
  • Participates in developing and presenting training using standard modules and training on compliance related topics.
  • Participates in the periodic assessment and review of Medical Affairs GxP role-based training plans to suggest improvements to existing curriculums.
  • Assists in audit readiness for regulatory agency inspections
  • Supports Medical Affairs with internal or external routine audit activities and document reviews.
  • Ability to work hybrid if local to the site only - NO Full remote 
     
Qualifications

Exp in a pharma Medial Affairs lead role.

Ability to work W2 only
$45 ph
Excellent written/oral communication skills.

Solid organizational & planning skills.

Excellent problem-solving skills

Additional Information

Please attach a WORD resume to your submission

All of your information will be kept confidential according to EEO guidelines.

ON-SITE only on W2

This is a contract role and does not offer benfits

40-hour week


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