Top 110 Csv validation analyst Jobs

CSV Validation Analyst
Zifo —Emeryville, CA
- Full-time
- Hybrid work
- Computer Science
- 3 years
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Senior HEDIS Analyst/ Technical Lead - Denver Health Medical Plan (Must Live in Colorado. Weekly On-Site Requirement)
Denver Health —Denver, CO
- $91,000 - $141,000 a year
- Full-time
- Hybrid work
- Computer science
- Computer Science
- Pass drug screening
- Paid parental leave
- Paid holidays
Computer Systems Validation (CSV) Analyst
Brooksource —Concord, NC
- $70 - $90 an hour
- Full-time
- Background check
- In-person
- Senior level
- Health savings account
- Paid holidays
Quick Apply
3d
Principal Analyst, CGT Agentic Solutions
Vertex Pharmaceuticals —Boston, MA
- $142,800 - $214,200 a year
- Full-time
- Hybrid work
- Computer science
- Azure
- Computer Science
- Loan repayment program
- Dental insurance
Analyst - Computer Software Validation (Remote)
Veeva Systems —Remote
- $60,000 - $125,000 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
- Paid holidays
- Dental insurance
CSV Analyst
Katalyst Healthcares & Life Sciences —Dallas, TX
- Contract
- Hybrid work
- Computer Science
- 5 years
- Laboratory experience
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6d
Pricing Analyst - Contract
Designer Brands Inc. —Columbus, OH
- $20 - $25 an hour
- Contract
- Administrative experience
- Analysis skills
- Bachelor's degree
6d
CSV Analyst with Instrument integration & Validation expertise
Katalyst Healthcares & Life Sciences —Cincinnati, OH
- Contract
- Hybrid work
- Computer Science
- 5 years
- Laboratory experience
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Sr Computer Systems Validation Analyst
Novo Nordisk —Clayton, NC
- Customer service
- 5 years
- Writing skills
- Paid holidays
- Disability insurance
QMS & SAP Validation Analyst (Contract)
Kashiv BioSciences, LLC —Piscataway, NJ
- $65 - $75 an hour
- Extended hours
- Mid-level
- Master's degree
- Travel
Instrumentation Software Validation Analyst
Katalyst Healthcares & Life Sciences —Cincinnati, OH
- Contract
- Computer Science
- 5 years
- Laboratory experience
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6407 - Senior CSA Analyst – Plasma Systems & Site Enablement / Senior CSV Engineer
Verista, Inc. —King of Prussia, PA
- $70,491 - $118,060 a year
- Remote
- Computer Science
- Engineering
- Senior level
- Commuter assistance
- Paid parental leave
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Validation Test Analyst (CSV/CSA)
Cognizant —Chicago, IL
- $71,100 - $112,500 a year
- Full-time
- Remote
- Mid-level
- US work authorization
- Communication skills
- Paid parental leave
- Employee stock purchase plan
2d
Client Operations Analyst
BNY Mellon —Lake Mary, FL
- $28 - $35 an hour
- Contract
- Hybrid work
- Office
- Finance
- Bachelor's degree
- Health insurance
- Dental insurance
GMP Quality Control
MEDVACON Life Sciences —Lexington, MA
- Multiple hires
- Mid-level
- US work authorization
Quick Apply
Siemens Opcenter Validation Engineer
USDM Life Sciences —Los Angeles, CA
- $70 - $85 an hour
- Full-time
- Hybrid work
- 7 years
- Engineering
- Office
- Disability insurance
- Dental insurance
Quality Assurance Analyst
CSV-TAUREAN —San Antonio, TX
- PMP
- Mid-level
- 3 years
Global Quality System Developer and Validation Analyst (173581)
Colgate-Palmolive —Piscataway, NJ
- $86,000 - $121,000 a year
- Hybrid work
- Computer Science
- ERP systems
- 3 years
- Profit sharing
- Paid parental leave
Specialist IS Business Systems Analyst
Amgen —Holly Springs, NC
- $110,038.45 - $148,875.55 a year
- Doctoral degree
- Office
- Master's degree
- Disability insurance
- Health insurance
LIMS Analyst (LabVantage)
Zifo —Boston, MA
- Mid-level
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply

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CSV Validation Analyst

Zifo
Emeryville, CA

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Job Details

Full-time

Benefits

Health insurance
Dental insurance
Flexible spending account
Vision insurance
401(k) matching
Life insurance

Qualifications

Quality control corrective actions
Data integrity assurance
Instrumentation troubleshooting
Vendor selection
Laboratory equipment performance testing and validation
IT user and group management
Procedural guides
Operational management
Preventive action implementation
Laboratory instrument validation
Testing and evaluation
Equipment installation
Software implementation
Hardware maintenance
Configuration management
Equipment troubleshooting
Corrective and preventive actions (CAPA)
Operating system updates
FDA 21 CFR Part 11
GMP
Software installation
Enterprise software support
Data integrity and documentation
Laboratory equipment repair
Hardware support
Compliance documentation
Data access controls implementation
User acceptance testing
Vendor relationship management
Software documentation

Full Job Description

In this role, you will work both collaboratively within cross-functional teams — including colleagues, consultants, vendors, and MSPs — and independently to support day-to-day operations and project-based initiatives. The primary focus of the role is managing daily operational activities, including Tier 1 and Tier 2 IT Helpdesk support for end users and customers. Responsibilities include supporting lab equipment and applications (GMP and non-GMP), troubleshooting hardware and software issues, performing computer system validation activities (including change controls, validation execution, NCRs, AIRs, and CAPAs), maintaining data integrity and compliance, and administering system configuration, access management, security patching, and data backup processes. The ideal candidate is adaptable, service-oriented, and brings a broad technical skillset to effectively support evolving business needs. Hybrid schedule acceptable with a desire for 3-4 days onsite weekly.

Requirements

Execute & comply with SDLC, Change, Access, Inventory, & operational management procedures for business‑critical applications & platforms.
Support evaluation, pilot testing, selection, & ongoing management of IT vendors & partners aligned to business & compliance requirements.
Lead or support validation of computerized systems & laboratory instruments, including installation, configuration, troubleshooting, & documentation (SOPs, IQ/OQ/PQ).
Ensure ongoing data integrity, backup, & regulatory compliance for GMP laboratory & manufacturing systems.
Provide technical input & support for Investigations, Change Controls, CAPAs, decommissioning, & audit readiness activities.
Participate in or lead Periodic Reviews, User Access Reviews, & Audit Trail Reviews for GMP systems.
Execute & support UAT activities, collaborating with IT & business teams on issue resolution.
Deliver hands‑on operational support for QC & Manufacturing instrument systems, including break/fix support & reliability issues in validated & production environments.
Manage user account provisioning & deactivation in compliance with access control SOPs.

QUALIFICATIONS:

Education:

Bachelor’s degree in Information Technology, Computer Science, Life Sciences, or a related field with at least 5+ years of relevant experience in a laboratory environment or biotech/pharma setting; or

Experience:

Strong operational knowledge of laboratory IT environments, including instrument connectivity & client/server architectures.
Proficiency in Windows OS administration (registry, system files, security, local accounts & policies).
Working knowledge of network technologies (VLANs, firewalls, security protocols, instrument LANs).
Familiarity with virtualization platforms (e.g., VMware, Citrix VDI).
Experience supporting validated systems in a regulated GxP environment is required.
Knowledge of 21 CFR Part 11, Annex 11, data integrity, and CSV process

Benefits

CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 18 of the Top 20 Biopharma companies.

We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.

We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.

If you share these sentiments and are prepared for the atypical, then Zifo is your calling!

Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Quick Apply

Refine Your Search

csv validation analyst jobs

CSV Validation Analyst

Senior HEDIS Analyst/ Technical Lead - Denver Health Medical Plan (Must Live in Colorado. Weekly On-Site Requirement)

Computer Systems Validation (CSV) Analyst

Principal Analyst, CGT Agentic Solutions

Analyst - Computer Software Validation (Remote)

CSV Analyst

Pricing Analyst - Contract

CSV Analyst with Instrument integration & Validation expertise

Sr Computer Systems Validation Analyst

QMS & SAP Validation Analyst (Contract)

Instrumentation Software Validation Analyst

6407 - Senior CSA Analyst – Plasma Systems & Site Enablement / Senior CSV Engineer

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Client Operations Analyst

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Siemens Opcenter Validation Engineer

Quality Assurance Analyst

Global Quality System Developer and Validation Analyst (173581)

Specialist IS Business Systems Analyst

LIMS Analyst (LabVantage)

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