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Freelance Computer System Validation Csv Jobs in Puerto Rico

JC Automation Corp

PR · On-site

$18/hr

Engineering Project Support: Assist in the management and execution of assigned engineering projects, including automation implementations and computer system validation (CSV) activities, under the ...

JC Automation Corp

PR · On-site

$18/hr

Engineering Project Support: Assist in the management and execution of assigned engineering projects, including automation implementations and computer system validation (CSV) activities, under the ...

Mirus Consulting Group

Project Manager

Manati, PR

The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States.

FITS LLC

Sr. Manufacturing Engineer- 149

Juncos, PR · On-site

$88K - $121K/yr

Performing and applying knowledge of Computer System Validation (CSV) * Executing documentation changes The Personality Part: * Our Next Piece is someone who treats everyone they meet like family ...

PACIV

Automation Engineer

San Juan, PR · On-site

Experience with computer systems validation (CSV) in regulated/GMP environments. Desired Soft Skills: * Strong problem-solving, communication, leadership, and teamwork skills. * Ability to manage ...

JC Automation Corp

PR · On-site

$25 - $35/hr

Exposure to Computer System Validation (CSV) activities and documentation. * Familiarity with OSI PI historian or equivalent data contextualization platforms. * Prior experience in a pharmaceutical ...

PACIV

Senior Automation Technician

San Juan, PR · On-site

$102K - $133K/yr

Bachelor's degree in Engineering (Electrical, Computer, Mechanical) or equivalent experience ... Experience supporting automation system validation (CSV) and documentation tools such as Kneat.

Validation & Engineering Group, Inc

PR

$57K - $58K/yr

Associate CSV - Periodic Review Scientist Position Summary The Associate CSV Periodic Review ... computer systems to ensure compliance with regulatory requirements and maintenance of the validated ...

FITS LLC

Sr. Quality Specialist/Engineer

Juncos, PR · On-site

$86K - $117K/yr

Execute and support Computer Systems Validation (CSV) activities. * Ensure compliance with quality systems, procedures, and applicable regulations. * Collaborate with cross-functional teams to ...

Validation & Engineering Group, Inc

PR

$59K - $60K/yr

Associate CSV - Periodic Review Scientist Position Summary The Associate CSV Periodic Review ... computer systems to ensure compliance with regulatory requirements and maintenance of the validated ...

Mirus Consulting Group

Sr. Engineer

Juncos, PR · On-site

$101K - $139K/yr

The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States.

Mirus Consulting Group

Sr. Engineer

Juncos, PR

$101K - $139K/yr

The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States.

JC Automation Corp

PR · On-site

$80K - $105K/yr

MES software migration and Computer System Validation (CSV) lifecycle * cGMP, 21 CFR Part 11, and Data Integrity compliance for electronic systems * C&Q RFP development and vendor management * Change ...

JC Automation Corp

PR · On-site

$18 - $25/hr

Knowledge of Computer System Validation (CSV) requirements and documentation. * Prior experience with system administration tasks for GxP computerized systems. * Familiarity with CMMS tools for ...

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Freelance Computer System Validation Csv information

What is a Freelance Computer System Validation (CSV) specialist?

A Freelance Computer System Validation (CSV) specialist is an independent professional who ensures that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, comply with industry standards and regulatory requirements. CSV specialists test and document that software and hardware systems function as intended, are reliable, and meet compliance guidelines like FDA 21 CFR Part 11 or EU Annex 11. As freelancers, they work on a contract basis, often supporting multiple clients, and may help design validation strategies, conduct risk assessments, and prepare necessary documentation for audits and inspections.

What are the key skills and qualifications needed to thrive as a Freelance Computer System Validation (CSV) specialist, and why are they important?

To thrive as a Freelance Computer System Validation (CSV) specialist, you need expertise in regulatory compliance (such as FDA 21 CFR Part 11), validation protocols, and risk-based validation methodologies, often supported by a degree in life sciences, engineering, or IT. Familiarity with industry-standard validation tools, software testing platforms, and knowledge of GxP systems as well as certifications like PMP or GAMP are commonly required. Strong project management, analytical thinking, and effective communication skills set top performers apart in client-facing freelance environments. These competencies are crucial for ensuring validated systems meet strict regulatory requirements while efficiently managing projects and client expectations.

What are some common challenges faced by freelance Computer System Validation (CSV) specialists, and how can they effectively overcome them?

Freelance CSV specialists often encounter challenges such as adapting to diverse client systems, staying updated with evolving regulatory requirements, and managing multiple projects simultaneously. To overcome these, it's important to maintain strong communication with client teams, invest in ongoing professional development, and utilize project management tools to keep workflows organized. Additionally, building a network with other CSV professionals can provide valuable support and industry insights.
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Freelance Computer System Validation Csv jobs near you

Dynamic Program - Automation & PLC Training

JC Automation Corp

PR • On-site

$18/hr

Full-time

Posted yesterday

Job description

About Company:

JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.

ABOUT THE ROLE

Dynamic is JCA's multi-week professional development program designed to provide comprehensive, hands-on training to the next generation of Automation and PLC professionals. Built specifically for recent graduates, this program bridges the gap between academic knowledge and real-world industry application — combining an intensive 3-week training bootcamp with 1.5 years of project-based work experience across diverse client locations.

Participants will work alongside experienced engineers and automation specialists, gaining direct exposure to live projects in regulated pharmaceutical and industrial environments. With a strong emphasis on PLC programming, FDA compliance, GMP principles, and safety protocols, Dynamic equips emerging professionals with the technical foundation and professional confidence to build a meaningful career in industrial automation.

This is a full-time position. No prior work experience is required — Dynamic is designed precisely for those ready to launch their careers with purpose.

RESPONSIBILITIES

  • Intensive Training Participation: Complete an intensive 3-week training program covering critical topics in PLC systems, automation fundamentals, regulatory compliance, GMP principles, and safety protocols in industrial environments.
  • Project-Based Field Work: Collaborate with experienced engineers and automation specialists on real projects across multiple client locations, gaining direct hands-on experience in automation and computerized system environments.
  • Regulatory Compliance: Ensure adherence to FDA regulations, applicable safety standards, and industry compliance requirements throughout all assigned project activities.
  • Engineering Project Support: Assist in the management and execution of assigned engineering projects, including automation implementations and computer system validation (CSV) activities, under the guidance of senior team members.
  • Multi-Site Adaptability: Demonstrate flexibility and professionalism by working across diverse project sites and adapting to varying client environments, schedules, and technical requirements throughout the 1.5-year program commitment.

WHAT YOU'LL GAIN

  • Hands-on experience with real automation and PLC projects from day one.
  • Direct mentorship and guidance from experienced engineers and industry specialists.
  • Exposure to FDA-regulated pharmaceutical and industrial manufacturing environments.
  • Development of a strong technical foundation in PLC programming, GMP, safety, and compliance.
  • Professional growth support — including career orientation, goal-setting, and advancement guidance throughout the program.
  • A clear pathway toward a full-time professional role in industrial automation upon program completion.

REQUIREMENTS & QUALIFICATIONS

Required

  • Associate's degree in Science, Instrumentation, Control Systems, Electronics, or a related technical discipline.
  • No prior work experience required — this program is designed specifically for recent graduates.
  • Strong problem-solving skills and a genuine eagerness to learn in a technical environment.
  • Excellent communication and teamwork skills.
  • Flexibility and willingness to relocate and work across multiple project sites during the 1.5-year program commitment.
  • Bilingual in English and Spanish (oral and written).

Preferred

  • Basic familiarity with PLC concepts, ladder logic, or control systems through coursework or academic projects.
  • Exposure to industrial automation, instrumentation, or process control in an academic or lab setting.
  • Knowledge of GMP principles or regulatory frameworks through coursework.

SKILLS

Technical Skills

  • PLC systems — foundational programming and troubleshooting (developed through program)
  • Automation and control system fundamentals
  • FDA regulations and compliance requirements — awareness level
  • Good Manufacturing Practices (GMP) — principles and application
  • Safety protocols and best practices in industrial automation environments
  • Computer System Validation (CSV) — introductory support level
  • Microsoft Office Suite — Word, Excel, PowerPoint, Outlook

Soft Skills

  • Eager to learn and grow in a technically demanding, fast-paced environment
  • Strong critical thinking and analytical problem-solving approach
  • Collaborative team player who communicates clearly and professionally
  • Adaptable and open to working across different sites, teams, and project types
  • Reliable, accountable, and committed to the full program duration
  • Self-motivated with a proactive attitude toward professional development