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Freelance Computer System Validation Csv Jobs in Rochester, NY

... Knowledge of computer applications and current software is desirable. • Knowledge of ... systems, and production equipment • Must be able to recognize situations where there is a ...

AI Engineer - Manufacturing Data

Rochester, NY · On-site

$113K - $135K/yr

Ensure all AI solutions are validated, documented, and auditable in a GxP/ISO environment ... Bachelor's degree in Engineering, Computer Science, Information Systems, Industrial Engineering, or ...

Box Truck Driver

Rochester, NY · On-site

$24 - $26/hr

... computer system. * Return all merchandise and completed forms to the designated check-in area. * Submit all paperwork to the Billing Department for verification and processing. Requirements: * Valid ...

... computer system. * Return all merchandise and completed forms to the designated check-in area. * Submit all paperwork to the Billing Department for verification and processing. Requirements * Valid ...

Knowledge of MS Word and comfortable with working with computer systems * Valid Driver's License * Early Childhood Experience * Great interpersonal and communication skills Job Type: Part-time, ...

Knowledge of MS Word and comfortable with working with computer systems * Valid Driver's License * Early Childhood Experience * Great interpersonal and communication skills Job Type: Part-time, ...

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Freelance Computer System Validation Csv information

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How much do freelance computer system validation csv jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for freelance computer system validation csv in Rochester, NY is $51.30, according to ZipRecruiter salary data. Most workers in this role earn between $38.89 and $62.36 per hour, depending on experience, location, and employer.

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.
What are the most commonly searched types of Computer System Validation Csv jobs in Rochester, NY? The most popular types of Computer System Validation Csv jobs in Rochester, NY are:
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What cities near Rochester, NY are hiring for Freelance Computer System Validation Csv jobs? Cities near Rochester, NY with the most Freelance Computer System Validation Csv job openings:
Infographic showing various Freelance Computer System Validation Csv job openings in Rochester, NY as of July 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% In-person job distribution, with an average salary of $106,711 per year, or $51.3 per hour.

Validation Technician

Unifin SAS

Rochester, NY • On-site

Full-time

Medical, Retirement

Re-posted 11 days ago


Job description

Validation Technician
Who we are?
We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients' lives to as many people as possible.
With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 employees.
Since 2013, our site Unither Manufacturing LLC. based in Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 300 employees.
Your role
Reporting to the Director of Quality,
JOB SUMMARY:
Assists validation efforts in many ways including the following: executes/supports equipment qualifications, cleaning validations and recertifications, chamber (i.e., freezers, refrigerators, incubators) recertifications, and process validations, takes and delivers samples, collects and compiles data for validation reports, assists in maintaining the Validation Document Library, maintains test equipment and department documentation.
ESSENTIAL FUNCTIONS / RESPONSIBILITIES:
• Assists in the execution of validation protocols ( qualification, process validations, and recertifications) for facilities, chambers, manufacturing equipment, manufacturing processes, cleaning, and critical utilities.
• Performs proper and timely post cleaning sampling from manufacturing equipment. Confirms there is an appropriate amount of required sampling materials and supplies available. Orders are to be placed as needed to ensure supplies are maintained. Responsible for organization of supplies and materials, FIFO is consistently followed..
• Maintains department documentation in an orderly library so that information can be provided to regulatory bodies in a timely manner. Participates in audits (i.e., customer and regulatory) and retrieves Validation documentation as requested.
• Ensures good documentation practices are followed during protocol executions, verifications, validation plans and summary reports generated during validation/ qualification activities are maintained according to procedure.
• Become proficient using temperature/humidity loggers along with the associated DT Pro software. Responsibilities will include, programing, reading, generating reports, as well as conducting routine maintenance per department procedure.
• Reviews documentation executed during validation activities and ensures completeness is performed contemporaneously. All applicable documentation is scanned and transferred to the activity's applicable project folder and all completed hardcopies are filed accurately within the site's documentation room.
• Ensures all department testing equipment is maintained in a current calibrated state. Communicates and works with outside vendors to schedule, ship, track, and receive testing equipment to be sent for calibration. Confirms a current calibration certificate is received with each piece of testing equipment. Inventory and calibration status is maintained within Blue Mountain Regulatory Asset Manager (BMRAM)..
Your profile
EDUCATION & EXPERIENCE:
• HS Diploma/GED with minimum 2 years of experience in a FDA regulated environment, GMP production setting preferred.
• AAS with 1 year experience in a FDA regulated environment, GMP production setting preferred.
• BS with 0 experience.
• Above average written communication skills & writing abilities.
• Basic mechanical knowledge and aptitude.
• Ability to learn the operation and function of multiple pieces of equipment.
• Use of basic hand tools such as wrenches, screwdrivers, measuring devices.
• Knowledge of computer applications and current software is desirable.
• Knowledge of manufacturing processes and demonstrated leadership capabilities are preferred.
• General understanding of material handling machinery is advantageous.
KNOWLEDGE SKILLS & ABILITIES:
• Demonstrated basic math skills in multiplication, division, percentage calculation, significant figures, conversion from metric to standard measures (or inverse), and weight to volume measures (or inverse). This would include basic algebra and geometry.
• Familiarity using MS Word and ExcelAn understanding of production activities and/or mechanical aptitude
• Knowledge of production equipment operations
• Knowledge of instrumentation, control systems, and production equipment
• Must be able to recognize situations where there is a potential impact on product quality, safety, identity and purity; seeking guidance where necessary to implement solutions to issues that are identified
• Ability and willingness to support transactional and administrative functions within the department.
• Requires good teamwork, excellent communication, interpersonal and organization skills.
SCOPE OF DECISION-MAKING: Decisions require some judgment and critical thinking ability. Perform repetitive or routine duties working from detailed instructions and under standard procedures. Requires making minor decisions.
Compensation range
20,19 - 25,00 USD
*The referenced compensation range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
A Smarter Total Compensation Package
At Unither, your base salary is just the beginning. Our Total Rewards include:
  • 100% employer-paid medical premiums (a $2,000-$6,000+ annual value)
  • 401(k) contributions: 6% match plus an additional 4% company-funded contribution
  • HSA contributions with wellness incentives
  • Annual performance bonuses and merit increase eligibility
  • And more-because we invest in your health, your future, and your peace of mind.

It's a package designed to reward impact-not just hours worked.
More Than Just a PaycheckAt Unither, we don't just offer competitive hourly wages-we also pay 100% of your medical premiums. That means no paycheck deductions for your healthcare, which can be worth an extra $1 to $3.50 an hour in your pocket compared to jobs where you pay part of the premium.
Learn more about us:
We are a dynamic company driven by a spirit of victory and are therefore pursuing strong growth while maintaining a close relationship with our customers and employees.
Our culture is based on 5 values: Respect, Responsibility, Trust, Courage and Innovation. We are committed to bringing these values to life with our employees by granting them a high degree of autonomy in the exercise of their profession and by encouraging their initiatives.
We are committed to providing them with working conditions and atmosphere that is conducive to their development and the expression of their potential.
We propose you to integrate a site that values the meaning of work and that entrusts our employees with a high level of responsibility.
Join us and make a difference!
Unither is an Equal Opportunity Employer. We are committed to providing reasonable accommodations for qualified individuals with disabilities and to ensuring equal employment opportunity for all applicants.