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Computer System Validation Manager Jobs in Miami, FL

Aequor Inc

Validation Engineer

Davie, FL · On-site

Validation Engineer 1 Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to ...

St. Thomas University

System Analyst

Miami Gardens, FL · On-site

Perform systems management and integration functions, improve existing computer systems, and review computer system capabilities, workflow, and schedule limitations. Analyze or recommend commercially ...

St. Thomas University

System Analyst

Opa Locka, FL

Perform systems management and integration functions, improve existing computer systems, and review computer system capabilities, workflow, and schedule limitations. Analyze or recommend commercially ...

VIVEX BIOLOGICS INC

Validation Engineer II

Miami, FL · On-site

This includes leading and/or supporting validation of processes, equipment, and computer systems ... Communicate to management of performance against project plan. * Perform data and technical ...

EōS Fitness

Fitness Manager

Kendall, FL · On-site

$60K/yr

Must have valid PT certification. * Previous sales experience required. * Ability to work in a gym ... Ability to access and operate the Company computer system including preparing documents, entering ...

Steve Madden

Store Assistant Manager

Miami, FL · On-site

$15.75 - $21.25/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

Steve Madden

Store Assistant Manager

Aventura, FL

$15.75 - $21.25/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

Steve Madden

Store Assistant Manager

Aventura, FL · On-site

$15.75 - $21.25/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

Steve Madden

Store Assistant Manager

Pembroke Pines, FL · On-site

$15 - $20.25/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

Steve Madden

Store Assistant Manager

Miami, FL · On-site

$15.75 - $21.25/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

Dolce Vita

Store Assistant Manager

Aventura, FL · On-site

$15.75 - $21.25/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

Steve Madden

Store Assistant Manager

Miami, FL · On-site

$15.75 - $21.25/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

Steve Madden

Store Assistant Manager

Sunrise, FL · On-site

$15.50 - $20.75/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

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Computer System Validation Manager information

See Miami, FL salary details

$45.4K

$100.8K

$153.5K

How much do computer system validation manager jobs pay per year?

As of Jun 4, 2026, the average yearly pay for computer system validation manager in Miami, FL is $100,824.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,300.00 and $126,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Computer System Validation Manager, and why are they important?

To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.

What are some common challenges a Computer System Validation Manager faces during system implementation projects?

A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.

What does a Computer System Validation Manager do?

A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.

What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?

AspectComputer System Validation ManagerComputer System Validation Specialist
CertificationsGAMP, CQE, CSQEGAMP, CQE, CSQE
Work EnvironmentManagement, oversight, strategic planningExecution, testing, documentation
Industry UsagePharmaceutical, biotech, regulated industriesPharmaceutical, biotech, regulated industries
Primary FocusLeading validation projects, team coordinationPerforming validation activities, testing

The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.

What are popular job titles related to Computer System Validation Manager jobs in Miami, FL? For Computer System Validation Manager jobs in Miami, FL, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Manager jobs in Miami, FL look for? The top searched job categories for Computer System Validation Manager jobs in Miami, FL are:
What cities near Miami, FL are hiring for Computer System Validation Manager jobs? Cities near Miami, FL with the most Computer System Validation Manager job openings:
Computer System Validation Manager jobs near you
Validation Engineer

Validation Engineer

Aequor Inc

Davie, FL • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Validation Engineer 1

Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to product and process quality, writes qualification protocols for operating systems and records related test results; prepares final reports that identify the results of protocol testing and the conditions of release.

This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all duties listed, and may be required to perform additional, position-specific tasks.

  • Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws.
  • Reviews electrical, mechanical, and software/computer specifications in manufacturer and blue print form, and identifies critical parameters.
  • Writes protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems, or equipment.
  • Assures that protocols are approved through proper channels; writes and revises validation protocols.
  • Executes validation and qualification protocols per related SOPs and assures that acceptance criterion related to validation and qualification protocols are met.
  • Assures that all test data is gathered and recorded in accordance with cGMP requirements.
  • Analyzes data to ascertain if it meets related protocol acceptance criteria; writes deviation reports as required upon failures to meet protocol acceptance criteria.
  • Writes final reports and assures that they are approved through proper channels.
  • Develops and communicates project timelines and status.
  • Complies with all GMP and safety requirements, SOP's and Company policies and procedures. Performs equipment and system qualification periodic reviews.
  • Performs related duties as assigned.

Knowledge of:

  • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
  • Pharmaceutical principles, practices and applications.
  • English usage, spelling, grammar and punctuation.
  • Principles of mathematical and statistical computations.
  • Personal computer operations and Microsoft applications (Word, Access, and Excel).

Skill in:

  • Interpreting software and ladder logic diagrams and flowcharts.
  • Interpreting electrical, and mechanical blue prints and specifications including HVAC systems and. construction plans.
  • Solving practical problems and considering a variety of concrete variables in situations where only limited standardization exists.
  • Communicating clearly and concisely, both orally and in writing.
  • Establishing and maintaining good relationships with those encountered in the course of work.
  • Operating a personal computer.

Physical Requirements and Working Conditions

Incumbents in this class are subject to extended periods of sitting, standing, walking, pushing and pulling, stooping and crouching climbing and walking, vision to monitor, occasional lifting of equipment or materials weighing up to 25 pounds. Incumbents may be exposed to toxic materials, toxic gases, electrical hazards, and dangerous tools and equipment. Work is performed in a manufacturing environment.

Minimum Qualifications:

Bachelor's degree in Engineering or a related field from an accredited college or university and zero (0) to one (1) year of engineering validation experience, preferably in a pharmaceutical environment, or an equivalent combination of training and experience.

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