Top 31 Engineer iii, computer systems validation Jobs in Greenville, Nc

Engineer II, Computer Systems Validation
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Engineering
- Mid-level
- Office
Dosimetrist
UHealthSolutions —North Carolina
- $130,000 - $145,000 a year
- 8 hour shift
- Background check
- Customer service
- Computer literacy
- Health insurance
- Dental insurance
Quick Apply
Engineer III, Computer Systems Validation
Thermo Fisher Scientific —Greenville, NC
- Extended hours
- Engineering
- Office
- Microsoft Office
Quality Assurance Manager
Valicy —Greenville, NC
- Computer Science
- Analysis skills
- Mentoring
Quick Apply
Staff QA Engineer
Thermo Fisher Scientific —Greenville, NC
- Full-time
- 6 years
- Office
- Analysis skills
Engineer III, Validation - Process & Cleaning
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Mid-level
- Office
- Bachelor's degree
Sr QA Specialist - Quality Risk Management
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Background check
- 6 years
- Pass drug screening
- Paid parental leave
- Paid holidays
Robot Service Technician – Full Time/Contract
Avride —Greenville, NC
- Full-time
- Clean driving record
- Mid-level
- Ability to lift 50 pounds
- Commuter assistance
- Disability insurance
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Validation Engineer
Validation & Engineering Group, Inc —Greenville, NC
- Full-time
- Engineering
- Mid-level
- Organizational skills
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MES developer - Rockwell, Factorytalk
Cognizant —Greenville, NC
- $95,000 - $130,000 a year
- Full-time
- Hybrid work
- Computer Science
- Mid-level
- Office
- Health savings account
- AD&D insurance
Project Controls Manager - Project Farma
PerkinElmer —Greenville, NC
- $94,000 - $203,000 a year
- Full-time
- Military
- Master's degree
- Travel
Lead Formulation Technician (12hr days or 12hr nights, 2-2-3 rotation)
Thermo Fisher Scientific —Greenville, NC
- 12 hour shift
- Ability to walk for extended periods
- Computer literacy
- Mid-level

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Engineer II, Computer Systems Validation

Thermo Fisher Scientific -
Greenville, NC

Apply Now

Job Details

Full-time

Qualifications

Content creation for technical audiences
Engineering development testing
Technical documentation
Engineering
Technical writing experience within manufacturing
Gap analysis
GMP
Mid-level
Analysis skills
Bachelor's degree in engineering
Production validation processes
Change management for system development
Quality risk management
System testing
Requirements analysis
Compliance documentation
Quality compliance management
Automated systems
Regulatory/legal compliance standards in production
Supervisory control and data acquisition (SCADA)
Chemistry
Collaboration with manufacturing teams
Operational excellence initiatives
Productivity software
Test validation method
2 years
Production documentation
Continuous process improvement (CPI)
Communication skills
Bachelor's degree in chemistry

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges.

About the Business

Join our Pharma Services Group (PSG)—a global leader providing integrated drug development and manufacturing solutions to pharmaceutical and biotech companies. Our Greenville, North Carolina site specializes in sterile and oral solid dose (OSD) manufacturing, supported by advanced technologies and a highly collaborative team environment.

Discover Impactful Work

As an Engineer II, Computer Systems Validation (CSV), you will support validation activities tied to automation systems, manufacturing equipment, and computerized systems across the site. This role is primarily focused on change management and validation of existing commercial manufacturing systems, ensuring compliance and operational readiness.

You will partner closely with automation, manufacturing, and quality teams to evaluate system changes, determine validation requirements, and execute qualification activities that maintain regulatory compliance and product quality.

A Day in the Life

Evaluate changes to existing manufacturing systems, equipment, and related databases
Support change management activities for commercial production lines
Author and execute validation documentation including IQ/OQ/PQ protocols and qualification plans
Perform risk assessments, validation assessments, and gap analyses to determine testing requirements
Collaborate with automation and engineering teams to qualify system changes
Support validation of automation and control systems (PLC, SCADA, DCS, DeltaV, etc.)
Ensure compliance with cGMP, FDA, and industry standards
Maintain accurate and compliant validation documentation
Participate in continuous improvement and operational excellence initiatives

Work Schedule & Environment

Standard schedule: Monday–Friday, 8:00 AM – 5:00 PM
Flexibility required to support off-hours work during shutdowns or system availability windows
Fully onsite role in Greenville, NC
Work may occur in manufacturing or controlled environments as needed

Keys to Success

Education (Required)

Bachelor’s degree in Engineering, Life Sciences, Chemistry, or related technical field

Equivalency:
Equivalent combinations of education, training, and relevant experience may be considered in place of a degree

Experience (Preferred, Not Required)

Approximately 2 years of experience in validation, CSV, or a GMP-regulated environment
Internship, co-op, or academic project experience in validation, automation, or regulated industries will also be considered

Knowledge, Skills, Abilities

Foundational understanding of cGMP and regulated environments
Exposure to Computer Systems Validation (CSV), CQV, or automation validation
Familiarity with automation/control systems (e.g., PLCs, SCADA, DCS, DeltaV, Allen-Bradley)
Ability to support development of validation protocols (IQ/OQ/PQ)
Strong technical writing and documentation skills
Basic understanding of risk assessments and gap analysis
Strong analytical and problem-solving skills
Effective communication and collaboration skills
Ability to manage multiple tasks in a fast-paced environment
Proficiency with Microsoft Office tools

Preferred Qualifications

Experience working with automation engineers or manufacturing systems
Exposure to change management processes in regulated environments
Familiarity with quality systems and validation lifecycle documentation

Competencies

Detail-oriented
Collaborative team player
Adaptable and flexible
Strong communicator
Quality and compliance focused

Additional Information

Role is primarily focused on Computer Systems Validation (CSV), with potential exposure to capital projects as business needs evolve
This position is not expected to independently lead full-scale capital validation projects at this level
Designed to support growth and development with guidance from experienced team members

Apply Now

Refine Your Search

engineer iii, computer systems validation jobs in greenville, nc

Engineer II, Computer Systems Validation

Dosimetrist

Engineer III, Computer Systems Validation

Quality Assurance Manager

Staff QA Engineer

Engineer III, Validation - Process & Cleaning

Sr QA Specialist - Quality Risk Management

Robot Service Technician – Full Time/Contract

Validation Engineer

MES developer - Rockwell, Factorytalk

Project Controls Manager - Project Farma

Lead Formulation Technician (12hr days or 12hr nights, 2-2-3 rotation)

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