Top 139 Validation Jobs in Greenville, Nc

Validation Engineer III - OSD/Packaging/AVI
Thermo Fisher Scientific —Greenville, NC
- Extended hours
- Engineering
- Office
- 3 years
7d
Validation Engineer
Validation & Engineering Group, Inc —Greenville, NC
- Full-time
- Engineering
- Mid-level
- Organizational skills
Quick Apply
QA Automation Engineer
Valicy —Greenville, NC
- Senior level
- Communication skills
- Python
Quick Apply
Engineer II, Validation - AVI
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Engineering
- Office
- In-person
Engineer III, Validation - Process & Cleaning
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Mid-level
- Office
- Bachelor's degree
Quality Assurance Manager
Valicy —Greenville, NC
- Computer Science
- Analysis skills
- Mentoring
Quick Apply
Engineer III, Computer Systems Validation
Thermo Fisher Scientific —Greenville, NC
- Extended hours
- Engineering
- Office
- Microsoft Office
R&D/Mfg Scientist II-Reviewer
Thermo Fisher Scientific —Greenville, NC
- Full-time
- English
- Mid-level
- 3 years
11d
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
Quick Apply
MSAT Scientist (Technology Transfer)
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Microsoft Excel
- Bachelor of Science
- Office
12d
Manager - CAPA Effectiveness
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Office
- 3 years
- Analysis skills
Project Manager
Catalent —Greenville, NC
- Email
- Microsoft Excel
- Mid-level
- High school diploma or GED
- Paid holidays
- Paid time off
MSAT Scientist II (Technology Transfer)
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Microsoft Excel
- Bachelor of Science
- Mid-level
12d
Electrical SME - Field Consultant
Cumming Group —North Carolina
- $104,600.00 - $139,466.68 a year
- Full-time
- 6 years
- Construction site
- Bachelor of Science
- Paid holidays
- Disability insurance
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
Nuclear Medicine Technologist
UHealthSolutions —North Carolina
- $37 - $42 an hour
- Full-time
- Customer service
- BLS Certification
- English
- Health insurance
- Dental insurance
Quick Apply
Accounts Payable Specialist
Valicy —Greenville, NC
- Full-time
- Oracle
- Mid-level
- Office
Quick Apply
Quality Engineer
LS Cable & System U S A Inc —Tarboro, NC
- Full-time
- Laboratory experience
- Analysis skills
- Electrical Engineering
11d
Manager, IS Vendor & Contract
ECU Health —Greenville, NC
- $96,824.00 - $141,123.84 a year
- Full-time
- Hybrid work
- Office
- 3 years
- Analysis skills
1d
Senior Quality Project Lead – Customer Quality
Thermo Fisher Scientific —Greenville, NC
- Full-time
- 5 years
- Engineering
- Office

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Validation Engineer III - OSD/Packaging/AVI

Thermo Fisher Scientific -
Greenville, NC

Apply Now

Job Details

Full-time
7 days ago

Qualifications

Quality control samples
Content creation for technical audiences
Data analysis reporting
Personal protective equipment (PPE) use
Technical documentation
Engineering
Continuous improvement standards implementation
Technical writing experience within manufacturing
GMP
3 years
Data summary reports
Manufacturing facility experience
Bachelor's degree in engineering
Production validation processes
Pharmaceutical company experience
Scientific protocols
Packaging
Compliance documentation
Visual inspection as testing technique
Regulatory/legal compliance standards in production
Cleanroom experience
Chemistry
Collaboration with manufacturing teams
Document quality checks
Operational excellence initiatives
Productivity software
Engineering functional testing
Manufacturing
Lean management
Senior level

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

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, like protecting the environment, making sure our food is safe, and helping find cures for cancer.

At our Greenville, North Carolina site, you'll join a highly collaborative Validation Engineering team supporting pharmaceutical manufacturing operations. Our team plays a critical role in ensuring manufacturing processes are validated, compliant, and capable of consistently producing high-quality medicines that improve lives around the world.

Discover Impactful Work

As a Validation Engineer III, you will support manufacturing process validation activities focused primarily on Oral Solid Dose (OSD) continuous manufacturing and pharmaceutical packaging operations. You'll lead validation efforts from protocol development through execution and final reporting while partnering with Manufacturing, Engineering, Quality, and Technical Operations teams.

This role offers an excellent balance of technical documentation and hands-on manufacturing support, allowing you to contribute directly to product launches, process improvements, and regulatory compliance. In addition to OSD process and packaging validation, you'll have opportunities to support Automated Visual Inspection (AVI) validation activities as business needs require.

A Day in the Life

This position offers approximately:

70% desk-based work
- Write validation protocols and supporting documentation
- Perform data analysis and calculations
- Prepare validation summary reports
- Conduct data review and documentation review
- Support investigation and technical problem solving
30% manufacturing floor execution
- Execute manufacturing process validation protocols
- Perform packaging process validation activities
- Collect validation samples and process data
- Partner with Manufacturing and Quality during validation campaigns
- Support Automated Visual Inspection (AVI) validation activities when needed

Key Responsibilities

Lead manufacturing process validation activities for Oral Solid Dose (OSD) pharmaceutical products.
Develop, execute, and document validation protocols, including IQ, OQ, and PQ.
Perform packaging process validation for commercial pharmaceutical manufacturing.
Analyze validation data and prepare technical reports that support regulatory compliance.
Support cleaning validation activities as part of overall manufacturing process qualification.
Collaborate with Manufacturing, Engineering, Quality, and Technical Operations teams to execute validation projects.
Participate in peer review of validation documentation and data.
Support Automated Visual Inspection (AVI) validation activities as assigned.
Contribute to continuous improvement initiatives that enhance manufacturing performance and compliance.
Support internal audits, customer audits, and regulatory inspections.

Keys to Success

Education

Bachelor's degree in Engineering, Life Sciences, Chemistry, or another technical discipline.
Advanced degree preferred.

Experience

Bachelor's degree with 5+ years of validation experience, or an advanced degree with 3+ years of validation experience within pharmaceutical, biotechnology, or another regulated manufacturing environment.
Experience developing and executing validation protocols in GMP manufacturing.
Experience with IQ/OQ/PQ documentation and execution.

Preferred Experience

Candidates with the following experience will be especially successful in this role:

Oral Solid Dose (OSD) manufacturing process validation
Continuous Manufacturing (CM)
Packaging process validation (preferred over equipment-only validation)
Automated Visual Inspection (AVI)
Sterile packaging validation
Cross-functional collaboration within pharmaceutical manufacturing

Knowledge, Skills & Abilities

Strong knowledge of FDA cGMP regulations and pharmaceutical manufacturing practices.
Experience with manufacturing process validation, equipment qualification, utilities, cleaning processes, and computer systems.
Strong technical writing and documentation skills.
Experience performing validation data analysis and interpretation.
Excellent analytical and problem-solving skills.
Strong communication and collaboration skills with cross-functional teams.
Proficiency with Microsoft Office and validation documentation systems.
Experience supporting regulatory inspections and customer audits is preferred.
Knowledge of Lean Manufacturing or continuous improvement methodologies is a plus.
Ability to work in cleanroom and manufacturing environments.
Flexibility to occasionally support extended hours during validation campaigns.
Occasional travel (up to 25%) may be required to support Factory Acceptance Testing (FAT) or other business needs.

Why Join Us?

At Thermo Fisher Scientific, your work directly impacts patients around the world. You'll collaborate with talented colleagues, work on cutting-edge pharmaceutical manufacturing technologies, and gain experience supporting innovative Oral Solid Dose manufacturing, packaging, and validation programs. We invest in our people through professional development, challenging projects, and opportunities to grow your career while making a meaningful difference.

Apply Now

Refine Your Search

validation jobs in greenville, nc

Validation Engineer III - OSD/Packaging/AVI

Validation Engineer

QA Automation Engineer

Engineer II, Validation - AVI

Engineer III, Validation - Process & Cleaning

Quality Assurance Manager

Engineer III, Computer Systems Validation

R&D/Mfg Scientist II-Reviewer

Robot Service Technician – Full Time/Contract

MSAT Scientist (Technology Transfer)

Manager - CAPA Effectiveness

Project Manager

MSAT Scientist II (Technology Transfer)

Electrical SME - Field Consultant

Dosimetrist

Nuclear Medicine Technologist

Accounts Payable Specialist

Quality Engineer

Manager, IS Vendor & Contract

Senior Quality Project Lead – Customer Quality

I want to receive the latest job alert for validation in greenville, nc

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