Top 97 Quality engineering Jobs in Greenville, Nc

Quality Engineer, QA Validation
Thermo Fisher Scientific —Greenville, NC
- Full-time
- 5 years
- Office
- Analysis skills
14d
Quality Assurance Supervisor
LS Cable & System U S A Inc —Tarboro, NC
- Full-time
- 5 years
- Engineering
- Supervising experience
Senior Project Engineer
Perdue Farms, Inc. —North Carolina
- $114,000 - $170,000 a year
- Weekends as needed
- Remote
- 7 years
- Travel
- Mentoring
- Paid jury duty
- AD&D insurance
Quick Apply
Engineer II Manufacturing Process Engineering
Thermo Fisher Scientific —Greenville, NC
- Overtime
- Engineering
- Laboratory experience
- Mid-level
4d
Quality Specialist II - Complaints
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Ability to walk for extended periods
- Mid-level
- Office
3d
Quality Assurance Manager
Valicy —Greenville, NC
- Computer Science
- Analysis skills
- Mentoring
Quick Apply
Process Engineering Specialist
Attindas - US —Greenville, NC
- Full-time
- Microsoft Access
- 5 years
- Mid-level
Quick Apply
Aerospace Quality Inspector
Trigo Group —Greenville, NC
- $36 - $41 an hour
- Extended hours
- Microsoft Excel
- Microsoft Outlook
- Writing skills
- Travel reimbursement
- Mileage reimbursement
Manufacturing Scientist II
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Microsoft Excel
- Bachelor of Science
- Mid-level
Aerospace Quality Inspector
Trigo ADR Americas —Greenville, NC
- $36 - $41 an hour
- Extended hours
- Microsoft Excel
- Microsoft Outlook
- Writing skills
- Travel reimbursement
- Mileage reimbursement
Manager, Document Control - Quality Systems & Compliance
Thermo Fisher Scientific —Greenville, NC
- Full-time
- 6 years
- Office
- Master's degree
3d
Assistant Engineer - Equipment
Boviet Solar Cell Technology North Carolina LLC —Greenville, NC
- Electrical Engineering
- Entry level
- Under 1 year
Quick Apply
10d
Engineer II, Validation
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Engineering
- Mid-level
- Analysis skills
3d
Lead QA Technician - Batch Record Review (8hr days, Monday-Friday)
Thermo Fisher Scientific —Greenville, NC
- 8 hour shift
- Mid-level
- Office
- 3 years
3d
Manufacturing Engineer (Early Career)
Global Cellulose Fibers —Vanceboro, NC
- $85,000 - $89,000 a year
- Full-time
- 3 years
- Analysis skills
- Electrical Engineering
- Disability insurance
- Health insurance
14d
Outside Plant Engineer
OUTSOURCE, INC. —Greenville, NC
- Full-time
- Civil engineering
- Customer service
- Mid-level
Quick Apply
Sr. Director, Quality - Site Quality Head (Greenville, NC)
Thermo Fisher Scientific —Greenville, NC
- Full-time
- 11+ years
- Office
- Analysis skills
6d
Quality Assurance and Safety Manager
Oak Ridge Metal Works LLC —Washington, NC
- Full-time
- Engineering
- Analysis skills
- Travel
Quick Apply
Engineer III, Computer Systems Validation
Thermo Fisher Scientific —Greenville, NC
- Extended hours
- Engineering
- Office
- Microsoft Office
Quality Engineer
INFOSYS NOVA HOLDINGS LLC —Kinston, NC
- Mid-level
- 4 years
- Communication skills
Quick Apply

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Quality Engineer, QA Validation

Thermo Fisher Scientific -
Greenville, NC

Apply Now

Job Details

Full-time
14 days ago

Qualifications

Data integrity assurance
GAMP
Content creation for technical audiences
Technical documentation
Pharmaceutical regulatory compliance
Technical writing experience within manufacturing
FDA 21 CFR Part 11
Project management experience in manufacturing
Data summary reports
Manufacturing facility experience
Data integrity and documentation
Production validation processes
Quality risk management
Project management experience in healthcare
Compliance documentation
Mentoring
Biomedical regulatory compliance
Manufacturing
Cross-functional collaboration
Cross-functional communication
Pharmaceutical manufacturing facility experience
Engineering quality assurance

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, 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, 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 or helping find cures for cancer.

DESCRIPTION:

Join our QA Validation team at Thermo Fisher Scientific, where you'll contribute to global healthcare and scientific advancement. As a Staff Validation Engineer, you'll lead validation activities for critical systems, equipment, and processes that enable the development and manufacturing of therapies.

Working in a GMP environment, you'll develop and implement comprehensive validation strategies aligned with regulatory requirements and corporate standards. You'll collaborate with cross-functional teams to ensure the successful qualification of facilities, utilities, manufacturing equipment, and computerized systems throughout their lifecycle.

Your expertise will be vital in maintaining compliance, driving continuous improvement, and serving as a technical subject matter expert during audits and investigations. You'll have opportunities to mentor team members while working on diverse projects ranging from new product introductions to complex system validations.

REQUIREMENTS:

5 or more years of medical device experience
Expert knowledge of cGMP regulations, GAMP 5, 21 CFR Part 11, and international regulatory requirements
Strong experience with validation lifecycle documentation including risk assessments, validation plans, IQ/OQ/PQ protocols, and summary reports
Demonstrated expertise in computerized system validation and data integrity requirements
Experience with manufacturing equipment, utilities, and facility qualification
Proven project management skills and ability to lead multiple concurrent validation projects
Strong analytical and problem-solving capabilities
Excellence in technical writing and documentation
Strong communication and interpersonal skills
Ability to influence and coordinate activities across multiple departments
Proficiency with validation tools and standard office software
Experience mentoring validation staff
Physical ability to work in both office and manufacturing environments

EDUCATION:

Advanced Degree preferred plus 6 years of experience, or bachelor's degree preferred plus 8 years of experience in validation experience in pharmaceutical/biotech manufacturing or related GMP environment
Preferred Fields of Study: Engineering, Science, Biotechnology, or related technical field

Apply Now

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5 or more years of medical device experience

Expert knowledge of cGMP regulations, GAMP 5, 21 CFR Part 11, and international regulatory requirements

Strong experience with validation lifecycle documentation including risk assessments, validation plans, IQ/OQ/PQ protocols, and summary reports

Demonstrated expertise in computerized system validation and data integrity requirements

Experience with manufacturing equipment, utilities, and facility qualification

Proven project management skills and ability to lead multiple concurrent validation projects

Strong analytical and problem-solving capabilities

Excellence in technical writing and documentation

Strong communication and interpersonal skills

Ability to influence and coordinate activities across multiple departments

Proficiency with validation tools and standard office software

Experience mentoring validation staff

Physical ability to work in both office and manufacturing environments

EDUCATION: