Top 6 Quality engineer medical device Jobs in Tarboro, Nc

Quality Engineer, QA Validation
Thermo Fisher Scientific —Greenville, NC
- Full-time
- 5 years
- Office
- Analysis skills
Staff QA Engineer
Thermo Fisher Scientific —Greenville, NC
- Full-time
- 6 years
- Office
- Analysis skills
Quality Engineer
Philip Morris International U.S. —Wilson, NC
- $80,000 - $100,000 a year
- Full-time
- Engineering
- English
- 3 years
- Commuter assistance
- Health insurance
Validation Engineer
Validation & Engineering Group, Inc —Greenville, NC
- Full-time
- Engineering
- Mid-level
- Organizational skills
Quick Apply
Senior Controls Engineer
Ossid LLC —Battleboro, NC
- Full-time
- 7 years
- Bachelor of Science
- Engineering
- Wellness program
- Disability insurance
Fixture Designer
Quest Global —Wilson, NC
- $72,000 - $75,000 a year
- Full-time
- 6 years
- Bachelor of Science
- Travel
- Disability insurance
- Health insurance
Quick Apply

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Staff QA Engineer
Thermo Fisher Scientific —Greenville, NC
Preferred Fields of Study: Engineering, Life Sciences, Chemistry, Biology, or related technical/scientific field. Travel up to 25% as required.
Quality Engineer, QA Validation
Thermo Fisher Scientific —Greenville, NC
Preferred Fields of Study: Engineering, Science, Biotechnology, or related technical field. Your expertise will be vital in maintaining compliance, driving…

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quality engineer medical device jobs near tarboro, nc

Quality Engineer, QA Validation

Thermo Fisher Scientific -
Greenville, NC

Apply Now

Job Details

Full-time

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
Pharmaceutical company experience
Project management experience in healthcare
Compliance documentation
Mentoring
Biomedical regulatory compliance
Industrial equipment
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 plus 6 years of experience, or Bachelor's Degree 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

Refine Your Search

quality engineer medical device jobs in tarboro, nc

Quality Engineer, QA Validation

Staff QA Engineer

Quality Engineer

Validation Engineer

Senior Controls Engineer

Fixture Designer

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alert for quality engineer medical device in tarboro, nc

Explore jobs in more locations

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:

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