Top 17 Process engineer Jobs in Greenville, Nc

Engineer III, Validation - Process & Cleaning
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Mid-level
- Office
- Bachelor's degree
Process Engineer
LS Cable & System U S A Inc —Tarboro, NC
- Full-time
- Engineering
- Mid-level
- Quality control
Process Engineering Specialist
Attindas - US —Greenville, NC
- Full-time
- Microsoft Access
- 5 years
- Mid-level
Quick Apply
2d
Korean Bilingual Process Engineer
Cesna Recruitment —Tarboro, NC
- $60,000 - $65,000 a year
- Full-time
- Engineering
- Mid-level
- Quality control
- Health insurance
- Dental insurance
Quick Apply
Manager, Process Engineering
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Management
- Engineering
- Office

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process engineer jobs near greenville, nc

Engineer III, Validation - Process & Cleaning

Thermo Fisher Scientific -
Greenville, NC

Apply Now

Job Details

Full-time

Qualifications

Manufacturing facility experience
Pharmaceutical company experience
Pharmaceutical manufacturing facility experience

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

Discover Impactful Work:

Join Thermo Fisher Scientific and be part of a team delivering life-changing therapies through world-class sterile pharmaceutical manufacturing.

As a Validation Engineer III, you will lead validation activities supporting process and cleaning validation in sterile environments, playing a key role in ensuring compliance, quality, and successful product launches.

This role offers high visibility and cross-functional exposure, working across Operations, Quality, and QC Labs—often acting as a technical lead during tech transfers and validation execution.

A Day in the Life:

~70% desk-based: protocol writing, data analysis, deviation investigations, reporting
~30% on the floor: executing validation in sterile manufacturing environments
Lead validation activities including:
- Process validation
- Cleaning validation
- Equipment qualification (IQ/OQ/PQ)
Support tech transfers and new product introductions
Collaborate cross-functionally with Ops, QC, and Quality teams
Participate in client interactions, audits, and regulatory readiness

What to Expect:

Ownership of complex validation projects
High exposure across site operations and leadership teams
Opportunity to act in a project management capacity
Involvement in audits, deviations, and continuous improvement

Keys to Success:

Education & Experience:

Bachelor’s degree and 4+ years validation experience
Experience in pharmaceutical or biotech manufacturing required
Direct experience in sterile/aseptic pharmaceutical manufacturing highly preferred:
- Aseptic filling
- Sterile processing
- Cleanroom environments

Skills & Expertise:

Strong experience with:
- Process validation
- Cleaning validation
- Equipment qualification (IQ/OQ/PQ)
Proven ability to write and execute validation protocols and reports
Experience with validation documentation and regulatory standards
Exposure to audits, audit responses, or regulatory inspections
Strong problem-solving and deviation investigation skills

Preferred:

Experience in both process and cleaning validation
Background in sterile filling or manufacturing operations
Knowledge of FDA, EMA, and cGMP regulations

Work Environment & Requirements:

Onsite role in Greenville, NC
Monday–Friday schedule with flexibility as needed
Cleanroom and production floor exposure required

Why Join Us:

Work on cutting-edge sterile pharmaceutical programs
Gain broad cross-functional exposure across the site
Be part of high-impact tech transfers and product launches
Clear path to senior and leadership roles

Apply Now

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process engineer jobs in greenville, nc

Engineer III, Validation - Process & Cleaning

Process Engineer

Process Engineering Specialist

Korean Bilingual Process Engineer

Manager, Process Engineering