Top 18 Process engineer Jobs in Mount Vernon, Oh

Sr Engineer- Process Development (CQV)
Katalyst Healthcares & Life Sciences —Newark, OH
- Contract
- Engineering
- Senior level
- Flexible schedule
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MFG ASEPTIC PROCESS ENGINEER
Kroger Manufacturing —Newark, OH
- Full-time
- 3 years
- Bachelor's degree
- Travel
- Paid holidays
- Health insurance
R&D Process Engineer
Bright Innovation Labs —New Albany, OH
- Full-time
- Background check
- Microsoft Excel
- Pass drug screening
Quick Apply
Senior Scientist
Original Composites and Fibers —Granville, OH
- Full-time
- 5 years
- Doctor of Philosophy
- Travel
- Wellness program
- Health savings account
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Sr. Engineering Manager, Beverage
Novolex —United States
- $145,000 - $165,000 a year
- Full-time
- Engineering
- Flatbed truck
- Travel
- Wellness program
- Paid parental leave
Systems Lead Industrial Engineer – AI & Production System
Pro Search, Inc. —United States
- From $200,000 a year
- Full-time
- Background check
- System design
- Continuous improvement
Quick Apply
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Welder
Mettler Toledo —Columbus, OH
Ability to work effectively with torches, cutters, staplers, hand/pneumatic tools, and hand tools (hammers, torque wrench, crow bars, etc.).
Welder
Mettler Toledo —Columbus, OH
Ability to work effectively with torches, cutters, staplers, hand/pneumatic tools, and hand tools (hammers, torque wrench, crow bars, etc.).

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Process Improvement Engineer II (Columbus)
Victoria's Secret —Reynoldsburg, OH
Design, develop, and maintain dashboards, trackers, and reporting tools using Power BI, SharePoint, Excel, databases, and related systems.
$76,700 - $101,955 a year
Process Engineer
Amsted Rail —Groveport, OH
Two to seven years of experience in manufacturing, industrial engineering, process engineering, operations, or a related role. 2 - 7 years: process engineer.
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process engineer jobs near mount vernon, oh

Sr Engineer- Process Development (CQV)

Katalyst Healthcares & Life Sciences -
Newark, OH

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Job Details

Contract

Benefits

Flexible schedule

Qualifications

Technical documentation
Pharmaceutical regulatory compliance
Labeling
GMP
Manufacturing facility experience
Production validation processes
Commissioning phase involvement
Packaging equipment
FDA regulations

Full Job Description

Job Summary:

We are seeking a highly skilled Sr. Engineer Process Development (CQV) to support automated and semi-automated combination product assembly, labeling, and packaging operations within a GMP Final Drug Product (FDP) manufacturing environment. The role involves leading commissioning, qualification, and validation activities for both new and existing equipment and processes, ensuring compliance with FDA regulations and internal quality standards. The Sr. Engineer will serve as the site's technical expert for automated systems and combination product validation, collaborating closely with Engineering, Quality, and Manufacturing teams.

Roles & Responsibilities:

Lead commissioning, qualification, and validation activities for automated and semi-automated combination product equipment and processes.
Author, review, and execute validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Maintain and manage Master Validation Plans and related documentation to ensure compliance with GMP and FDA regulations.
Serve as the technical SME for automated systems, labeling, and packaging process validation.
Collaborate with cross-functional teams (Engineering, Quality, Manufacturing) to ensure robust and validated systems supporting 24/7 production operations.
Conduct on-site and off-shift validation activities as needed to support continuous manufacturing operations.
Identify process gaps and recommend improvements to optimize validation and operational efficiency.
Support regulatory audits and inspections by providing accurate and complete validation documentation.

Education & Experience:

Bachelor's or Master's degree in Engineering, Life Sciences, or related technical field.
Proven experience in Commissioning, Qualification, and Validation (CQV) within a GMP-regulated manufacturing environment.
Hands-on experience with automated and semi-automated equipment, labeling, and packaging operations.
Strong knowledge of FDA regulations, GMP standards, and internal quality systems.
Experience with validation documentation including Master Validation Plans, IQ/OQ/PQ protocols, and reports.
Familiarity with Kneat software is a plus.
Ability to work flexible schedules, including on-site and off-shift validation activities.

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process engineer jobs in mount vernon, oh

Sr Engineer- Process Development (CQV)

MFG ASEPTIC PROCESS ENGINEER

R&D Process Engineer

Senior Scientist

Sr. Engineering Manager, Beverage

Systems Lead Industrial Engineer – AI & Production System

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I want to receive the latest job alert for process engineer in mount vernon, oh

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