Top 8 Validation engineer ii Jobs in Columbus

Packaging Engineer II
cGMP Consulting —New Albany, OH
- $75,000 - $95,000 a year
- Full-time
- Engineering
- Mid-level
- Continuous improvement
- Health insurance
- Dental insurance
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Project Engineer I/II/III - Automation
SEL Engineering Services, Inc. —Lewis Center, OH
- $97,000 - $201,000 a year
- Full-time
- Bachelor of Science
- System design
- Mid-level
- Paid holidays
- Disability insurance
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13d
BESS Engineer II (Remote)
SOLV Energy, LLC —Columbus, OH
- $90,000 - $112,506 a year
- Full-time
- Remote
- Microsoft Excel
- Mid-level
- Travel
- Paid holidays
- Disability insurance
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Validation - Engineer I/II - Project Farma
PerkinElmer —Columbus, OH
- $65,000 - $80,000 a year
- Full-time
- Customer service
- Military
- Data analysis skills
Infrastructure Engineer II - Managed File Transfer
JPMorganChase —Columbus, OH
- Full-time
- Data analysis skills
- Mid-level
- Java
- Health insurance
- Tuition reimbursement
Machine Learning Engineer II
Mimecast —Columbus, OH
- $124,000 - $186,000 a year
- Full-time
- Hybrid work
- Computer Science
- Mid-level
- Office
Engineer II, Molding
ICU Medical, Inc. —Dublin, OH
- Full-time
- 18 years or older
- Mid-level
- Office

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Packaging Engineer II
cGMP Consulting —New Albany, OH
Bachelors’ degree in Engineering, Science, or a related field of study. Collaborate with process experts and production personnel to identify and resolve…
$75,000 - $95,000 a year
Quick Apply
Project Engineer I/II/III - Automation
SEL Engineering Services, Inc. —Lewis Center, OH
Lead in training and assisting customers with the creation, design configuration, validation, installation, commissioning and operation of automation and/or…
$97,000 - $201,000 a year
Quick Apply
13d

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Packaging Engineer II

cGMP Consulting -
New Albany, OH

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Job Details

Full-time
$75,000 - $95,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

Content creation for technical audiences
Technical documentation
Technical writing experience within manufacturing
Manufacturing facility experience
Regulatory/legal compliance standards in production
FDA regulations
Pharmaceutical manufacturing facility experience

Full Job Description

About Us

At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities, equipment, and processes meet regulatory standards, enabling the safe and efficient production of pharmaceuticals.
cGMP Consulting is based in Lake Forest, IL. Our main client locations are Melrose Park, IL, North Chicago, IL, Waukegan, IL and Pleasant Prairie, WI.

Position Summary

cGMP Consulting is seeking a motivated and detail-oriented individual to lead projects, including engineering activities for equipment, utilities, facilities, systems, and processes. This mid-level role offers leadership and responsibility in a dynamic, GMP-compliant manufacturing environment.

The ideal candidate has experience in packaging and will excel in leading cross-functional collaboration, troubleshooting, change management, and protocol completion while demonstrating independence. This candidate should have a strong understand of current Good Manufacturing Practices (cGMP) and FDA regulations and guidelines.

Responsibilities

The essential functions include, but are not limited to the following:

Author specifications and supporting documentation (URS, RA, FS) for new processes, equipment, and/or systems.
Perform activities related to scoping, executing, and managing engineering projects involving facility modifications equipment upgrades, or process improvements.
Lead equipment commissioning testing in collaboration with Engineering for new equipment.
Conduct validation/qualification studies for utility systems, equipment, cleaning, processes, computer systems, and new products. This includes protocol preparation, execution, and final report documentation.
Manage multiple qualification activities while providing deliverable updates and modifications to existing scheduling to support execution activities.
Lead cross-functional team meetings, including preparing agendas and documenting meeting notes. Facilitate follow-up meetings in regard to action items previously identified.
Assist in project forecasting and effectively plan requirements for upcoming tasks.
Program and operate analytical instruments (e.g., temperature/humidity dataloggers) for controlled temperature/humidity chamber qualifications, such as lyophilizers, warehouses, sterilizers, and incubators.
Collaborate with process experts and production personnel to identify and resolve technical challenges.
Provide technical expertise and recommend process improvements.
Draft change controls and deviations to address failures during qualification activities.
Author SOP updates related to CAPA implementation.
Maintain compliance with company policies, training requirements, cGMP standards, and safety protocols.
Utilize Word, Excel, Document Management Systems, and other electronic tools to complete tasks efficiently.
Perform additional tasks or duties as assigned by management.

Requirements

Bachelors’ degree in Engineering, Science, or a related field of study.
2-5 years’ experience in a GMP manufacturing environment, specifically packaging. Must be familiar with regulatory (FDA) requirements.
Expertise in one or more of the following areas: cleaning validation, qualification of aseptic filling or formulation equipment/processes, qualification of component preparation equipment/processes, and packaging.
Advanced critical thinking and technical writing skills.
Strong organizational, communication, and interpersonal skills.

Compensation and Benefits

Expected pay range per year: $75,000-$95,000 USD
Expected benefits include: Medical, Dental, Vision, PTO, 401K

Disclaimer

The duties and responsibilities described are not a comprehensive list and additional tasks may be assigned to the employee from time to time; or the scope of the job may change as necessitated by business demands. All duties and responsibilities are subject to possible modification to reasonably accommodate individuals with disabilities. The requirements listed are the minimum levels of knowledge, skills, or abilities necessary to perform this job successfully. The company is an Equal Opportunity Employer, drug-free workplace, and complies with ADA regulations as applicable.

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Refine Your Search

validation engineer ii jobs in columbus

Packaging Engineer II

Project Engineer I/II/III - Automation

BESS Engineer II (Remote)

Validation - Engineer I/II - Project Farma

Infrastructure Engineer II - Managed File Transfer

Machine Learning Engineer II

Engineer II, Molding

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