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Process Engineer Jobs in Erlanger, KY (NOW HIRING)

Process Engineer II (MSAT) - Dayshift

Blue Ash, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com The Process Engineer II, will handle execution of technical aspects of product and/or process technology transfer to the site through successful ...

Process Engineer III - Packaging

West Chester, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com Position Summary The Process Engineer III - Packaging is a technical leader responsible for validated packaging processes supporting combination ...

Process Engineer II (MSAT) - Dayshift

Blue Ash, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com The Process Engineer II, will handle execution of technical aspects of product and/or process technology transfer to the site through successful ...

Process Engineer III - Packaging

West Chester, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com Position Summary The Process Engineer III - Packaging is a technical leader responsible for validated packaging processes supporting combination ...

Process Engineer III - Packaging

West Chester, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com Position Summary The Process Engineer III - Packaging is a technical leader responsible for validated packaging processes supporting combination ...

Process Engineer II (MSAT) - Dayshift

Blue Ash, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com The Process Engineer II, will handle execution of technical aspects of product and/or process technology transfer to the site through successful ...

Process Engineer III- Inspection

West Chester, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com Position Summary The Process Engineer III - Inspection is a mid-level technical leader responsible for the reliability, performance, validation ...

Process Engineer III- Inspection

West Chester, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com Position Summary The Process Engineer III - Inspection is a mid-level technical leader responsible for the reliability, performance, validation ...

Process Engineer III- Inspection

West Chester, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

For more information, please visit www.resilience.com Position Summary The Process Engineer III - Inspection is a mid-level technical leader responsible for the reliability, performance, validation ...

Process

Hamilton, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Process Engineers provide support for all phases of new capital projects to include capital project scope development, Process Flow Diagram's, equipment and instrumentation specifications, equipment ...

Showing results 21-40

Process Engineer information

See Erlanger, KY salary details

$48.8K

$90.7K

$140.5K

How much do process engineer jobs pay per year?

As of Aug 16, 2026, the average yearly pay for process engineer in Erlanger, KY is $90,725.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $101,600.00 per year, depending on experience, location, and employer.

What is the work of a process engineer?

A process engineer designs, develops, and optimizes manufacturing processes to improve efficiency, quality, and safety. They analyze production workflows, troubleshoot issues, and implement improvements using tools like process flow diagrams and statistical analysis. Strong problem-solving skills and knowledge of industry standards are essential for this role.

What are some common challenges process engineers face when implementing process improvements, and how can they overcome them?

Process Engineers often encounter challenges such as resistance to change from team members, integrating new technologies with existing systems, and ensuring process changes meet regulatory standards. Overcoming these obstacles typically involves clear communication, involving stakeholders early in the process, thorough documentation, and piloting changes before full-scale implementation. Building strong cross-functional relationships and continuously gathering feedback also help ensure that improvements are effective and sustainable.

What is a process engineer?

Process Engineers are professionals who design, implement, and optimize industrial processes to improve efficiency, quality, and safety in manufacturing or production environments. They analyze workflows, troubleshoot process issues, and develop solutions to enhance productivity and reduce costs. Process Engineers often work in industries such as chemicals, pharmaceuticals, food and beverage, and energy, ensuring processes are compliant with environmental and safety regulations. Their work is vital for maintaining smooth operations and achieving organizational goals.

What jobs do process engineers do?

Process engineers design, develop, and optimize manufacturing processes to improve efficiency, safety, and quality. They analyze production data, troubleshoot issues, and implement process improvements using tools like process flow diagrams and statistical analysis. Their work often involves collaboration with production teams and requires knowledge of engineering principles and industry standards.

What are the key skills and qualifications needed to thrive as a process engineer, and why are they important?

To thrive as a Process Engineer, you need a solid background in chemical, mechanical, or industrial engineering, often supported by a relevant bachelor's degree and understanding of process optimization principles. Familiarity with process simulation software (such as Aspen Plus or AutoCAD), Six Sigma methodologies, and quality management systems is typically required. Strong analytical thinking, problem-solving abilities, and effective communication skills set candidates apart in this role. These skills and qualifications are essential to improve efficiency, ensure safety, and drive continuous improvement in industrial and manufacturing processes.

What is the difference between Process Engineer vs Manufacturing Engineer?

AspectProcess EngineerManufacturing Engineer
CredentialsBachelor's in Engineering, certifications like Six SigmaBachelor's in Engineering, certifications like Lean Manufacturing
Work EnvironmentDesigning and optimizing processes, R&D settingsOverseeing production lines, factory floors
Industry UsageManufacturing, chemical, aerospaceAutomotive, electronics, consumer goods

Process Engineers focus on designing and improving manufacturing processes, often working in R&D or engineering departments. Manufacturing Engineers concentrate on implementing and managing production on the factory floor. Both roles require similar technical skills and certifications but differ mainly in their scope and work environment.

What are the most commonly searched types of Process Engineer jobs in Erlanger, KY?

The most popular types of Process Engineer jobs in Erlanger, KY are:

What cities near Erlanger, KY are hiring for Process Engineer jobs?

Cities near Erlanger, KY with the most Process Engineer job openings:

Infographic showing various Process Engineer job openings in Erlanger, KY as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% In-person job distribution, with an average salary of $90,725 per year, or $43.6 per hour.

Manufacturing Process Engineer

Thermo Fisher Scientific

Cincinnati, OH

$70K - $94K/yr

Full-time

Re-posted 26 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 426 frontline employees who took The Breakroom Quiz

199th of 540 rated manufacturers


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Join our team as a Manufacturing Sciences Scientist II, where you'll contribute to ensuring consistent production of therapeutic and diagnostic products. As part of our Manufacturing Sciences team, you'll work at the intersection of research and production, supporting process optimization, technology transfer, and continuous improvement initiatives. You'll collaborate with cross-functional teams to resolve technical challenges and ensure robust, scalable manufacturing processes that meet quality standards.

As a Manufacturing Scientist II, you will lead and/or implement activities for the development of new and established manufacturing processes of solids, liquids, and semi-solid dosage forms. Project management skills will be applied to implement the scaling up manufacturing processes, supporting new product validations and post approval qualifications activities. This will require the writing, approval, and routing documents within a manufacturing setting. 

You will be the primary technical representative on client projects and will work closely work with internal and external project teams of analytical, quality, and project management representatives. Supporting process development and commercial activities will be required. Leads technical/scientific project activities and discussions to lead strategies and technical solutions that meet client needs and expectations. 

Investigates, creates, and validates new scientific and equipment methodologies for a diverse scope of projects.  Using experimental design, established formulation processes for the following phases of product scale-up, registration, and validation.  

Creates processes and equipment design for clinical, scale up, and/or registration batches, including technology transfer of projects to and from clients. Leads problem solving activities as necessary with independent judgement.  Makes decisions that require choosing between multiple options or may develop new options to resolve moderately complex problems. 

REQUIREMENTS:

Bachelor's Degree plus 2 years of experience in GMP manufacturing, process development, or related technical role

•Preferred Fields of Study: Bachelor's degree in chemical engineering (or other engineering field), chemistry, pharmacy, or other related science or technical field is required. 

• Strong understanding of cGMP requirements, regulatory compliance, and quality systems

• Experience with process validation, technology transfer, and scale-up activities

• Strong project management and documentation skills

• Excellent written and verbal communication abilities

• Ability to work independently and collaboratively in a dynamic environment

• Demonstrated problem-solving and troubleshooting capabilities

• Proficient with Microsoft Office Suite and relevant manufacturing/quality systems

• Experience with risk assessment and root cause analysis

• Ability to train and support team members

• May require occasional weekend/off-hours support

• Must be able to wear required PPE and work in controlled environments

How will you get here?

Education

Bachelor's degree in chemical engineering (or other engineering field), chemistry, pharmacy, or other related science or technical field is required.

Experience

  • Minimum of one (1) to three (3) years of experience in a manufacturing environment. Experience in product or process development, including scale-up and technology transfer processes for both immediate and controlled release dosage forms preferred.

  • Project Management experience with a minimum (1) year of experience.

Knowledge, Skills, Abilities

  • Understanding of Good Manufacturing Practices (GMP) and regulatory compliance.

  • Lead projects of moderate to high complexity in scope and compliance-related challenges to implementing processes to meet changing regulations.

  • Proficiency using Microsoft (MS) Office applications.

  • Good critical and logical thinking skills. Effective written, interpersonal, and presentation skills, including leading technical discussions with internal and external clients.

  • Self-starter, mature, independent, and detailed oriented.

  • Ability to work in a fast-paced, results oriented, and structured environment.

  • Experience leading projects related to process development including scale-up production activities.

  • Effective time management, multi-tasking and prioritization skills to effectively run multiple projects.

  • Lead by example.

  • Courages and assumes challenges in a risk based approaches.

  • Transparent and knowledgeable in presenting project updates daily.

  • Diligent in team meetings and discussions.

  • Collaborate across multiple departments to reach goals and objectives.

  • Inclusive with communication styles and ideas.

  • Conscientious to fellow peers with work load requirements.

  • Coordinate and lead weekly meetings with customers.

  • Fast and focused execution of tasks will be required at time.

  • Build helpful ideas to increase production efficiencies.

  • Technical skill information transferred to supporting departments.

  • Participate and support audit participation and interaction for regulatory agencies.

  • Develop and transform learning to peers with technical and mechanical result oriented aptitudes.

  • Written communication skills expected and presentation will be expected.

Physical Requirements:

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office and manufacturing locations; ability to stand, walk, stoop, kneel, crouch periodically, manipulation (lift, carry, move) of light to medium weights of 10-35 pounds; arm, hand and finger dexterity, including ability to grasp and type for periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

Must be legally authorized to work in the United States without sponsorship

Relocation assistance is not provided 

Must be able to pass a comprehensive background check, including a drug screening 


What Thermo Fisher Scientific employees say

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