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Process Engineer Jobs in Gainesville, FL (NOW HIRING)

JLL

Automation Engineer

Gainesville, FL · On-site

Automation Engineer - JLL What this job involves: We are seeking an experienced Automation Engineer ... Conduct root cause analysis, implement process improvements, and drive continuous improvement ...

Jacobs Management Group

Packaging Engineer

Alachua, FL · On-site

$65K - $80K/yr

If you want your engineering work to carry real clinical weight, this is where to do it. Why you ... Comfortable applying process validation methodology (IQ, OQ, PQ) and statistical tools (Gage R&R ...

Advita Ortho

Design Engineer, Packaging

Gainesville, FL · On-site

$122K/yr

Design Engineer, Packaging Department: Manufacturing Engineering Employment Type: Full Time ... Includes qualification/testing of packaging configurations and process validation. Key ...

University of Florida

Engineer II

Gainesville, FL · On-site

$68K - $75K/yr

Engineer II Job no: 540773 Work type: Staff Full-Time Location: Main Campus (Gainesville, FL ... Microelectronics and semiconductor fabrication knowledge Hands-on processing, metrology ...

Philips

Senior DevOps Engineer

Gainesville, FL · On-site

$115K - $183K/yr

... Engineer - Gainesville, FL Join our Disease Management Systems (DMS) team as a Software DevOps ... automated build and deployment processes. * Monitor system health, collect and analyze ...

New

Philips

Senior DevOps Engineer

Gainesville, FL · On-site

$115K - $183K/yr

... Engineer - Gainesville, FL Join our Disease Management Systems (DMS) team as a Software DevOps ... automated build and deployment processes. * Monitor system health, collect and analyze ...

New

Evergen

Operations Engineer 2

Alachua, FL · On-site

$75K - $95K/yr

Provides manufacturing engineering support and recommendations for direct projects in assigned ... Leads the development and improvement of the manufacturing process for existing and new products

Baker Water, LLC

Project Engineer

Gainesville, FL · On-site

Summary As a Project Engineer, you'll support the planning, coordination, and execution of large ... process may make their requests known by emailing hrtech@sharedservices.cc or calling 1-513-539 ...

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All JobsProcess Engineer JobsProcess Engineer Jobs in Gainesville, FL

Process Engineer information

See Gainesville, FL salary details

$44.8K

$83.4K

$129.1K

How much do process engineer jobs pay per year?

As of Aug 9, 2026, the average yearly pay for process engineer in Gainesville, FL is $83,368.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,500.00 and $93,300.00 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.

More about Process Engineer jobs
What are the most commonly searched types of Process Engineer jobs in Gainesville, FL? The most popular types of Process Engineer jobs in Gainesville, FL are:
What job categories do people searching Process Engineer jobs in Gainesville, FL look for? The top searched job categories for Process Engineer jobs in Gainesville, FL are:
What cities near Gainesville, FL are hiring for Process Engineer jobs? Cities near Gainesville, FL with the most Process Engineer job openings:
Process Engineer jobs near you
Infographic showing various Process Engineer job openings in Gainesville, FL as of July 2026, with employment types broken down into 87% Full Time, 3% Part Time, 7% Temporary, and 3% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $83,368 per year, or $40.1 per hour.

Senior Quality Engineer, Validation

Advita Ortho

Gainesville, FL • On-site

$79K - $108K/yr

Full-time

Posted 3 days ago

New

Job description

Senior Quality Engineer, Validation
Department: Quality
Employment Type: Full Time
Location: Gainesville, FL
Reporting To: Sr Manager Quality Engineering
Description
This position offers flexibility to align with the candidate's experience level and can be structure as a Senior Validation Engineer role for those with advanced expertise.
The Validation Engineer provides cross-functional support in V&V development, planning and execution while maintaining corporate engineering and quality systems best practices, policies and procedures. The Validation Engineer is results oriented and has the knowledge and confidence in the areas of Quality Assurance and validation/verification (V&V).
Key Responsibilities
  • Provide focused, technical, hands-on engineering assistance regarding V&V requirements of medical device processes, materials, equipment and methods including project management, process design, document generation (IQ, OQ, PQ, SOPs, WIs and ETSs), critical process parameter development, protocol execution and summary reports.
  • Participates in the development and execution of robust inspection and test methods for V&V feasibility and qualification projects and stand alone studies.
  • Leads or participates in the validation of corporate software packages ensuring adherence to industry requirements.
  • Use statistical techniques, as necessary, to properly design and execute V&V activities.
  • Prepare documentation and execute V&V activities utilizing a risk based approach (pFMEA, FMEA, etc.) and Good Engineering Practices (GEPs) ensuring compliance to medical device industry regulations.
  • Coordinate personnel training, protocol and process documentation/record retrieval, as necessary, supporting timely execution and closure of all corporate V&V activities.
  • Maintain corporate validation process auditing program ensuring timely completion of auditing activities.
  • Maintain V&V planning (Validation Project Dashboard) documenting progress towards completion of corporate V&V initiatives in preparation for monthly update meetings.
  • Lead the identification, maintenance, development and enhancement of corporate systems, processes and standards.
  • Identify, analyze and correct internal and external manufacturing deviations and/or anomalies related to V&V activities ensuring optimization of production processes.
  • Successfully contribute to cross-functional project teams in all areas of device cleanliness and manufacturing V&V work such as material testing, specification development, process capability studies, research, and investigation and process/test documentation.
  • Identify and communicate significant quality and compliance concerns to the Mgr. Validations, QA and associated project team leaders early in the V&V development phase.
  • Informs Regulatory Affairs of validation projects that may require further reporting/scrutiny (e.g. PMA devices).
  • Participate in the review and qualification of external supply chain V&V activities.
  • Take primary responsibility for company-wide validation related Corrective and Preventive Actions that may result from internal/external non-conformances, recalls and/or field actions.
  • Define and lead third party, customer and regulatory audits as they pertain to validations.

Skills Knowledge and Expertise
Education:
  • Bachelor's Degree from an accredited institution required; Master's Degree preferred

Experience:
  • Advanced level of technical software proficiency
  • Excellent Quality System knowledge required
  • Strong time management and project management skills are necessary.
  • Experience writing IQ/OQ/PQ V&V protocols.
  • Working knowledge of principles, concepts and practices of process V&V activities, Risk Management, FDA and ISO Regulations.
  • General understanding of sterilization and related analytical testing is a plus.
    Must be able to work independently and in a team environment.

Functional/Technical Knowledge, Skills and Abilities Required:
  • Statistical expertise in areas such as process capability, process assurance and sampling
  • Expertise in Microsoft Office products
  • Ability to work effectively in a team environment
  • ASQ Certifications preferred
  • Advanced level of technical software proficiency
  • Working knowledge of statistical analysis and sampling plans.
  • Excellent communication (written and verbal) skills.
  • Excellent organization skills.

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