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Process Development Engineer Jobs in Fort Collins, CO

Agilent

Validation Engineer

Frederick, CO · On-site

Execute validation studies in support of engineering, manufacturing, process development, facilities, IT, quality control, and quality assurance. * Manage or support the validation program. Suggests ...

Agilent

Validation Engineer

Frederick, CO

Execute validation studies in support of engineering, manufacturing, process development, facilities, IT, quality control, and quality assurance. * Manage or support the validation program. Suggests ...

Antech Diagnostics

Process Engineer II

Longmont, CO · On-site

$84K - $105K/yr

A Process Engineer II understands appropriate documentation in a regulated environment ... Five to seven (5-7) years prior experience in an R&D or production environment with proven success ...

Ursa Major

Development Technician, Inerts

Berthoud, CO · On-site

$25 - $30/hr

The Inerts Dev Tech will report to the Development Team Lead and work alongside other development ... Working closely with engineering during time critical processes to ensure that the required ...

Ursa Major

Development Technician, Inerts

Berthoud, CO · On-site

$25 - $30/hr

The Inerts Dev Tech will report to the Development Team Lead and work alongside other development ... Working closely with engineering during time critical processes to ensure that the required ...

RESPEC

Water Treatment Process Engineer

Loveland, CO · On-site

$90 - $130/hr

RESPEC seeks a Water Treatment Process Engineer in our Water market sector, located in Colorado ... Flexible Work Schedules * 401(k) & ESOP (with company match up to 4%) * Professional Development ...

New

Opterus

Composites Engineer

Loveland, CO · Hybrid

$90K - $128K/yr

This role bridges engineering and manufacturing, focusing on analysis-driven design, process development, manufacturing tooling development, manufacturability, quality, and continuous improvement ...

Opterus

Composites Engineer

Loveland, CO · On-site

$90K - $128K/yr

This role bridges engineering and manufacturing, focusing on analysis-driven design, process development, manufacturing tooling development, manufacturability, quality, and continuous improvement ...

Worky

Process Automation Engineer

Longmont, CO · On-site

$115 - $134/hr

... software development, business systems improvement, or process automation. * Working, practical ... Experience with SQL, Python, JavaScript, or other scripting/programming languages. * Experience ...

Ursa Major

Senior Manufacturing Engineer

Berthoud, CO · On-site

$105K - $130K/yr

Own and support manufacturing process development and champion industry best practices * Establish and communicate design for manufacturing principles in a collaboration with design engineering ...

Ursa Major

Senior Materials Engineer

Berthoud, CO · On-site

$108K - $135K/yr

The Senior Materials Engineer will provide sustaining support on both production and development ... process development, and discrepancy resolution * Author and maintain materials standards and ...

Industrious Ventures

Senior Materials Engineer

Berthoud, CO · On-site

$108 - $135.80/hr

Senior Materials Engineer The Senior Materials Engineer will provide sustaining support on both ... process development, and discrepancy resolution * Author and maintain materials standards and ...

New

Neotech

Process Engineer I

Longmont, CO · On-site

$85 - $110/hr

Summary:Improves manufacturing processes through work flow improvements and automation. Works ... Pursues training and development opportunities; Strives to continuously build knowledge and skills;

New

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Process Development Engineer information

See Fort Collins, CO salary details

$45K

$100.6K

$151K

How much do process development engineer jobs pay per year?

As of Sep 2, 2026, the average yearly pay for process development engineer in Fort Collins, CO is $100,580.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,700.00 and $117,800.00 per year, depending on experience, location, and employer.

What is a process development engineer?

A process development engineer designs and plans production systems to be cost-effective, safe, and meet quality requirements for their industry. These professionals often work as part of a quality assurance team or a production management department for industrial companies, such as manufacturing or mining businesses. As a process development engineer, your job duties include reviewing the company's current production processes and designing modifications to the current system or creating new systems to increase productivity. Once you have installed or implemented the system, you make sure to test and troubleshoot it to ensure they run properly.

What are the key skills and qualifications needed to thrive as a process development engineer?

To thrive as a Process Development Engineer, you need a solid foundation in engineering principles, process optimization, and problem-solving, typically supported by a degree in chemical, mechanical, or industrial engineering. Familiarity with process simulation software (such as Aspen Plus or MATLAB), Six Sigma methodologies, and relevant industry certifications is often required. Strong analytical thinking, effective communication, and teamwork skills help you excel in cross-functional projects and drive continuous improvement. These skills and qualities are crucial for designing efficient processes, ensuring product quality, and supporting organizational competitiveness.

What are some common challenges faced by process development engineers when scaling up from laboratory to production environments?

One of the main challenges Process Development Engineers encounter is ensuring that processes which work efficiently at a laboratory scale can be reliably and safely replicated in full-scale manufacturing. Differences in equipment size, process dynamics, and raw material variability can lead to unforeseen issues such as inconsistent product quality or unexpected safety hazards. Effective communication and collaboration with both R&D and production teams are essential to troubleshoot problems and optimize process parameters. Engineers often need to adapt quickly, apply problem-solving skills, and implement robust validation protocols to ensure successful scale-up.

What is the difference between Process Development Engineer vs Manufacturing Engineer?

AspectProcess Development EngineerManufacturing Engineer
Primary FocusDesigning and optimizing manufacturing processes for new productsOverseeing and improving existing manufacturing processes
Work EnvironmentR&D labs, pilot plants, early-stage productionProduction floors, plant operations
Required CredentialsBachelor's or higher in engineering, experience in process designBachelor's or higher in engineering, experience in manufacturing
Industry UsagePharmaceuticals, electronics, chemicals, biotechAutomotive, consumer goods, electronics, industrial manufacturing

While both roles involve process optimization, Process Development Engineers focus on creating and refining new manufacturing processes, often in early development stages. Manufacturing Engineers typically work on maintaining and improving existing production processes to ensure efficiency and quality in ongoing operations.

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Process Development Engineer jobs near you
Infographic showing various Process Development Engineer job openings in Fort Collins, CO as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, and 2% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $100,580 per year, or $48.4 per hour.

Validation Engineer

Agilent

Frederick, CO • On-site

Full-time

Re-posted 7 days ago

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Job Description
Agilent's Advanced Therapeutics Division is a contract development and manufacturing organization providing products and services for our clients that provide medicines for many indications improving health for patients.
Join our team with this exciting opportunity to support commissioning Qualification and Validation (CQV) activities (excluding process validation) at our facilities in Colorado. Work in our dynamic, fast paced, API-Biopharma manufacturing environment with the ability to contribute to the growing industry of oligonucleotide (DNA-RNA) based therapeutics.
This position will be focused on the field of cleaning validation, specifically supporting laboratory studies including method verification, cleanability studies, and surface recovery to aid in MACO and ARL calculations. Additional responsibilities include support of all other areas of the engineering validation program as indicate below.
Responsibilities and essential functions may include but are not limited to:
  • Generate and review validation study documentation including validation plans, change controls, protocols, requirements specifications, asset induction requests, commissioning documentation, final reports and addenda while ensuring compliance with cGMP requirements.
  • Execute validation studies in support of engineering, manufacturing, process development, facilities, IT, quality control, and quality assurance.
  • Manage or support the validation program. Suggests, develops and/or implements improvements to the program to ensure it maintains compliance with current regulatory and industry expectations.
  • Support validation deliverables related to Equipment, Instruments, Facilities, Utilities, Cleaning, Computerized Systems and ongoing validations, as needed.
  • Generate, revise and execute validation documentation for analytical instruments, process equipment and facility computer systems and software ensuring compliance with 21 CFR, ICH, Eudralex Volume 4 Annex 15, GAMP and other regulatory and industry standard requirements as deemed necessary.
  • Support Engineering (ENG), Facilities (FAC), Manufacturing (MFG), Process Development (PD), Quality Control (QC), Quality Assurance (QA) and Information Technology (IT) with validation activities. This includes management and support of validation planning and scheduling for overall project timelines and site objectives.
  • Generate and revise documentation including, but not limited to, plans, risk assessments, traceability matrices, policies, procedures, equipment characterization reports, summary reports, specification documents and vendor qualification documents for validation studies ensuring compliance with QA and cGMP systems.
  • Responsible for generating, executing, reviewing and approving validation protocols for equipment, instruments, utilities, and control systems through commissioning, URS, Software Acceptance Testing (SAT), IQ, OQ, PQ and cleaning phases.
  • Responsible ongoing validation efforts of systems including Controlled Temperature Units (CTUs), Autoclaves, Lyophilizers, QC Glasswashers, Periodic Review
  • Generate data and reports for the periodic review and/or periodic monitoring programs.
  • Participate in both factory and site acceptance testing for new manufacturing and engineering equipment.
  • Support facility qualification of classified environments.
  • Assist with spreadsheets validation activities.
  • Support the generation and execution of cleaning validation support activities, such as: sprayball coverage testing, cycle development studies, equipment characterization reports, and equipment sampling SOPs.
  • Manage, schedule, and/or support laboratory-based cleaning validation studies, including but not limited to method validations and surface recovery studies (i.e. worst-case soil studies).
  • Support Manufacturing, Engineering, Quality Assurance (QA), and Quality Control (QC) to evaluate and resolve equipment cleaning issues and failures and to address any cleaning or cleaning validation related activities.
  • Resolve CAPA's, nonconformances, protocol incidents, and change controls related to validation.
  • May serve as a validation subject matter expert for client and regulatory audits.
  • May be responsible for attending client meetings as an engineering representative for purposes of addressing validation topics.
  • Knowledge of pharmaceutical manufacturing processes, quality improvements, and efficiency as well as knowledge of governing FDA (e.g. 21 CFR 11, 210, 211 and ICH Q7) and international regulations pertaining to the production of APIs and drug products.
  • Experienced in working with validation programs, Nonconformance Investigations, Corrective Action/Preventive Action (CAPA) and Change Control.
  • Skill in managing various projects; must be able to use individual discretion in completing work assignments; ability to work effectively as a team while making independent decisions on various tasks.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Qualifications
  • Bachelor's Degree (B.S.) or equivalent in engineering or life sciences fie
  • 1+ years relevant experience.
  • Should possess a strong quality orientation, excellent communication skills, ability to work in a fast-paced team environment, high attention to detail and high ethical standards.

Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least August 3, 2026 or until the job is no longer posted.
The full-time equivalent pay range for this position is $82,480.00 - $128,875.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations
Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.
Travel Required:
Occasional
Shift:
Day
Duration:
No End Date
Job Function:
Manufacturing

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