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Process Engineer Process Engineer Jobs in Wilton, CT

Glanbia

Process Engineering Manager

West Haven, CT · On-site

Process Engineering Manager at Glanbia Join this dynamic team focused on delivering better nutrition for every step of life's journey ! The Opportunity The Process Engineering Manager leads complex ...

Glanbia

Process Engineering Manager

West Haven, CT · On-site

Process Engineering Manager at Glanbia Join this dynamic team focused on delivering better nutrition for every step of life's journey ! The Opportunity The Process Engineering Manager leads complex ...

Glanbia

Process Engineering Manager

West Haven, CT

Process Engineering Manager Opportunity at Glanbia Join this dynamic team focused on delivering better nutrition for every step of life's journey ! The Opportunity The Process Engineering Manager ...

Ametek

Sr Engineer, Plastics

Bridgeport, CT

$105K - $136K/yr

The Plastics/Injection Molding Engineer is responsible for driving mold process development and injection molding projects through adherence to established product design, scientific injection ...

Ametek

Sr Engineer, Plastics

Bridgeport, CT · On-site

$105K - $136K/yr

Experienced in process development utilizing Scientific Molding and Design Of Experiments (DOE ... Work with other engineers and production operators in process development. * Occasionally ...

AMETEK, Inc.

Sr Engineer, Plastics

Bridgeport, CT · On-site

$105 - $130/hr

Experienced in process development utilizing Scientific Molding and Design Of Experiments (DOE ... Work with other engineers and production operators in process development. * Occasionally ...

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All JobsProcess Engineer Process Engineer JobsProcess Engineer Process Engineer Jobs in Wilton, CT

Process Engineer Process Engineer information

See Wilton, CT salary details

$51.3K

$95.3K

$147.6K

How much do process engineer process engineer jobs pay per year?

As of Aug 19, 2026, the average yearly pay for process engineer process engineer in Wilton, CT is $95,309.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,200.00 and $106,700.00 per year, depending on experience, location, and employer.

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

AspectProcess EngineerProcess Engineer
CredentialsBachelor's in Engineering or related field, certifications like Six Sigma often preferredBachelor's degree in Chemical, Mechanical, or Industrial Engineering; certifications like Six Sigma are common
Work EnvironmentManufacturing plants, chemical facilities, or production linesIndustrial settings, plant floors, or process development departments
Industry UsageManufacturing, chemical, oil & gas, pharmaceuticalsSimilar industries, often overlapping in chemical, manufacturing, and energy sectors

Both roles focus on optimizing manufacturing processes, ensuring safety, and improving efficiency. They often share similar qualifications and work environments, making them closely related in the industry.

What job categories do people searching Process Engineer Process Engineer jobs in Wilton, CT look for?

The top searched job categories for Process Engineer Process Engineer jobs in Wilton, CT are:

What cities near Wilton, CT are hiring for Process Engineer Process Engineer jobs?

Cities near Wilton, CT with the most Process Engineer Process Engineer job openings:

Process Engineer Process Engineer jobs near you

Sr. Scientist/Engineer, Process Development

MannKind Corporation

Danbury, CT • On-site

$120 - $180/hr

Other

Re-posted 3 days ago

Job description

MannKind Corporation is a biopharmaceutical company focused on transforming chronic disease care through patient-centric solutions, developing and commercializing inhaled therapeutics and drug-device technologies for unmet needs across endocrine, cardiorenal, and orphan lung diseases.

At MannKind, our employees are a core asset, and we foster a collaborative culture where each team member contributes to improving health outcomes and changing lives.

Position Summary

Provide advanced scientific and technical leadership in the development, optimization, scale-up, and lifecycle management of pharmaceutical manufacturing processes across the product lifecycle. Operate as a senior individual contributor within the process development department, applying independence, technical judgment, and subject-matter expertise. Support clinical and commercial manufacturing by ensuring processes are scalable, robust, and compliant, while contributing to cross-functional technical decision-making and continuous improvement across MannKind’s product portfolio.

Essential duties and responsibilities
  • Lead the design, development, and optimization of pharmaceutical manufacturing processes from late-stage development through commercialization.
  • Apply sound scientific principles, experimental design, and data-driven methodologies to establish process understanding and improve process robustness and capability. Independently plan, execute, analyze, and document complex experimental studies in support of process development and process characterization.
  • Serve as a subject matter expert for specific unit operations, process technologies, or platform processes, providing technical guidance across functions.
  • Support process scale-up, technology transfer, and process validation activities by generating technical documentation and providing hands-on consultative support.
  • Collaborate cross-functionally with manufacturing, engineering, quality, analytical development, regulatory, and external partners to ensure successful process implementation.
  • Manage equipment maintenance, including calibrations/qualifications.
  • Support investigations related to process deviations, manufacturing issues, and continuous improvement initiatives.
  • Author and review development reports, protocols, technical summaries, and regulatory documentation in compliance with cGMP and regulatory expectations.
  • Contribute to process lifecycle management activities, including continuous improvement, change management, and technical risk assessments.
  • Provide technical mentorship and informal coaching to junior scientists and associates to elevate team technical capability.
  • Observe all Company, Health, Safety and Environmental guidelines.
  • Duties and responsibilities are not limited to the work listed above and may include other assignments as necessary.
Minimum qualifications
  • BS/BA with 6-8 years, MS with 4–6 years or PhD, or relevant experience in Chemistry, Chemical Engineering or a related field, with experience in pharmaceutical process development and/or manufacturing support.
  • Experience in the development and scale-up of drug manufacturing processes.
  • Experience preferred in the manufacture, packaging, and kitting of clinical phase drug products.
  • Experience with orally inhaled dosage forms is strongly preferred.
  • Experience with the following unit operations preferred: spray drying, wet nano-milling, tangential flow filtration, micro fluidization.
  • Experience managing second-party resources, including clinical packaging vendors and contract development and manufacturing organizations.
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