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Senior Process Engineer

New Generation Wellness Inc · Colorado Springs, CO

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Level
Senior
Team
Process
Base pay
$110k–$130k
Degree
Required
Certification
Black Belt preferred
Industry
Industrial
Posted
Recently

The role in 30 seconds

A senior process role at New Generation Wellness Inc (industrial) in Colorado Springs, CO.

They ask for
degree required · Black Belt preferred
Tools it names
Lean, Six Sigma, Green Belt, Kaizen, Value stream mapping, OEE
Base pay
$110k–$130k

Read from the posting. The full description is below.

From the plant jobs report · week of October 19, 2026

Process Engineer roles in Colorado: typical posted base $100k–$130k. This one lists $110k–$130k.

Median of the low and high ends of 8 live postings that list pay, out of 19 process engineer openings in Colorado, read from manufacturers' own careers sites.

Colorado plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 18 other live process postings in Colorado.

Base pay
About 10% above similar roles

Typical $95k–$123k, from 7 postings that list pay.

Experience asked
Not stated

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • ✓ Root cause 47%
  • ✓ Validation (IQ/OQ/PQ) 47%
  • ✓ Lean 42%
  • ✓ New product launch 37%
  • Tooling 32%
  • ✓ Six Sigma 26%

✓ = this posting asks for it too. % = share of similar postings that mention it.

Stands out: this posting asks for OEE, which few similar roles mention. If you have it, lead with it.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Process team at New Generation Wellness Inc

    Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Is the work mostly new product launches or sustaining existing lines?
    • How much time do you spend on the floor versus at a desk?
    • The posting mentions a Black Belt. Does the company sponsor certification?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

Full description from New Generation Wellness IncAs posted on their careers site.Show

Position Summary

The Senior Process Engineer is responsible for designing, optimizing, and scaling manufacturing processes that produce high ‐ quality nutraceutical products efficiently, safely, and in compliance with cGMP. This role leads process development and validation from pilot through commercial scale, drives continuous improvement, and partners cross ‐ functionally with Product Development, Quality, and Operations. The ideal candidate brings deep process engineering expertise in solid dose/gummy/softgel manufacturing, with a strong command of cGMP (21 CFR Part 111/117), process improvement/validation/controls, and Lean Six Sigma methodologies.

Education / Certifications

  • ✓Bachelor's degree in Chemical Engineering, Industrial Engineering, Food Engineering, Food Science, Pharmaceutical Sciences, or a closely related field.
  • ✓Lean Manufacturing certification or Six Sigma Green Belt or equivalent.

Required Knowledge

  • ✓Functional knowledge of current industrial practices related to wet and dry granulation, 2-piece encapsulation, tablet compression, softgel encapsulation, and gummy manufacturing.
  • ✓Deep, demonstrable knowledge of 21 CFR P
Show full description ↓

Senior Process Engineer

Hot Job

Colorado - Colorado Springs, CO 80905

Overview

Description

About NGW

As we prepare to embark on our centennial journey, New Generation Wellness (NGW) is not just marking a milestone; we are celebrating a century of commitment to health, vitality, and positive transformation. For 100 years, we've been at the forefront of wellness, pioneering innovation, and shaping the future of holistic health. We invite you to be part of our legacy. Joining New Generation Wellness means becoming a part of a dynamic and successful team that values innovation, collaboration, and exceeding the needs of our customers. Here's to the next 100 years of New Generation Wellness! More importantly, here's to your success!

Employee Policy

All New Generation Wellness employees are expected to exhibit professional conduct, maintain confidentiality, and display a positive attitude while performing their jobs. Employees are expected to develop teamwork, assist others when necessary, and participate willingly in any and all duties required of them for the welfare of the company. All employees are expected to learn about our company, goals, core values, mission statement, and applicable policies.

Process Development & Optimization

  • •Lead process development activities for new and existing supplement products across dosage forms including capsules, tablets, powders, softgels, and gummies.
  • •Design and execute process scale-up from pilot/bench scale to full commercial manufacturing with documented justification and data analysis.
  • •Design and execute waste stream and value stream mapping studies, process characterization, and performance vs capability analyses to enhance efficiency of manufacturing, bolster first-pass quality metric (internally denoted as 'First Time Right' metric), and increased cost savings for the organization.
  • •Establish and maintain Critical Process Parameters (CPPs), Critical Quality Attributes (CQAs), and control strategies for all manufacturing processes.
  • •Continuously analyze production data to identify improvement opportunities and drive measurable gains in yield, reduction in machine down-time, and overall equipment effectiveness (OEE).
  • •Drive post-launch process optimization for commercialized products, using production performance data, consumer feedback, and quality trends to identify and implement targeted improvements that reduce variability, improve consistency, and lower cost of goods.

Validation & Compliance

  • •Author and execute process validation protocols (IQ/OQ/PQ) in full compliance with 21 CFR Part 111 cGMP requirements.
  • •Maintain process documentation including SOPs, manufacturing batch records (MBRs), and change control records in collaboration with internal Documentation Specialist(s), Product Development, and Quality Assurance.
  • •Support internal quality audits, inspections, and UL/NSF or third-party certification reviews as requested.
  • •Lead investigation and root cause analysis for manufacturing deviations and out-of-specification (OOS) results, authoring CAPAs to allow for effective closure with assistance of Quality Assurance.

Cross-Functional Collaboration

  • •Provision of day-to-day technical assistance to Operations for product manufacturing run challenges and training of Operators where applicable.
  • •Partner with Product Development and Operations to qualify new product formulations, ensuring seamless transfer to manufacturing.
  • •Work with Product Development, Quality Control, and Quality Assurance to evaluate raw material specifications and supplier qualifications.
  • •Serve as a technical resource for Sales and Marketing during customer inquiries and product capability discussions as requested.

Continuous Improvement & Leadership

  • •Champion a culture of continuous improvement using Lean, Six Sigma, and Kaizen methodologies across the manufacturing floor.
  • •Conduct structured post-launch reviews for all new products at 30-, 90-, and 180-day intervals, benchmarking actual process performance against validation targets and initiating improvement projects where gaps are identified.
  • •Maintain a living continuous improvement roadmap for all manufacturing lines, prioritizing initiatives by impact on quality, efficiency, and cost.
  • •Lead or participate in capital improvement projects, including equipment procurement, FAT/SAT, installation, and qualification.
  • •Mentor employees (as needed) and cross-train production team members on process best practices and GMP expectations.
  • •Track and report on product development KPIs including first-pass yield, scrap rates, machine usage and deviation frequency in collaboration with Operations.

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