1

Process Engineer Manager Jobs in Rhode Island (NOW HIRING)

The Process Engineer is a key member of the operations and engineering team, responsible for ... Lead Management of Change (MOC) activities * Participate in product/process transfers through a ...

The Process Engineer is a key member of the operations and engineering team, responsible for ... Lead Management of Change (MOC) activities * Participate in product/process transfers through a ...

The Process Engineer is a key member of the operations and engineering team, responsible for ... Lead Management of Change (MOC) activities * Participate in product/process transfers through a ...

The position requires interpreting SPC (Statistical Process Control) data, managing material ... The Senior Engineer will play a key role in ensuring the smooth operation and ongoing success of ...

The position requires interpreting SPC (Statistical Process Control) data, managing material ... The Senior Engineer will play a key role in ensuring the smooth operation and ongoing success of ...

The position requires interpreting SPC (Statistical Process Control) data, managing material ... The Senior Engineer will play a key role in ensuring the smooth operation and ongoing success of ...

The engineer is responsible for initiating and managing trial casting work orders, evaluating ... Capture and analyze process data to diagnose deviations and recommend iterative adjustments to ...

next page

Showing results 1-20

Process Engineer Manager information

See Rhode Island salary details

$48.5K

$90.1K

$139.6K

How much do process engineer manager jobs pay per year?

As of Jun 18, 2026, the average yearly pay for process engineer manager in Rhode Island is $90,114.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,000.00 and $100,900.00 per year, depending on experience, location, and employer.

What are Process Engineer Managers?

Process Engineer Managers are professionals responsible for overseeing and improving manufacturing or production processes within an organization. They lead teams of process engineers, coordinate projects aimed at optimizing efficiency, quality, and safety, and ensure compliance with industry standards. Their role often involves analyzing workflows, implementing new technologies, and collaborating with other departments to achieve organizational goals. Additionally, they may manage budgets, provide technical support, and mentor junior engineers.

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

AspectProcess EngineerProcess Engineer Manager
ResponsibilitiesDesign, optimize, and implement manufacturing processesOversee process engineering teams, develop strategies, and ensure project delivery
Required SkillsProcess design, problem-solving, technical knowledgeLeadership, project management, technical expertise
CertificationsPE license often preferred, Six Sigma, Lean certificationsSame as Process Engineer, plus management training
Work EnvironmentManufacturing plants, engineering officesManufacturing plants, engineering departments, management offices

The main difference is that Process Engineer Managers lead teams and develop strategies, while Process Engineers focus on designing and optimizing processes. Both roles require similar technical skills and certifications, but the manager role adds leadership and project oversight responsibilities.

How does a Process Engineer Manager typically collaborate with cross-functional teams to implement process improvements?

A Process Engineer Manager often works closely with teams from production, quality assurance, maintenance, and supply chain to identify inefficiencies and develop solutions. This collaboration involves leading meetings to gather input, aligning on project goals, and ensuring all stakeholders are informed throughout the implementation process. The manager also facilitates training sessions for staff on new procedures and monitors the impact of changes, making adjustments as needed. Effective communication and leadership are essential to foster teamwork and drive successful process improvements.

What are the key skills and qualifications needed to thrive as a Process Engineer Manager, and why are they important?

To thrive as a Process Engineer Manager, you need a strong background in process engineering, project management, and a relevant engineering degree, often supported by experience in manufacturing or industrial settings. Familiarity with Lean Six Sigma methodologies, process simulation software, and ERP systems is typically required, and certifications like PMP or Six Sigma Black Belt are advantageous. Excellent leadership, problem-solving, and communication skills help you effectively manage teams and drive process improvements. These skills ensure efficient operations, cost savings, and the successful implementation of process enhancements across the organization.
What are the most commonly searched types of Process Engineer jobs in Rhode Island? The most popular types of Process Engineer jobs in Rhode Island are:
What cities in Rhode Island are hiring for Process Engineer Manager jobs? Cities in Rhode Island with the most Process Engineer Manager job openings:
Infographic showing various Process Engineer Manager job openings in Rhode Island as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,114 per year, or $43.3 per hour.
Process Engineer

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago


Job description

Title: Process Engineer

Location: Providence, RI

Our client, a leading global company specializing in custom solutions for the medical device and pharmaceutical industries, is seeking a Process Engineer for its Providence, RI location. The company designs and manufactures custom components using advanced plastic manufacturing technology and rigorous quality control standards.

Position Overview

The Process Engineer works closely with Operations, Quality, and Design teams to establish and sustain process capability across the company's Americas operations. This role applies engineering principles, statistical methods, and process development expertise to optimize product quality, ensure regulatory compliance, and drive continuous improvement from development through full-scale production.

Responsibilities and Functions:

  • Develop and execute IQ/OQ/PQ validation protocols for thermoforming and sealing processes in compliance with ISO 11607-2 and FDA process validation guidance.
  • Define critical process parameters (CPPs), Proven Acceptable Ranges (PAR), and Normal Operating Ranges (NOR) through structured development studies and DOE.
  • Lead statistical analysis of validation data including process capability (Cpk), targeting a minimum Cpk of 1.33 for critical parameters.
  • Own the full three-stage validation lifecycle: Process Design, Process Qualification, and Continued Process Verification.
  • Define, optimize, and standardize process parameters including temperature profiles, vacuum/pressure settings, plug assist timing, and cycle times.
  • Lead equipment qualification (IQ/OQ) for supporting equipment.
  • Ensure all processes comply with ISO 13485, ISO 11607-1/2, and FDA 21 CFR Part 820 (QMSR); serve as subject matter expert during internal, customer, and regulatory audits.
  • Use Minitab or equivalent software for DOE, capability studies, SPC, Gage R&R, and process data analysis.
  • Lead PFMEA, CAPA, and root cause investigations using structured methodologies (5-Why, Fishbone, DMAIC).
  • Partner cross-functionally with Operations, Quality, Supply Chain, and Design to align process improvements with business and customer requirements.
  • Train production teams on validated processes, in-process monitoring requirements, and critical quality attributes.
  • Apply Lean Manufacturing and Six Sigma principles to eliminate waste and improve process efficiency.

Qualifications:

Education:

  • Bachelor's degree in Mechanical, Manufacturing, Industrial, Chemical Engineering, or a related field. Advanced degrees or certifications (Six Sigma, CQE, CQA) are a plus.

Experience:

  • 3–5+ years in process engineering, manufacturing engineering, or operations engineering within a regulated industry; medical device experience strongly preferred.
  • Hands-on experience with process validation (IQ/OQ/PQ).
  • Strong working knowledge of ISO 13485 and FDA 21 CFR Part 820 — must be able to serve as subject matter expert during audits.
  • Demonstrated expertise in DOE and Six Sigma methodology; Black Belt certification preferred.
  • Proficiency with Minitab or equivalent statistical software for capability analysis, SPC, and DOE.
  • Experience with CAPA and structured problem-solving methodologies.
  • Familiarity with plastic manufacturing processes, polymer materials, heat sealing, and packaging equipment.
  • Strong leadership skills with the ability to influence across Operations, Quality, and Design.

Benefits:

  • 401(k) match program
  • Dental, health, and vision insurance
  • Paid time off

Location: Providence, RI — occasional travel to other sites may be required.

If you are interested in this position, please apply here or send your resume to matthew@mrrecruiter.com.

Equal Opportunity Employer Disclaimer

This organization is an Equal Opportunity Employer and is committed to creating an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability status, genetic information, protected veteran status, or any other characteristic protected by applicable law. Employment decisions are based solely on qualifications, merit, and business needs.