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Process Engineer Manager Jobs in Danvers, MA (NOW HIRING)

Principal Process Engineer

Bedford, MA · On-site

$150 - $165/hr

IQ, OQ, PQ, Guage R&R, DoE, process capability ... Must have experience in design requirements and risk management (pFMEA), driving risk mitigation to ...

Principal Process Engineer

Bedford, MA · On-site

$150K - $165K/yr

IQ, OQ, PQ, Guage R&R, DoE, process capability ... Must have experience in design requirements and risk management (pFMEA), driving risk mitigation to ...

... Engineer to join the Coating and Lamination Process development team. As a member of this team ... Lead the design, management, and coordination of experiments on pilot-scale roll-to-roll coating ...

Principal Process Engineer

Bedford, MA · On-site

$150 - $165/hr

Using Engineering procedures standard for research and development, carries out assignments ... Must have experience in design requirements and risk management (pFMEA), driving risk mitigation to ...

... Engineer to join the Coating and Lamination Process development team. As a member of this team ... Lead the design, management, and coordination of experiments on pilot-scale roll-to-roll coating ...

... for Engineer, Process Engineering Fueled by innovation at the intersection of biology and ... For those who supervise or manage a staff, responsible for ensuring that subordinates follow all ...

... for Engineer, Process Engineering Fueled by innovation at the intersection of biology and ... For those who supervise or manage a staff, responsible for ensuring that subordinates follow all ...

Showing results 41-60

Process Engineer Manager information

See Danvers, MA salary details

$52.3K

$97.3K

$150.7K

How much do process engineer manager jobs pay per year?

As of Aug 12, 2026, the average yearly pay for process engineer manager in Danvers, MA is $97,301.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,800.00 and $108,900.00 per year, depending on experience, location, and employer.

What is a process engineer manager?

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?

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 Danvers, MA? The most popular types of Process Engineer jobs in Danvers, MA are:
What are popular job titles related to Process Engineer Manager jobs in Danvers, MA? For Process Engineer Manager jobs in Danvers, MA, the most frequently searched job titles are:
What cities near Danvers, MA are hiring for Process Engineer Manager jobs? Cities near Danvers, MA with the most Process Engineer Manager job openings:

Principal Process Engineer

Werfen

Bedford, MA • On-site

$150 - $165/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 26 days ago


Werfen rating

8.7

Company rating: 8.7 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Introduction

Werfen

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.

Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

Overview

Position Summary:

Using Engineering procedures standard for research and development, carries out assignments associated with research, design, development, support or manufacturing of specific parts, processes, software or components of medical diagnostic systems. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Plans and conducts work requiring the application of extensive and diversified knowledge of engineering principles in broad areas of assignments and related fields. Generally, uses advanced techniques and the modification or extension of theories, concepts and practices in the specialty and/or related disciplines. Maintains a clear overview of a major product development. Makes sound judgments when compromises, necessitated by available time and technical capacity, must be made to meet set objectives. Mentors junior staff.

The annual base salary range for this role is currently $150,000 to $165,000. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs.

This role is eligible for medical, dental, and vision insurance, 401k plan retirement benefits with an employer match, as well as paid vacation and sick leave.

Responsibilities

Key Accountabilities:

Essential Functions:

  • Acts as an Individual contributor, core team or technical lead for a specific project or product line.
  • Accountable for the completion of assigned deliverables in accordance with approved schedules.
  • Authors documentation and participates in activities in support of design control.
  • Independently plans, performs & prioritizes tasks that are complex in nature, in alignment with corporate goals.
  • Analyzes and interprets data, identifying trends and formulating the next steps, while effectively performing trade off analysis, if required by the function.
  • Leads, designs and/or develops one or more of the following: new test methods, specifications, technical apparatus, software and processes for complex components and functions.
  • Experience leading the development of test strategies, execution process validation, including but not limited to: IQ, OQ, PQ, Guage R&R, DoE, process capability.
  • Must have experience in design requirements and risk management (pFMEA), driving risk mitigation to closure in collaboration with cross-functional teams.
  • Experience working with electromechanical assemblies and instrumentation and test fixtures.
  • Evaluates complex designs or processes, with respect to acceptability, suitability and cost. Recommends preferred design options. Presents trade-off, if required by the function.
  • Identifies product defects and able to recognize outliers in results. Able to explain and document product defects and their impact.
  • Effectively communicates technical information to a multidisciplinary team in the form of documentation, presentations and technical summaries and promotes collaboration.
  • Leads without authority & provides technical guidance to engineers and technicians assigned to him/her on a given project. Provides mentoring within or outside of their department.
  • Provides technical support for or leads CAPA or complaint investigations.
  • Partner with Quality Engineering and Regulatory teams to support phase planning readiness and contribute to the Design History File (DHF)
  • Independently generates predictable schedules for activities related to the function, understanding cross-functional dependencies.
  • Responsible for estimating and planning validation activities across the development lifecycle
  • Transition validated process to operations: provide training, procedures, and on-floor support

Secondary Functions:

  • May review and provide input to deliverables from other functions.
  • Recommends and drives improvement initiatives and motivates others to implement.
  • May be assigned CAPA ownership.

Budget Managed: (if applicable)

  • N/A

Internal Networking/Key Relationships:

To be determined based on department needs, to include interactions such as:

  • Will interface on a regular basis with groups across the organization as needed

Skills & Capabilities:

The ideal candidate for this position will exhibit the following skills and capabilities:

  • Statistical Analysis (if required by the function), Root Cause Analysis, Creative Problem Solving, Critical Thinking
  • Technically adept and confident
  • Leadership: Accountability, Decision Making, Influence, Communication
  • Mentoring
Qualifications

Minimum Knowledge & Experience Required for the Position:

Education:

  • Bachelor\'s degree in Engineering, Science or a related field

Experience:

  • Twelve years of product development or relevant experience
  • Eight to ten years of product development or relevant experience for advanced degrees
  • For internal candidate promotion: Demonstrated proficiency in meeting all competencies of current level and acceptable performance history may be used in lieu of experience
  • In vitro medical device experience highly desired

Additional Skills/Knowledge:

  • Language: Proficiency in English language required
International Mobility:
  • Required: No
Travel Requirements:
  • Some domestic and international travel may be required.
Closing

If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.

Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.

We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.

www.werfen.com

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What Werfen employees say

Pay

Benefits

Hours and flexibility

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About Werfen

Sourced by ZipRecruiter

Industry

Health care and social assistance

Company size

1,001 - 5,000 Employees

Headquarters location

L'Hospitalet de Llobregat, Barcelona, ES