Process Engineer

Actalent; Portage (MI); On-site; USD 76,000 - 92,000; Full time

Benefits offered by this job

Medical

Dental & Vision

401(k)

Life Insurance

Disability insurance

HSA

Transportation benefits

Employee Assistance Program

Time Off

Job summary

Actalent is seeking a Manufacturing Engineer to integrate new products into existing assembly lines. You will develop and validate manufacturing processes, create documentation, and ensure quality and safety standards are met.

The role focuses on equipment validation, line layout optimization, and PM planning to support product transfers and efficient production at the Portage, MI site.

Qualifications

• Experience with process validation and statistical methods.
• Familiar with PFMEA, Control Plan, SOP, and PPAP practices.
• Ability to map processes and perform root cause analysis.
• Experience with GMP and safety procedures.

Responsibilities

• Develop and implement manufacturing processes on existing lines for new products.
• Lead equipment validation and process validation (IQ/OQ/PQ).
• Create work instructions, PFMEAs, control plans, and specs.
• Design ergonomic line layouts and perform job hazard assessments.
• Develop PM procedures for equipment and ensure regulatory compliance.
• Support product transfers and ensure documentation per Stryker procedures.

Skills

Process validation

IQ/OQ/PQ

PFMEA

Control plans

Documentation

Line layout design

Education

Bachelor's degree in engineering

Job description

Description

As a key member of the Product Transfer Team, the Manufacturing Engineer is responsible for the seamless integration of new products into existing assembly lines. This role focuses on developing and validating manufacturing processes, ensuring they meet quality, safety, and efficiency standards.

Key Responsibilities:

• Develop and implement manufacturing processes on existing assembly lines for new product introductions.
• Lead equipment and machine validation efforts, including process validation (IQ/OQ/PQ).
• Create comprehensive documentation including work instructions, PFMEAs, control plans, and engineering specifications.
• Design and optimize line layouts with a focus on ergonomics and job hazard assessments.
• Conduct torque studies and program torque controllers to ensure process accuracy and repeatability.
• Develop Preventive Maintenance (PM) procedures for new and existing equipment.
• Prepare and submit PPAP documentation in compliance with customer and regulatory requirements.
• Generate technical views and documentation of the assembly process and line configuration.
• Drive the creation and execution of a Plan for Every Part to ensure material readiness and flow.
• Provide engineering support for product transfers ensuring that all activities are completed and documented in accordance with the latest Stryker procedures. Determine the technical objectives of engineering assignments and makes decisions regarding the direction and the results of the assignment.
• Monitor and control progress of work ensuring sound application of engineering principles and the appropriate use of policies and procedures.
• Analyze equipment to establish operating data, conduct experimental test and result analysis. May lead or act as independent reviewer in process review meetings. Coach and mentor others on functionally related topics. Ensure quality of process and product as defined in the appropriate operation and material specifications.
• Select components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols. Participate in PFMEA, Control Plan, SOP, PPAP and other internal process qualification generation associated with product transfers.
• Ensure adherence to GMP and safety procedures.
• Review and approve of validation documentation.

Qualifications

• Bachelors degree in an engineering discipline.
• Minimum of 4 or more years experience in a FDA regulated manufacturing or project environment.
• Experience of process/ product validation. Experience with statistical methods, process mapping, root cause analysis.
• Experience in executing complex problem-solving techniques related to manufacturing technical issues.

Job Type & Location

This is a Contract position based out of Portage, MI.

Pay and Benefits

The pay range for this position is $55.00 - $67.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical
• dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Portage,MI.

Application Deadline

This position is anticipated to close on Oct 21, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.