Process Engineer

The Process Engineer provides engineering support for manufacturing equipment and processes used to produce plastic medical components. This role focuses on validating processes, equipment, and tooling, driving continuous improvement, reducing scrap, and optimizing capacity to support high-quality production in a regulated medical device environment.

• Support and lead project teams to increase productivity, reduce scrap, implement lean manufacturing practices, improve system availability, enhance safety, and elevate product quality, while prioritizing projects based on potential impact and risk.
• Develop molding and extrusion processes using scientific molding best practices and industry-established methods to ensure robust, repeatable, and efficient production.
• Write, review, and execute PVP, IQ, OQ, and PQ protocols and summary reports in alignment with cGMPs, ISO standards, and other applicable medical device regulations and specifications.
• Perform root cause investigations related to NCR and CAPA processes, report findings to cross-functional teams, propose corrective actions, implement approved solutions, and verify the effectiveness of those actions.
• Develop and maintain accurate and current standard operating procedures (SOPs) for equipment operation, part inspection, equipment changeover, and preventive maintenance activities.
• Prepare capital appropriation requests for new equipment to support manufacturing, including investment justification, vendor engagement for quotes, and identification of system specifications.
• Coordinate project timelines for new equipment and process changes to meet manufacturing needs and overall project requirements.
• Support manufacturing operations by diagnosing system or process failures and collaborating with Maintenance and Tool Room personnel to implement effective system fixes.
• Coordinate engineering expertise to identify and implement safety improvements that align with OSHA standards and promote a safe working environment.
• Collaborate closely with manufacturing teams to study, evaluate, and improve equipment and processes using data-driven analysis, design of experiments (DOE), and other applicable analytical methods.

• 3–5 years of relevant process engineering or closely related experience.
• Bachelor’s degree in plastic process engineering or a related engineering field.
• Education, training, and hands-on experience with plastics and plastic processing.
• Experience with equipment and processes used to manufacture, assemble, test, and package plastic components.
• Experience using industry-standard methods for developing injection molding processes.
• Experience using industry-standard methods for developing corrugate extrusion processes.
• Ability to speak, read, write, and understand English.
• Familiarity with cGMPs, ISO standards, and medical device industry regulations and specifications.
• Ability to write, review, and execute validation documentation including PVP, IQ, OQ, and PQ.
• Demonstrated capability to perform root cause analysis and support NCR and CAPA processes.
• Strong skills in process improvement and continuous improvement within manufacturing environments.
• Experience with plastic injection molding and related process engineering.
• Ability to support and lead cross-functional project teams and collaborate effectively with manufacturing, maintenance, and tooling personnel.

• Experience working in the medical device field is preferred.
• Spanish bilingual skills are preferred.
• Background in process engineering for plastics, including plastic injection molding and plastic extrusion.
• Experience with lean manufacturing principles and methodologies.
• Ability to develop clear and accurate SOPs for equipment operation and maintenance.
• Experience preparing capital appropriation requests and justifications for new manufacturing equipment.
• Comfort working in a highly regulated environment with strict quality and safety standards.
• Interest in advanced manufacturing, automation, and capital equipment projects.
• Motivation to solve complex engineering challenges and contribute to products that improve patient outcomes.

This role is based in a manufacturing facility that produces plastic components for medical devices within a highly regulated medical device environment. Employees may be exposed to noise, chemicals, fumes, airborne particles, machinery, vibration, and other workplace hazards that are controlled in compliance with current safety and health standards. The facility emphasizes advanced manufacturing, automation, and capital equipment projects, offering cross-functional collaboration and visibility to leadership. The site serves as a center of excellence where engineers can drive meaningful improvements and see projects progress from concept to full production, contributing directly to life-saving medical devices and single-use endoscopy solutions.

This is a Contract to Hire position based out of Noblesville, IN.

The pay range for this position is $48.08 - $52.88/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)

This is a fully onsite position in Noblesville,IN.

This position is anticipated to close on Oct 3, 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 withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

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

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

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall 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 applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.