Manufacturing Engineer

Actalent • Glendora, CA • 4h ago

Description

This role supports and improves manufacturing operations for regulated medical device products, with a focus on process efficiency, product quality, and compliance. The engineer will work cross-functionally with production, quality, and R&D to troubleshoot issues, implement improvements, and support new product introduction.

Must-Have Qualifications

Bachelor's degree in Engineering or related technical field

5+ years of experience in a regulated manufacturing environment (medical device highly preferred)

Working knowledge of:

FDA QSR

ISO 13485:2016

EU MDR (2017/745)

Hands-on experience with process validation (IQ, OQ, PQ)

Experience with non-conformance investigations, CAPA, and root cause analysis

Strong understanding of statistical process control (SPC) and process improvement

Proficiency with SolidWorks and Microsoft Office (Excel, Word)

Key Responsibilities

Provide engineering support to production and product development teams

Develop and improve manufacturing processes, tooling, and equipment to enhance quality and reduce costs

Troubleshoot and resolve production issues related to processes and equipment

Lead and support validation activities (IQ/OQ/PQ) for new and existing processes

Investigate non-conformances and drive corrective and preventive actions (CAPA)

Maintain and update manufacturing documentation, including specifications and DCRs

Support new product introduction (NPI) and transfer from R&D into production

Partner with Quality to improve inspection methods and ensure compliance

Create and monitor SPC/control charts to drive process consistency

Assist with preventative maintenance planning and equipment support

Train production personnel on new or updated processes

Skills

Manufacturing engineering, Gmp, solidworks, npi, Process improvement, Manufacturing process, IQ, PQ, OQ, FDA, QSR, EU MDR, iso 13485, r&d, Continuous improvement, quality management, document change orders, change orders, preventive maintenance, equipment maintenance, equipment validation, equipment reliability, medical device, opthamology

Top Skills Details

Manufacturing engineering,Gmp,solidworks,npi

Additional Skills & Qualifications

Experience in ophthalmic or optometric devices

Experience supporting batch records and production documentation

Experience in equipment maintenance or manufacturing automation

Strong analytical and problem-solving skills

Ability to operate independently and collaborate cross-functionally

Effective communication and documentation skills

Detail-oriented with strong time management and prioritization ability

Experience Level

Intermediate Level

Job Type & Location

This is a Contract to Hire position based out of Glendora, CA.

Pay and Benefits

The pay range for this position is $40.00 - $60.00/hr.

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 Glendora,CA.

Application Deadline

This position is anticipated to close on Jun 25, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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.

AECOM • Orange, CA • 1d ago

IT & Engineering

Company Description Work with Us. Change the World. At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work he...

1d ago

Go to Apply