Production Engineer - 2nd Shift

QualStaff Resources; Irvine (CA); On-site; USD 85,000 - 115,000; Full time

Job summary

QualStaff Resources in Irvine, CA is seeking a Production Engineer for the medical device manufacturing industry. The role focuses on supporting and improving manufacturing processes to boost efficiency, safety, and quality, with shifts including 2nd shift or weekend coverage.

A bachelor's degree in engineering and 2–5 years of production engineering experience in regulated environments are required, along with knowledge of GMP, ISO, and FDA regulations.

Qualifications

• Bachelor's degree in Mechanical, Manufacturing, Industrial, or Biomedical Engineering
• 2–5 years of Production Engineering experience in a medical device or regulated environment
• Knowledge of GMP, ISO, and FDA regulations
• Proficiency with manufacturing processes and process improvements
• Strong communication and problem-solving skills

Responsibilities

• Support and improve manufacturing processes for efficiency, safety, and quality
• Troubleshoot equipment and process issues using root cause analysis
• Implement continuous improvement initiatives using Lean principles
• Collaborate with cross-functional teams to meet production goals
• Ensure compliance with regulatory standards and safety protocols

Skills

Strong communication

Problem-solving

Education

Bachelor's degree in Mechanical/Manufacturing/Industrial/Biomedical Engineering

Job description

Production Engineer – Medical Device Manufacturing Industry
QUICK FACTS

• Location: Irvine, CA 92618
• Pay range: $85K – 115K
• Shifts: 2nd Shift - 3:30 p.m. to 2:00 a.m., Monday-Thursday, OR Weekend Shift - Friday through Sunday, primarily 8:00 a.m. to 8:00 p.m.
• Permanent / Direct Hire

Production Engineer – Medical Device Manufacturing Industry
QUICK FACTS

• Location: Irvine, CA 92618
• Pay range: $85K – 115K
• Shifts: 2nd Shift - 3:30 p.m. to 2:00 a.m., Monday-Thursday, OR Weekend Shift - Friday through Sunday, primarily 8:00 a.m. to 8:00 p.m.
• Permanent / Direct Hire

EXPERIENCE/EDUCATION YOU WILL NEED

• Bachelor's degree in Mechanical, Manufacturing, Industrial, or Biomedical Engineering
• 2-5 years of Production Engineering experience in a medical device or other regulated manufacturing environment
• Knowledge of GMP, ISO, and FDA regulations
• Proficiency with manufacturing processes and process improvements
• Strong communication and problem-solving skills

MAIN DUTIES OF THE JOB

• Support and improve manufacturing processes for efficiency, safety, and quality
• Troubleshoot equipment and process issues using root cause analysis
• Implement continuous improvement initiatives using Lean principles
• Collaborate with cross-functional teams to meet production goals
• Ensure compliance with regulatory standards and safety protocols

The company is an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws.