Job Title: Process Engineer / Manufacturing Engineer Insert Molding
Location: Maumelle, AR
Experience Required: Minimum 5 years

Job Description:
We are seeking an experienced Process Engineer / Manufacturing Engineer with a strong background in insert molding to join our team in Maumelle, AR. The ideal candidate will have a minimum of 5 years of hands-on experience in managing and optimizing insert molding processes, specifically within the medical device industry. The candidate must be capable of independently handling projects related to insert molding and demonstrate expertise in delivering solutions for complex molding challenges.

Key Responsibilities:

• Lead the design, development, and optimization of insert molding processes for medical devices.
• Oversee daily manufacturing operations, ensuring efficient production, and meeting quality standards.
• Analyze current manufacturing processes and identify opportunities for cost reduction, cycle time reduction, and overall process efficiency.
• Provide technical support in troubleshooting process-related issues, resolving defects, and implementing corrective actions.
• Work closely with the quality team to ensure compliance with industry standards and regulatory requirements (FDA, ISO, etc.).
• Manage projects from concept through production, including developing project timelines, coordinating resources, and ensuring on-time delivery.
• Collaborate with product development, R&D, and other engineering teams to develop and implement new manufacturing techniques and technologies.
• Maintain comprehensive documentation of all processes, including SOPs, validation protocols, and work instructions.

Qualifications:

• Bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related field.
• At least 5 years of experience in insert molding, with a strong preference for candidates with experience in the medical device industry.
• Proficiency in process development, molding techniques, and troubleshooting insert molding processes.
• Familiarity with medical device regulatory standards such as FDA and ISO 13485.
• Ability to manage projects independently and lead process improvements.
• Strong analytical and problem-solving skills with a focus on continuous improvement.