Job Title: Process/Manufacturing Engineer Insert Molding
Location: Maumelle, AR

Job Description:
We are looking for a highly skilled Process/Manufacturing Engineer with a strong background in insert molding to join our team in Maumelle, AR. The ideal candidate will have extensive experience in managing and optimizing insert molding processes, specifically within the medical device industry. The candidate will be responsible for overseeing daily operations, ensuring compliance with quality standards, and leading continuous improvement initiatives in production. This position requires a hands-on approach to troubleshooting, process enhancements, and collaboration with cross-functional teams to implement new technologies and manufacturing techniques.

Key Responsibilities:

• Lead the design, development, and optimization of insert molding processes for medical devices.
• Manage daily manufacturing operations, ensuring efficient production while maintaining quality standards.
• Analyze existing processes to identify opportunities for cost reduction, cycle time improvement, and overall process efficiency.
• Troubleshoot process-related issues, implement corrective actions, and resolve defects.
• Collaborate with the quality team to ensure processes adhere to industry standards and regulatory requirements (FDA, ISO 13485).
• Oversee project management, from concept through production, including developing timelines, coordinating resources, and ensuring on-time delivery.
• Work with product development, R&D, and other engineering teams to innovate and implement new manufacturing techniques.
• Maintain detailed documentation, including Standard Operating Procedures (SOPs), validation protocols, and work instructions for all processes.

Key Skills Needed:

• Strong background in insert molding and related manufacturing processes.
• Proficiency in process development, optimization, and troubleshooting of injection molding techniques.
• Familiarity with medical device industry standards and regulatory requirements, such as FDA and ISO 13485.
• Hands-on experience in process validation, defect resolution, and implementing continuous improvement initiatives.
• Strong project management skills, with the ability to independently manage projects and lead cross-functional teams.
• Analytical and problem-solving skills focused on cost reduction and cycle time improvements.
• Experience with SOP creation and ensuring regulatory compliance in manufacturing processes.

Qualifications:

• Bachelor's degree in Mechanical Engineering, Industrial Engineering, or related fields.
• At least 5 years of hands-on experience with insert molding, preferably in the medical device industry.
• Demonstrated expertise in handling complex molding challenges and delivering high-quality solutions.
• Excellent communication and teamwork skills to work effectively with cross-functional teams.