FM Manufacturing Engineer II

Freudenberg Group • Jeffersonville, IN

2d

About The Position

The Manufacturing Engineer II will guide the development and optimization of manufacturing processes, including tooling design and process characterization in compliance with ISO standards, country-specific and GMP regulations. This role involves developing and maintaining detailed manufacturing documentation, specifying and coordinating the procurement, installation, and qualification of manufacturing equipment, and participating in daily production meetings. The engineer will collaborate with operations and customer service to meet project timelines, production goals, and cost targets, and proactively communicate with customers and suppliers on project matters. Additionally, the role includes training and supporting technicians and operators, analyzing and solving manufacturing issues using a structured, root-cause problem-solving approach, and leading Lean/Six Sigma projects to improve productivity, quality, delivery, and cost.

Requirements

• Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field.
• 3+ years' experience in a regulated industry.
• Proficiency in manufacturing processes used in medical device production, such as running equipment, injection molding, extrusion, catheter manufacturing, and assembly, including the materials used.
• Demonstrated experience with formal problem-solving methodologies, critical thinking, and deductive skills.
• Thorough understanding of ISO standards, particularly ISO 13485, ISO 14001, ISO 14971.
• Proficiency in GMP principles and their application in medical device manufacturing, including country-specific regulatory requirements (i.e., 21 CFR 820 in the United States).
• Understanding of process validation principles and process window/repeatability studies, DOE’s, IQ/OQ/PQ, and how to validate manufacturing processes to ensure consistent product quality and necessary safety protocols.
• Familiarity with product testing and inspection methods to ensure compliance with specifications and standards.
• Ability to maintain technical documentation, including work instructions, standard operating procedures (SOPs), and production records.

Responsibilities

• Guide the development and optimization of manufacturing processes, including tooling design and process characterization in compliance with ISO standards, country-specific and GMP regulations.
• Develop and maintain detailed manufacturing documentation, including BOMs, process flowcharts, work instructions, and test/inspection plans in compliance with quality system requirements.
• Specify and coordinate the procurement, installation, and qualification (IQ/OQ/PQ) of manufacturing equipment, fixtures, and gauges to support efficient and reliable production.
• Participate in daily production meetings (i.e., LPMS) and collaborate with operations and customer service to ensure project timelines, production goals, and cost targets are met.
• Proactively communicate with customers and suppliers on project matters, mold and fixture design/repair, validation, and product quality issues.
• Train and support technicians and operators through ongoing sustaining engineering activities.
• Analyze and solve manufacturing issues using a structured, root-cause problem-solving approach and lead cross-functional teams to implement robust, permanent solutions.
• Lead Lean/Six Sigma projects to improve productivity, quality, delivery, and cost; oversee Kaizen initiatives and eliminate waste in manufacturing processes.
• May help train new team members.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level