Transfer Engineer II - P22-008

at  Confluent Medical Technologies

Job Description:
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.
We are looking for a Transfer Engineer II to join our team. As a uniquely qualified candidate, you will be responsible for production planning and inventory control for multiple products while prioritizing operations to ensure maximum performance and minimum delay. This individual will take a lead role in continuous improvement, product flow and capacity improvement to improve the overall efficiency of manufacturing while service level targets.
SUMMARY: Participate on transfer teams by providing support on the systems readiness for production start up, it includes but not limited to manufacturing documentation preparation in accordance with best manufacturing practices and internal procedures and ERP system set up.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

• Contribute on maintaining safe and clean work environment by following company regulations, policies and procedures for Health, Safety and Environment.Coordinate and/or execute engineering change orders (ECO’s) to keep the documentation system in compliance with our regulation and policies as well as assure documentation is clear, updated and accurate for operators.
• Create and/or update the production control system (Epicor) with proper method of manufacturing, standard times and yield.
• During the manufacturing transfer process, manage operators’ daily activities to ensure training is completed as scheduled.
• Setup and validate production lines for manufacturing in the receiving site.Write internal technical reports.Properly document activities in accordance with the best engineering practices, company procedures, and regulatory requirements.
• Practice company safety, quality policies and procedures, actively requires conformance.
• Conducts experiments, records test procedures, collects data, and documents results in a lab notebook or appropriate document level.Sets up, adjust, and operate basic R&D laboratory/manufacturing equipment.

EDUCATION and/or EXPERIENCE:

• Bachelor’s degree in Mechanical, Chemical or Industrial Engineering, plus 2-3 years of related experience.
• Basic understanding and/or experience of Medical Device manufacture (GMP’s & GDP’s).
• Advanced english level.

COMMENTS: This position description is an outline of the major recurring responsibilities of the job. It is not intended to be all-inclusive of the work to be performed. The incumbent(s) will typically perform other related job objectives, special assignments and less significant responsibilities

• Contribute on maintaining safe and clean work environment by following company regulations, policies and procedures for Health, Safety and Environment.Coordinate and/or execute engineering change orders (ECO’s) to keep the documentation system in compliance with our regulation and policies as well as assure documentation is clear, updated and accurate for operators.
• Create and/or update the production control system (Epicor) with proper method of manufacturing, standard times and yield.
• During the manufacturing transfer process, manage operators’ daily activities to ensure training is completed as scheduled.
• Setup and validate production lines for manufacturing in the receiving site.Write internal technical reports.Properly document activities in accordance with the best engineering practices, company procedures, and regulatory requirements.
• Practice company safety, quality policies and procedures, actively requires conformance.
• Conducts experiments, records test procedures, collects data, and documents results in a lab notebook or appropriate document level.Sets up, adjust, and operate basic R&D laboratory/manufacturing equipment