Operations Associate I

CONFLUENT MEDICAL TECHNOLOGIES INC.; Town of Warwick (NY); On-site; USD 22,000 - 34,000; Full time

Job summary

Confluent Medical Technologies Inc. is seeking an Operations Associate I to oversee production planning and inventory control across multiple products, ensuring priority of operations for optimal efficiency and minimal delays.

The role requires adherence to GMP and 5S standards, with responsibilities spanning documentation, equipment operation, and ongoing process improvement to boost throughput and reduce downtime.

Qualifications

• GMP knowledge and clean room procedures.
• Ability to follow work instructions and SOPs.
• Experience with production planning or inventory control is a plus.

Responsibilities

• Follow GMP rules, work instructions, documentation, and clean room requirements.
• Operate light manufacturing equipment per instructions and procedures.
• Assemble, chemical scouring, visually inspect, and measure manufactured products.
• Review and complete documents neatly and accurately.
• Communicate concerns or issues arising during production to Team Lead or Supervisor.
• Maintain 5S standards and keep the work area clean and organized.
• Fulfill other duties as assigned.

Skills

GMP knowledge

Documentation

Inventory control

Job description

Salary Range: $16.00 - $25.25 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 Operations Associate I 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

The position will have responsibility for following all Work Instructions for assigned tasks in accordance with internal policies and procedures.

Essential Duties and Responsibilities Include, but not limited to, the following:

• Understand and follow all rules related to GMP, work instructions, documentation completion, and clean room requirements.
• Able to operate light manufacturing equipment according to instructions, specifications and procedures.
• Perform tasks related to assembly, chemical scouring, visual inspection, and measuring manufactured products.
• Perform all duties in a skilled and timely manner.
• Review and accurately complete all documents and required forms neatly and legibly.
• Work to detect and help overcome issues or concerns associated with products or processes if/when they arise.
• Communicate any concerns or issues which arise during the production process to the Team Lead or Supervisor.
• Maintain positive working relationships with co-workers and support groups.
• Maintain cleanliness standards required for 5S in the personal work area.
• Adhere to and support company policies and procedures.
• Will be required to perform other duties as assigned.

Supervision Received General Direction: Received from the Team Lead and/or Supervisor with respect to assignments, priorities and overall objectives; work in coordination with R&D Engineering and Quality as needed.

Other Duties and Responsibilities Include the following.

Other duties may be assigned.

• Comply with all safety policies, practices and procedures.
• Report all unsafe activities to the Team Lead, Supervisor, and/or Human Resources.
• Participate in proactive team efforts to achieve departmental and company goals.
• Perform other duties as assigned.

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 and tubing, balloon expandable stents and catheters, complex catheters, biomedical textiles, and high precision polymer tubing. 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 regret that we are unable to sponsor employment visas or consider individuals on time-limited visa status for this position.

Confluent Medical Technologies is an equal opportunity employer. Only qualified candidates will be contacted.

Applying materials science to MedTech innovation.

Confluent specializes in expert design and development of large-scale manufacturing specializing in interventional catheter-based devices and implants. Our key capabilities include Nitinol components and tubing, balloon and complex catheters, high-precision polymer tubing, and implantable textiles. We operate in 8 state-of-the-art facilities across the United States and Costa Rica and currently employ over 2,000 employees. Confluent has earned the confidence of leaders in the medical device community through a proven track record of innovation, engineering, and manufacturing. Visit www.confluentmedical.com to learn more.