Operations Associate I

Confluent Medical; Warwick (RI); On-site; USD 22,000 - 35,000; Full time

Job summary

Confluent Medical Technologies in Warwick, RI invites applications for an Operations Associate I. This role supports production planning, inventory control and continuous improvement to maximize efficiency and meet service levels.

You will follow GMP and work instructions, operate light manufacturing equipment, perform assembly, inspection and measurement tasks, and document results while coordinating with the Team Lead and QA to resolve issues.

Qualifications

• Understanding of GMP and clean room requirements.
• Ability to read and follow work instructions.
• Experience with light manufacturing equipment preferred.
• Attention to detail in documentation and measurements.

Responsibilities

• Follow GMP and work instructions in assigned tasks.
• Operate light manufacturing equipment according to procedures.
• Perform assembly, inspection, and measuring of manufactured products.
• Complete documents neatly and on time.
• Collaborate with Team Lead and QA to resolve issues.

Skills

GMP understanding

Clean room following

Documentation accuracy

Attention to detail

Tools

Light manufacturing equipment

Job description

Operations Associate I### Operations Associate IApply: Warwick: Full time: Posted Yesterday: R-111686**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.