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.At Confluent, we are committed to our values of teamwork, innovation, accountability, integrity, leadership, and customer focus, and we invest in a team who represents these values.
Every member of our team plays a critical role in delivering life-saving medical devices through innovative materials science, engineering, and manufacturing.
We are the medical device industry's most trusted partner, and we accomplish this with an organization focused on safety, efficiency, and customer satisfaction.We are looking for a Quality Control Inspector I to join our team in Costa Rica.
If you enjoy working in a fast-paced environment and making an impact on our life-saving work, this may be a good fit for you!
As a uniquely qualified candidate, you will:SUMMARY: Works on most assignments with instructions about the general results expected.
Performs mechanical, developmental or test technician duties in such areas as: manufacturing, quality, or engineering, where some judgment, calculations and recording is required.
Inspection, adjustments, testing and equipment maintenance is required.ESSENTIAL DUTIES AND RESPONSABILITIES include the following.
Other duties may be assigned.Opens reviews and closes nonconformance's reports.Responsible for operating testing services and equipment in the production floor.Conducts receiving inspections; in process inspections and final inspections as required per inspection plans.Executes documentation review for accuracy, completeness for product release, closing of job travelers and issuance of product Certificate of ComplianceUses company records systems to perform product data searches.Enters data into data collection system (Servoy).
Execute work assignments assigned by an engineer and/or Quality control Inspection Leader or QC Supervisor.Maintains clean and orderly work area.
Self-motivated and results-oriented.Follows standard operating procedures for all tasks.Understands and complies with the quality system of the local site.Responsible for completing all appropriate quality safety and environmental hazard training and complying with applicable safety requirements.EDUCATION and/or EXPERIENCE:High school degree and technical studies in QualityWith 3-4 years of experience in quality or medical devices industry.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.
