Operations Associate I

Posted 2 Days Ago
Be an Early Applicant
Alajuela, Alajuela
Entry level
Healthtech
The Role
The Operations Associate I will perform and document production functions for the fabrication, modification, and assembly of medical devices. Responsibilities include operating manufacturing equipment, conducting process tests for quality compliance, maintaining a clean work area, and ensuring safety regulations are followed.
Summary Generated by Built In

We are looking for a 

Operations Associate I

to join our talented team in

Costa Rica

.
As a uniquely qualified candidate, you will:

Job Description:

Supervisor: Greivin Jiménez

Horario: Turno A

Edificio: B25

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 an Operations Associate 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: Under direct supervision, performs and documents production functions relating to fabrication, modification and assembly of components or finish medical devices.

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

  • Performs and documents operations in the production process.
  • Sets up, adjust and operates laboratory/manufacturing equipment.
  • Performs process/product tests and audits for conformity to quality and/or regulatory requirements.
  • Performs self-inspections of own work.
  • Follows standard operating procedures for all tasks.
  • Maintains clean and orderly work area.
  • Has completed all appropriate safety and environmental hazard training.
  • Responsible for ensuring personal and company compliance with local and company regulations, policies and procedures for Health, Safety and Environmental compliance.

EDUCATION and/or EXPERIENCE: Elementary school, 0-1 year of related experience and/or training; or equivalent combination of education and experience. Basic personal computer skills.

OTHER SKILLS and ABILITIES:   Ability to read and understand technical documentation associated with specific discipline. Must be able to successfully complete company/department training courses in manufacturing techniques. Ability to learn regulatory (GMP) requirements.

Ability to read and comprehend simple instructions.

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.

Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.

COMMENTS:  This job 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. Other related job objectives, special assignments and less significant responsibilities will typically be performed by the incumbent(s).

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.

The Company
HQ: Scottsdale, AZ
1,068 Employees
On-site Workplace
Year Founded: 1991

What We Do

Confluent Medical Technologies applies 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.

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