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, pr…
Skills: Supplier Auditing, Quality Systems, CAPA, SCAR, ISO Standards
Abbott
Team Member I (Referred B31)
Alajuela, Alajuela Province, Costa Rica · On-site
Entry level$20B raised
JOB DESCRIPTION: Job Description Operario(a) de Producción Abbott B31 Turno A: lunes a viernes de 5:50am a 3:15pm. Turno B: lunes a viernes de 3:15pm a 10:00pm y sábados de 7:00am a 2:30pm. Turno C: sábado a domingo de 1…
Skills: Medical Device Production, GMP, GDP, Product Inspection, Line Cleaning
Job Description: Confluent Medical Technologies es una empresa de dispositivos médicos financieramente sólida y en rápido crecimiento, dedicada a trabajar en colaboración con nuestros clientes, llevando sus proyectos des…
Skills: Inventory Control, Material Handling, Production Planning, Warehouse Operations, Picking and Packing
Job Description: Confluent Medical Technologies es una empresa de dispositivos médicos financieramente sólida y en rápido crecimiento, dedicada a trabajar en colaboración con nuestros clientes, llevando sus proyectos des…
Skills: Production Management, Quality Control, Team Leadership, Medical Device Manufacturing, Regulatory Compliance
Regente Farmacéutico 3 días - Zona Alajuela (La Guácima)
Alajuela, Alajuela Province, Costa Rica · On-site
Mid level
1. Propósito de la posición Garantizar la operatividad de las farmacias desde el ámbito técnico, en cumplimiento de las normas de habilitación de farmacias dictadas por las instituciones gubernamentales de control, así …
Job Description: Confluent Medical Technologies es una empresa de dispositivos médicos financieramente sólida y de rápido crecimiento, dedicada a trabajar de manera colaborativa con nuestros clientes, llevando sus proyec…
Job Description: SUMMARY: Manufactures products and carries out supervisory responsibilities in accordance with the organization´s policies and applicable labor law; organizing and monitoring work flow. SCHEDULE: Diurno …
Skills: Production Management, Lean Manufacturing, Personnel Supervision, Quality Control, Labor Law Compliance
Summary of Duties and Responsibilities / Resumen de Funciones y Responsabilidades: Diseñar y desarrollar los sistemas de control automático de nuevos dispositivos y equipos automatizados para mejorar los procesos de manu…
Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. A Design Quality Engineer will be part of a cross-functional team for new product development to deliver safe and eff…
Skills: Design Controls, Risk Management, FMEA, Test Method Validation, Measurement Systems Analysis
Specialist – Statistical/Clinical Programming (Alajuela, Costa Rica)
Alajuela, Alajuela Province, Costa Rica · Hybrid
Mid level
Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Founded in 1856, Smith+Nephew is one of the longest-established medical device companies in the world, and has been t…
Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Founded in 1856, Smith+Nephew is one of the longest-established medical device companies in the world, and has been t…
Skills: Biostatistics, SAS, R, Clinical Study Design, Statistical Analysis Plans
Job Description: Confluent Medical Technologies se dedica a trabajar en colaboración con nuestros clientes, llevando sus proyectos desde el prototipo rápido hasta la producción de gran volumen. Nuestros conocimientos téc…
Equipment Technician II (Turno Nocturno 4x3 M a S)
Alajuela, Alajuela Province, Costa Rica · On-site
Mid level
Job Description: 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 t…
Job Description: 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 t…
Job Description: Confluent Medical Technologies se dedica a trabajar en colaboración con nuestros clientes, llevando sus proyectos desde el prototipo rápido hasta la producción de gran volumen. Nuestros conocimientos téc…
Skills: Medical Device Manufacturing, Quality Auditing, Technical Documentation, Standard Operating Procedures, Manual Dexterity
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, pr…
Skills: Production Planning, Inventory Control, Continuous Improvement, Root Cause Analysis, Process Validation
REQUISITOS: •Primaria Concluida. •Conocimiento básico de Office (word,excel,power point). •Capacidad de hacer cálculos matemáticos. •Conocimientos en Industria Médica (dese…
Skills: Microsoft Office, Mathematical Calculations, Hand Tool Handling, Assembly, Packing
REQUISITOS: •Primaria Concluida. •Conocimiento básico de Office (word,excel,power point). •Capacidad de hacer cálculos matemáticos. •Conocimientos en Industria Médica (dese…
Skills: Microsoft Office, Word, Excel, PowerPoint, Mathematical Calculations
REQUISITOS: •Primaria Concluida. •Conocimiento básico de Office (word,excel,power point). •Capacidad de hacer cálculos matemáticos. •Conocimientos en Industria Médica (dese…
Skills: Microsoft Office, Basic Mathematics, Manual Tool Handling, Assembly, Packing
Abbott
Operario(a) de Producción Abbott B44
Alajuela, Alajuela Province, Costa Rica · On-site
Entry level$20B raised
JOB DESCRIPTION:Operario(a) de Producción Abbott B44 Turno A: lunes a viernes de 6:00am a 3:36pm. Turno B: lunes a viernes de 3:30pm a 10:00pm y sábados de 8:00am a 3:30pm. Turno C: lunes a viernes de 10:00pm a 6:00am. R…
Skills: Medical Device Manufacturing, GMP, GDP, Product Inspection, Line Clearance
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Full-time
bachelor degree
Posted 43d ago
~40 hrs/week
Responsibilities
Perform internal and supplier audits to ensure compliance with government regulations, ISO standards, and company policies. Manage the SCAR and CAPA systems while providing compliance guidance and supporting regulatory submissions like 510K.
Requirements
Requires a bachelor's degree in an engineering discipline and 6-7 years of related experience. Must possess strong knowledge of audit and statistical techniques and the ability to communicate effectively with regulatory agencies.
Full job description
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 XXXXX 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: Performs planned and unplanned internal and supplier audits to verify compliance to applicable government regulations, standards and to company policies and procedures. Maintains Supplier Quality requirements and supports Quality Systems within Confluent Medical such as Training, Customer audits, material nonconformance investigation and Document Control. Recommends improvement to quality systems based on assessments performed. Provides compliance guidance to the organization as required including guidance to lower level personnel. Exercises judgment within defined procedures and practices to determine appropriate action. Participates in decisions on scope of work and length of tasks. Writes, reviews, documents, and implements requirements. Provides and develops solutions to problems. Works independently on routine tasks and needs supervision to resolve some complex issues. Supports administration of the SCAR and CAPA system.
ESSENTIAL DUTIES AND RESPONSABILITIES include the following. Other duties may be assigned.Plans, schedules, conducts, and coordinates detailed phases of engineering work in part of a major project or in a total project of moderate to complex scope.Technically supervises or coordinates the work of engineers, draftspersons, technicians, and others who assist in specific assignments.Performs planned, internal and supplier audits of product and service suppliers for compliance to applicable government and international regulations and company procedures.Assures that the supplier quality system audit function complies with QSR/GMP and ISO requirements.Assigns and owns actions or Corrective actions for deficiencies as needed and required. Drive for completion of actions from nonconformance finding to resolution and disposition.Assigns classifications and documents audit results in written audit reports.Can serve as lead auditor, leading a team of auditors, technical experts and auditors-in-training.Performs Supplier Module administration for ETQ Reliance software.Work with Supply Chain department to maintain supplier profiles up to dateSubject Matter Expert for Supplier Management QSE sectionReviews audit responses and assists with required training in response to audit findings and other GMP/QSR/ISO related issues as needed.Periodically collects compliance metrics and generates data for management reviews.Maintains abreast of regulatory changes through industry publications, seminars, participation in trade organizations, and government meetings.Responsible for following all company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.Support Regulatory Affairs processes, including submission of product 510K and Design Dossier.Ensure Supplier Change Notifications are implemented as planned in Confluent´s systemActs as Quality Manager as required.Leads team efforts to achieve departmental and company goals.
EDUCATION and/or EXPERIENCE: Bachelor degree in engineering discipline; also 6-7 years of related experience. Work requires a broad knowledge of precedents in the specialty area and a good knowledge of principles and practices of relates specialties. Knowledge of audit and statistical techniques is a must.
OTHER SKILLS and ABILITIES: Proficient oral and written English level. Ability to conduct external audits and communicate with external parties. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Ability to use PC's and associated software. Ability to effectively interface with governmental and independent auditors. Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to write speeches and articles for publication that conforms to prescribed style and format. Ability to effectively present information to top management, public groups, and/or boards of directors. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. Ability to define problems, collects data, establishes facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Ability to define problems, collects data, establishes facts, and draw valid conclusions.
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 responsibilitiies
Let our material science technologies and high-performance manufacturing help bring your medical device designs to life.
Industry
Medical Equipment Manufacturing
Company size
1,001-5,000 employees
Founded
1991
Headquarters
Scottsdale, Arizona
LinkedIn followers
47,908
Confluent Medical Technologies applies materials science to MedTech innovation. Confluent specializes in expert design, development, and large-scale manufacturing of 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.
Offices: 6263 N Scottsdale Road, Suite 224, Scottsdale, Arizona 85250, US · 47533 Westinghouse Drive, Fremont, CA 94539, US · 27721 La Paz Road, Laguna Niguel, CA 92677, US · Coyol Free Zone, Building 14, Alajuela, CR · 60 Commerce Drive, Warwick, RI 02886, US
Medical Devices and ComponentsNitinol Component ManufacturingMedical Device Design and DevelopmentFEAFatigue and Corrosion Testing ServicesBalloon Expandable StentsBalloon CathetersBiomedical TextilesGuidewiresAccess Kits
How many Healthcare jobs are open in Alajuela, Costa Rica right now?
There are currently 121 open healthcare positions in Alajuela, Costa Rica listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Alajuela, Costa Rica?
Companies currently hiring include Confluent Medical Technologies, Hologic, Inc., Medtronic, Abbott, Smith+Nephew, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Alajuela, Costa Rica?
Yes — 17 of the 121 open healthcare positions offer remote or hybrid work (0 remote, 17 hybrid).
How do I apply for Healthcare jobs in Alajuela, Costa Rica?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.