Quality Control Lead

Reposted 5 Days Ago
Be an Early Applicant
Alajuela, Alajuela, CRI
In-Office
Senior level
Healthtech
The Role
Organize Quality Control tasks, perform inspections, manage nonconformance reports, and ensure compliance with training and quality standards.
Summary Generated by Built In

Job Description:

SUMMARY: Organize QC tasks and assign resources. Responsible for operating testing services and equipment in the production floor. Perform quality inspection in the production floor as to the incoming material.

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

  • Coordinates tasks related to Quality Control inspections, organizes and assigns resources including allocation of Quality Inspectors to perform daily activities on the production floor.
  • Support to Quality Supervisor by training and assessing technical performance of Quality Inspectors.
  • Support to Quality Supervisor by ensuring that all Quality Inspectors completed required regulatory and on the job training on time.
  • Executes Quality Inspector functions as required due to temporary personnel leaves or work load increments.
  • Opens. reviews and closes nonconformance reports.
  • Routes document revisions in the document control system.
  • Communicates with Manufacturing Leaders and Supervisors to resolve basic to intermediate quality issues.
  • Executes inspections, adjustments, testing and equipment maintenance as required.
  • Manage priorities of closing of lots for exportation
  • Assists engineers with troubleshooting and debugging of processes.
  • 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.
  • Support the Supervisor by ensuring that all Quality Inspectors completed all appropriate quality safety and environmental hazard training, and comply with applicable safety requirements.

SUPERVISORY RESPONSIBILITIES:

Have supervisory responsibilities: No     

Leadership: N/A

Supervises: N/A

Supervision:

General supervision: routine duties are performed with minimal supervision; standard practices or procedures allow proceeding alone at routine work; occasional check of work while in progress; work is reviewed upon completion.

EDUCATION and/or EXPERIENCE: High school degree, with 6-7 years of experience in quality or medical devices industry. Intermediate personal computer skills, including electronic mail, routine database activity, word processing, spreadsheet, graphics, etc.

OTHER SKILLS and ABILITIES:

COMMUNICATION SKILLS:  Assertive communication.

Writes basic technical reports. Actively participates in team meetings.

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively to management or employees of organization levels.

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

Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Demonstrates basic problem-solving skills and ability to deal with problems involving a few concrete variables in standardized situations.

MANUAL DEXTERITY

Manual dexterity sufficient to reach/handle items, works with the fingers, and perceives attributes of objects and materials.

VISION REQUIREMENTS: Ability to adjust focus

WORK SCHEDULE/HOURS: Monday – Friday.

TRAVEL: NONE

ENVIRONMENTAL WORKING CONDITIONS

Well-lighted, heated and/or air-conditioned indoor office setting with adequate ventilation

PHYSICAL DEMANDS

Other physical working conditions:     

Lifting or carrying items.

Moderate noise (examples: business office with computers and printers, light traffic)

PHYSICAL ACTIVITY LEVEL:

Light physical activity performing non-strenuous daily activities of a productive/technical nature.

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.

Skills Required

  • High school degree
  • 6-7 years of experience in quality or medical devices industry
  • Intermediate personal computer skills

Confluent Medical Technologies, Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Confluent Medical Technologies, Inc. and has not been reviewed or approved by Confluent Medical Technologies, Inc..

  • Healthcare Strength Benefits are considered solid, with medical, dental, and vision coverage described positively and HSA-eligible options supported by employer contributions. Feedback suggests core health coverage is a relative bright spot within the total package.
  • Retirement Support A 401(k) with company match is repeatedly highlighted as a positive element. Feedback suggests retirement provisions add meaningful value to total compensation.
  • Fair & Transparent Compensation Compensation is considered competitive in several engineering and managerial tracks, with role-specific pay bands viewed as strong in those paths. Feedback suggests certain professional roles receive competitive pay bands.

Confluent Medical Technologies, Inc. Insights

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The Company
HQ: Scottsdale, AZ
1,068 Employees
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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