Quality Engineering Technician - Horario de Lunes a viernes de 7:30a.m a 5: at Establishment Labs
PDA, Provincia Alajuela, Costa Rica -
Full Time


Start Date

Immediate

Expiry Date

15 Jul, 25

Salary

0.0

Posted On

15 Apr, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Citizenship, Visio, Powerpoint, Excel, Gmp, It, Certified Quality Technician

Industry

Pharmaceuticals

Description

ABOUT US:

Establishment Labs is changing the medical device, breast health, aesthetics and reconstruction industry by designing, developing, and manufacturing an innovative portfolio of advanced medical aesthetic device technologies and wellness solutions. It is currently the world’s fastest-growing women’s health company.
Our Femtech solutions are proudly produced at two MDSAP-certified, carbon neutral, LEED Gold certified, state-of-the-art manufacturing facilities in Costa Rica and are approved for sale in more than 85 countries.
Since 2018 the company trades on the NASDAQ stock exchange under the ticker symbol ESTA and has a market cap of around $1.8 billion.
This is an exciting opportunity to join an innovative international company in hyper-growth as we launch a significant revolution to transform the women´s aesthetics industry.

MAIN RESPONSABILITIES:

  • Support continuous improvements and opportunities for change in QE processes.
  • Ensure compliance with compliance with appropriate regulatory, quality requirements and company policies.
  • Support the Quality Engineering area.
  • Supports engineers in the developing, writing, execution and reporting of validation efforts such as Computer System Validation.
  • Executes protocols for validation, qualifications, and computer software.
  • Investigates and researches equipment, process, computer software to develop protocols to confirm by examination and provision of objective evidence that they consistently produce a result or product meeting its predetermined specifications.
  • Supports SAP implementation and sustaining activities.
  • Project & Computer software validation documentation assistant.
  • All other functions inherent to the position and those assigned by their immediate superior.

JOB REQUIREMENTS:

  • Advanced student in Engineering or related fields in process (50%) or certified quality technician completed.
  • Knowledge of GMP’s (Good Manufacturing Practice).
  • Office package, Excel, PowerPoint, Project Manager, Visio.
  • Intermediate English.
  • 2 years’ experience on roles in the medical devices industry.
    Important Note: This job description includes the necessary aspects required to evaluate this job position. It should not be used as a comprehensive list of all responsibilities, skills or functions.
    At Establishment Labs we’re committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability (visible and not visible), gender, gender identity or expression, or veteran status. We strive to be a more equal opportunity workplace
Responsibilities

Please refer the Job description for details

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