Costa Rica Job Openings
Establishment Labs
Supervisor de Manufactura Turno C (Domingo a Sabado 10:00pm a 6:00am)
FULL TIME
September 14, 2024
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.
Work Schedule available: Sunday to Saturday from 10:00pm to 6:00am
About the Role:
Plan, coordinate and execute all activities required to ensure compliance with manufacturing indicators and
company goals avoiding any production delays and/or optimizing the production processes.
This includes managing manufacturing resources and capacity, ensuring compliance with quality and regulatory
requirements, maintaining a safe working environment and leading a team of manufacturing personnel.
The supervisor collaborates with other departments, such as Engineering, Supply Chain, and Quality, to address
quality-related issues, implement process improvements, and ensure alignment with organizational goals and
objectives.
Main Responsabilities:
Job Requirements:
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.
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.
Work Schedule available: Sunday to Saturday from 10:00pm to 6:00am
About the Role:
Plan, coordinate and execute all activities required to ensure compliance with manufacturing indicators and
company goals avoiding any production delays and/or optimizing the production processes.
This includes managing manufacturing resources and capacity, ensuring compliance with quality and regulatory
requirements, maintaining a safe working environment and leading a team of manufacturing personnel.
The supervisor collaborates with other departments, such as Engineering, Supply Chain, and Quality, to address
quality-related issues, implement process improvements, and ensure alignment with organizational goals and
objectives.
Main Responsabilities:
- Ensuring a safe working environment for all employees.
- Comply with the confidentiality contract and maintain integrity.
- Supervise, guide, and motivate the operative personnel including the manufacturing leader and Record Keeper.
- Ensure that all products manufactured in manufactured in the areas in charge meet quality and regulatory requirements.
- Management of manufacturing indicators
- Participate in the implementation of key projects of the company (improvements, new products, and new processes projects)
- Identify process improvements and promote a continuous improvement culture.
Job Requirements:
- Bachelor’s degree in applied science such as Production, Industrial Engineering, Chemical Engineering or other related area or equivalent experience.
-
Knowledge of manufacturing processes.
Knowledge of ISO 9001, ISO 13485, FDA, CE Mark standards. - Computer knowledge is required: spread sheets, word processor, other utilities, basic knowledge of commercial software package (i.e. Windows or similar) and basic computer configuration.
- Experience in controlled production environments.
- SAP or similar knowledge.
- Intermediate English
-
From one (1) to two (2) years of experience working in manufacturing positions in medical industry or 3 years in other industries.
Knowledge of manufacturing processes.
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.
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