11 Ofertas de del Monte Foods en Costa Rica

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 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 a Quality Control Lead 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: 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 to Friday (Shift A)

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.

JOB TITLE: 
Quality Control Coordinator

Location:
Heredia, Costa Rica

JOB ROLE

To ensure that products, services, and processes meet or exceed established quality standards, aiming for customer satisfaction. This involves developing and implementing quality assurance systems, conducting audits, and collaborating with various departments to achieve optimal quality outcomes.

KEY RESPONSIBILITIES

• Lead the operational quality teams across all business units, ensuring effective collaboration and execution of quality strategies. Conduct performance evaluations and support career development in coordination with the Quality Manager.
• Coordinate the deployment and monitoring of control plans on production lines, ensuring compliance and validating effectiveness through performance data analysis.
• Lead investigations of critical process and product failures using structured problem-solving tools (e.g., 5 Whys, Ishikawa, DOE, FMEA). Ensure timely execution of corrective and preventive actions.
• Oversee and validate NPI activities, including PPAP submissions, internal validations, and compliance with technical specifications.
• Manage the disposition of non-conforming materials, including risk assessments, rework flow definitions, and cross-functional communication.
• Coordinate process and product changes, ensuring proper validation and updates to technical documentation.
• Track and report key quality indicators (e.g., CoPQ, defects, scrap, customer complaints) to support data-driven decision-making.
• Assist the Quality Manager in internal and external audits, including documentation preparation, audit execution, and follow-up on findings.
• Serve as a mentor to Quality Engineers, providing guidance on complex analyses, standards interpretation, and professional growth.
• Actively participate in and lead projects focused on continuous improvement and Lean Manufacturing to enhance operational efficiency.
• Ensure adherence to applicable standards (ISO 9001, IATF and internal policies related to quality, safety, occupational health, and environmental management.
• Organize regular meetings with the quality team to review project status, performance metrics, and issue resolution.

QUALIFICATIONS:

• Bachelor's degree in Engineering (Mechanical, Electronic, Industrial, or Chemical).
• Over 6 years of experience in quality assurance and manufacturing operations with proven experience on people management
• Proficient in ISO 9001 and IATF 16949 standards, with practical application in manufacturing environments.
• Strong understanding of manufacturing processes, including assembly, testing, and process control.
• Continuous Improvement: Skilled in Lean Manufacturing principles and Six Sigma methodologies for process optimization and defect reduction.
• Statistical analysis and process capability studies.
• SAP ERP: Quality module and production data management.
• Microsoft Office Suite: Advanced use of Excel, Word, PowerPoint, and Outlook for reporting and communication
• English level B2+ or higher (CEFR).

Please follow the link in this job posting for more information and to apply.

As a Senior Quality Control Specialist, you are a strong communicator and trusted advisor who partners with Producers, Design Supervisors, Production Designers, Studio Artists, and Technical Artists to guarantee flawless delivery of creative assets. You take ownership of mitigating risks, establishing QC best practices, and ensuring consistent excellence across multiple projects. Your organizational and leadership skills allow you to balance detail-oriented reviews with a high-level perspective of production workflows.

Working as part of the content creation department, you provide strategic oversight and guidance on quality control throughout the entire production lifecycle—from project initiation to final archival. You bring senior-level expertise to complex deliverables, including large-scale video campaigns, mobile applications, interactive platforms, static creatives, HTML banners, and a wide range of digital products. You thrive in the fast-paced world of advertising, helping the team anticipate and avoid issues while raising the overall quality standard.

You will

• Oversee production compliance with standards, technical specifications, and brand guidelines.
• Conduct advanced QC checks for copy alignment, spelling, design consistency, and technical accuracy.
• Proactively identify risks in workflows and propose process improvements to minimize recurring errors.
• Deliver clear, detailed reports and present findings to stakeholders, including senior leadership.
• Represent QC in strategic meetings with producers, design supervisors, and clients when needed.
• Monitor JIRA, inboxes, and communication channels, prioritizing tasks to meet tight deadlines.
• Report project status to leadership and advise on QC resource planning.
• Mentor junior QC team members and share knowledge of best practices in production/post-production.
• Oversee final file preparation, catalog organization, and archival in collaboration with Asset Management.
• Contribute to the continuous refinement of QC processes, tools, and documentation across teams.

You have

• Advanced English level (C1 preferred in reading, writing, and conversation).
• 5+ years in advertising agencies, creative production, or post-production studios.
• Proven ability to lead QC efforts across multiple concurrent projects.
• Strong communication and negotiation skills when addressing quality issues with stakeholders.
• Expertise in video and audio editing tools (DaVinci Resolve, Premiere).
• Broad proficiency with Adobe Suite (Photoshop, After Effects, Illustrator).
• Deep understanding of asset delivery specifications, exporting standards, and cross-platform requirements.
• Strong organizational and cataloging skills with mastery of file-naming conventions.
• A refined eye for design principles and exceptional attention to detail.
• Bachelor's degree in Design, Media Production, or a related field preferred.
• Experience mentoring or training team members is a plus.

What We Offer

• Maternity and parental leave extra days
• Competitive benefits packages
• Vacation, compassionate leave, sick days, and flex days
• Access to online services for families and new parents
• Diversity and Inclusion Board with 12 affinity groups
• Internal learning and development programs
• Enterprise-wide employee discounts
• And more…

At Critical Mass, we value our employees and offer competitive compensation and benefits packages. If you're looking for a challenging and rewarding opportunity to make a significant impact on the lives of our employees, we encourage you to apply for this exciting position today
The Talent Team at Critical Mass is focused on ensuring we provide the best training, onboarding, and employee experience possible Our new hires & employees are the future of our organization, and we want to set you up for long-term success.
This is a 100% on-site role.
The Ask Stems From Our Want To
Strengthen opportunity for continuous learning
Improve collaboration and team relationships.
Increase employee engagement
This work model balances the need for individual flexibility while maintaining the relentless customer focus we provide at CM. We understand that not everyone may feel comfortable with this expectation, so we ask that you please let us know immediately if there are any concerns so we can help navigate accordingly.
Critical Mass is an equal opportunity employer.
The Critical Mass Talent Acquisition team will only communicate from email addresses that use the URLs , and us.greenhouse-
We will not use apps such as Facebook Messenger, WhatsApp, or Google Hangouts for communicating with you.
We will never ask you to send us money, technology, or anything else to work for our company. If you believe you are the victim of a scam, please review your local government consumer protections guidance and reach out to them directly.
*If U.S. based:

If Canada based:

If U.K. based:

If Costa Rica based: *

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 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 a Quality Control Lead senior 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: 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: Yes

Leadership: Yes

Supervises:

• Quality Control Inspector
• Quality Control Lead

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 8+ 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 to Friday (Shift A)

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.

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 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 a Quality Control Inspector 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: Works on most assignments with instructions about the general results expected. Performs mechanical, developmental or test technician duties in such areas as: manufacturing, quality, or engineering, where some judgment, calculations and recording is required. Inspection, adjustments, testing and equipment maintenance is required.

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

• Opens reviews and closes nonconformance's reports.
• Responsible for operating testing services and equipment in the production floor.
• Conducts in process inspections and final inspections as required per inspection plans.
• Executes documentation review for accuracy, completeness for product release, closing of job travelers and issuance of product Certificate of Compliance
• Uses company records systems to perform product data searches.
• Enters data into data collection system (Servoy).
• Execute work assignments assigned by Quality control Inspection Leader or QC Supervisor.
• 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.
• Responsible for completing all appropriate quality safety and environmental hazard training and complying with applicable safety requirements.

SUPERVISORY RESPONSIBILITIES

Have supervisory responsibilities: No

Leadership: Supervise in both their work assignments and performance development (appraisal).

Supervises N/A

Supervision:

Immediate supervision: receive close supervision related to specific work activities, assignments, methods, etc; usually receive frequent surveillance over job activities; instructions are detailed and assignments are typical short-term.

EDUCATION and/or EXPERIENCE: Middle school approved, also 4-5 years of experience in quality or medical devices industry, preferably studies in industrial engineering.

Intermediate personal computer skills, including electronic mail, routine database activity, word processing, spreadsheet, graphics, etc.

OTHER SKILLS and ABILITIES

COMMUNICATION SKILLS: Assertive communication.

Actively participates in team meetings.

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.

Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions.

Ability to use calibrated measurement equipment

Being an innovative person at work

Follow the company values

Requires moderate supervision

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 to Friday (3:30 pm - 9:55 pm) & Sabados (7:00 - 3:00 pm)

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.

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 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 a
Quality Control Inspector I for shift A
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:
Works on most assignments with instructions about the general results expected. Performs mechanical, developmental or test technician duties in such areas as: manufacturing, quality, or engineering, where some judgment, calculations and recording is required. Inspection, adjustments, testing and equipment maintenance is required.

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

• Opens reviews and closes nonconformance's reports.
• Responsible for operating testing services and equipment in the production floor.
• Conducts in process inspections and final inspections as required per inspection plans.
• Executes documentation review for accuracy, completeness for product release, closing of job travelers and issuance of product Certificate of Compliance
• Uses company records systems to perform product data searches.
• Enters data into data collection system (Servoy).
• Execute work assignments assigned by Quality control Inspection Leader or QC Supervisor.
• 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.
• Responsible for completing all appropriate quality safety and environmental hazard training and complying with applicable safety requirements.

Supervisory Responsibilities
Have supervisory responsibilities: No

Leadership:
Supervise in both their work assignments and performance development (appraisal).

Supervises
N/A

Supervision:
Immediate supervision: receive close supervision related to specific work activities, assignments, methods, etc; usually receive frequent surveillance over job activities; instructions are detailed and assignments are typical short-term.

EDUCATION and/or EXPERIENCE:
Middle school approved, also 4-5 years of experience in quality or medical devices industry, preferably studies in industrial engineering.

Intermediate personal computer skills, including electronic mail, routine database activity, word processing, spreadsheet, graphics, etc.

OTHER SKILLS And ABILITIES
COMMUNICATION SKILLS: Assertive communication.

Actively participates in team meetings.

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.

Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions.

Ability to use calibrated measurement equipment

Being an innovative person at work

Follow the company values

Requires moderate supervision

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 to Friday (6:00 - 3:30pm)

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.

Job Description
Performs inspections at various stages of production of the product from raw materials, sub-assemblies and final assemblies to assure quality and conformance to specifications and procedural requirements.

Qualifications
Minimum 1 year experience in medical device manufacturing. High School diploma or equivalent. Good reading and written communication skills

Posting Country
Outside US