Job Description:

At Confluent, we are committed to our values of teamwork, innovation, accountability, integrity, leadership, and customer focus. We invest in a team that represents these values. Every member of our team plays a critical role in delivering high quality life-saving medical devices. We are the medical device industry's most trusted partner, and we achieve this with an organization focused on safety, efficiency, and customer satisfaction.

We are looking for a Production Clerk 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: Under direct supervision, performs and documents production functions relating to fabrication, modification and assembly of components or finish medical devices.

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

• Performs and documents operations in the production process.
• Performs process/product tests and audits for conformity to quality and/or regulatory requirements.
• When applicable, follows standard operating procedures for all tasks.
• Maintains clean and orderly work area.
• Has completed all appropriate safety and environmental hazard training.
• Responsible for ensuring personal and company compliance with local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
• Responsible for Epicor transactions between warehouses and the production floor and revise documentation regarding material receipts and the corresponding Epicor transactions.
• Collaborate with Quality system.

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. 2-3 years of related experience. Intermediate personal computer skills, including electronic mail, routine database activity, word processing, spreadsheet and graphics.

OTHER SKILLS and ABILITIES: Ability to read and understand technical documentation associated with specific discipline. Must be able to successfully complete company/department training courses in manufacturing techniques. Ability to learn regulatory (GMP) requirements.

Ability to read and comprehend simple instructions, short correspondence, and memos. Ability to write simple correspondence.

Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.

MANUAL DEXTERITY: Manual dexterity sufficient to work with the fingers.

VISION REQUIREMENTS: No special vision requirements

WORK SCHEDULE/HOURS: Monday – Saturday.

TRAVEL: N/A

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

PHYSICAL ACTIVITY LEVEL:

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

COMMENTS:  This job 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. Other related job objectives, special assignments and less significant responsibilities will typically be performed by the incumbent(s).