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 Supervisor II 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: Manufactures products and carries out supervisory responsibilities in accordance with the organization´s policies and applicable labor law; organizing and monitoring work flow.
ESSENTIAL DUTIES AND RESPONSABILITIES
EDUCATION and/or EXPERIENCE: Bachelor degree in business administration, engineering or other related is required, with 2-3 years of related experience. Alternatively, high school diploma plus 6 years of additional experience in similar roles in medical industry. Proficient personal computer skills including electronic mail, record keeping, routine database activity, word processing, spreadsheet and graphics.
SUPERVISORY RESPONSIBILITIES:
Have supervisory responsibilities: Yes
Leadership: Provide unlimited supervision to others through motivation, direction, review and feedback of assigned tasks.
Supervision:
Immediate supervision: receive close supervision related to specific work activities, assignments and methods usually receive frequent surveillance over job activities; instructions are detailed and assignments are typical short-term.
Supervises:
OTHER SKILLS and ABILITIES: Ability to lead and manage self-directed work team. Ability to audit production areas identify non-compliance to requirements, and develop/oversee action plans for corrective action. Extensive knowledge in matters such as labor relations, labor law regulations, manufacturing methods, production planning and assembly activities. In depth understanding of production and quality control techniques such as CFM, JIT.
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 before groups of customers or employees of organization.
Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume.
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
MANUAL DEXTERITY: Manual dexterity sufficient to reach/handle items and work with the fingers.
VISION REQUIREMENTS: Ability to adjust focus (ability to adjust the eye to bring an object into sharp focus)
WORK SCHEDULE/HOURS: Monday – Saturday.
TRAVEL: Minimal
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:
Sedentary physical activity performing non-strenuous daily activities of an administrative nature.
COMMENTS: This position 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 incumbents(s) will typically perform other related job objectives, special assignments and less significant responsibilities.