Data Entry Specialist

ZEISS Group

Bogotá ciudad

Presencial

COP 11.160.000 - 17.856.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

ZEISS seeks a Data Entry Specialist in Bogotá, Colombia, to handle medical prescription information with accuracy and care. The role involves transcribing prescriptions, reviewing country-specific requirements, and escalating unclear cases to experts.

Training and continuous improvement are integral to the work, supporting an international workflow. Applicants should demonstrate meticulous data handling, strong computer skills, and a structured approach.

Formación

  • Experience in data entry, transcription, document review, or similar roles.
  • Excellent attention to detail, concentration, and accuracy.
  • Ability to follow procedures and apply specific requirements consistently.
  • Good computer skills and strong organizational abilities.
  • Structured, reliable, and results-oriented approach to work.
  • Written Mandarin: ability to read and interpret Mandarin characters, preferably Traditional Chinese.

Responsabilidades

  • Accurately transcribing information from optical prescriptions.
  • Reviewing documents according to requirements applicable to different countries and regions.
  • Identifying inconsistencies, missing information, or potential errors.
  • Meeting established quality and productivity standards.
  • Escalating complex or unclear cases to the specialized team.
  • Participating in training, quality sessions, and continuous improvement activities.

Conocimientos

Data entry
Attention to detail
Documentation review
Procedural follow-through
Mandarin reading
English proficiency

Descripción del empleo

Data Entry Specialist – Medical Prescription Verification

ZEISS stands for technology and innovation. Founded in Germany in 1846, ZEISS is a global technology leader operating in the fields of optics and optoelectronics across more than 50 countries.

We are currently looking for a Data Entry Specialist to join our team in Bogotá, Colombia.

The position is part of an international operation focused on the management and validation of information related to optical prescriptions received from different global markets.

About the Position

The main purpose of this role is to ensure the accuracy, quality, and proper interpretation of information before processing, while taking into account market-specific requirements.

In this role, you will be responsible for:

  • Accurately transcribing information from optical prescriptions.
  • Reviewing documents according to requirements applicable to different countries and regions.
  • Identifying inconsistencies, missing information, or potential errors.
  • Meeting established quality and productivity standards.
  • Escalating complex or unclear cases to the specialized team.
  • Participating in training, quality sessions, and continuous improvement activities.
What We Are Looking For
  • Experience in data entry, transcription, document review, or similar roles.
  • Excellent attention to detail, concentration, and accuracy.
  • Ability to follow procedures and apply specific requirements consistently.
  • Good computer skills and strong organizational abilities.
  • Structured, reliable, and results-oriented approach to work.
  • Written Mandarin: ability to read and interpret Mandarin characters, preferably Traditional Chinese.
It Would Be an Advantage
  • Experience in document review or validation.
  • Experience working with technical or regulated information.
  • Knowledge of optical prescriptions or related terminology.
  • English proficiency to work effectively in an international environment.

As part of ZEISS, you will have access to:

  • Structured training and professional development.
  • Experience within a global and innovative organization.
  • A collaborative and multicultural working environment.
Additional Information
  • Area: Operations / Data Verification.
  • Scope: International markets.
  • Training: ZEISS will provide the specific training required on applicable regulatory requirements and processes.

Join a global organization where innovation, excellence, and collaboration drive the development of technologies that transform markets and contribute to the progress of society.

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