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Senior Technical Writer iSens Porto

Abbott


Job Location:

Porto - Portugal

Monthly Salary: Not provided by the employer
Posted: 2 August 2026 (30+ days ago)
Application Deadline: 30 October 2026
Vacancies: 1 Vacancy

Job Summary

JOB DESCRIPTION:

Responsible for writing and editing technical documents including requirements documents specifications design history files verification and validation protocols.

Creating clear concise and accurate documentation that supports the companys products and services. This role ensures that complex technical information is translated into user-friendly content for various audiences including developers customers and internal teams.

The Technical Writer will collaborate closely with product managers engineers and subject matter experts to maintain high-quality documentation that enhances user experience and product adoption.

MAIN RESPONSIBILITIES

  • Develop and maintain technical documentation including user guides API references FAQs and release notes.
  • Translate complex technical concepts into clear accessible language for different audiences.
  • Ensure documentation aligns with brand standards and follows best practices for structure and readability.
  • Reviews Design Control documentation to assess compliance to processes and procedures and works with teams to address and correct deficiencies.
  • Participates in product/process improvement troubleshooting complaint handling and customer support.
  • Technical Writing: Write and edit technical documents including requirements documents specifications verification and validation documents Failure Modes and Effects Analysis (FMEA) documents Design Planning documents Design Review records.
  • Convert relevant product data and information into a form that meets Quality and submission requirements.
  • Review circulate edit assemble inspect and duplicate reports and documentation.
  • The documents written and managed will be used throughout the product life cycle for on-market and future products.
  • The output provided by the incumbent/candidate is subject to external audit (e.g. ISO). The lack of accuracy and timeliness will impact the Quality system at site and division levels.

QUALIFICATIONS

Education

Bachelors Degree Science Medical Technology or equivalent technical degree or an equivalent combination of education and work experience

Experience/Background

Minimum 3 years

Relevant experience in a related area such as R&D Technical Product Development or Quality in a healthcare industry.

Writing editing and managing technical documentation utilized in the development of new products and improvement of existing products.

Good written and oral communication skills.

The base pay for this position is

N/A

In specific locations the pay range may vary from the range posted.

JOB FAMILY:
IT Services & Solutions Delivery

DIVISION:
CRLB Core Lab

LOCATION:
Portugal > Porto : Rua Orlando Ribeiro No. 78 Leça do Balio

ADDITIONAL LOCATIONS:

WORK SHIFT:
Standard

TRAVEL:
No

MEDICAL SURVEILLANCE:
Not Applicable

SIGNIFICANT WORK ACTIVITIES:
Not Applicable


Required Experience:

Senior IC


About Company

Company Logo

WHO WE ARE CREATING LIFE-CHANGING TECHNOLOGY From removing the regular pain of fingersticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s ... View more

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