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Technical Writer - Manufacturing

Hybrid in Madrid·Full-time·Added yesterday

Still open when we checked on 8 Oct

Eurofins

47 open roles

Overview

Job details

  • Permanent contract

    Full-time.

  • Hybrid

    Office and home days — the ad has the split.

Requirements

  • Have the right to work in Spain

    Eurofins doesn't mention sponsorship in the ad.

  • Work in English

    English is required, per the ad.

  • Be near Madrid, Spain (Hybrid) for hybrid days

    No relocation package mentioned.

  • Have 2+ years of experience

    Mid-level role.

  • University degree

    “Graduado o máster en Química, Biología o similar.” — per the ad.

Skills

This job advert was originally written in Spanish.

Requirements

What we're looking for

  • Graduate or Master's degree in Chemistry, Biology, or similar.
  • Minimum of 2 years of experience in a GMP/GLP environment.
  • Minimum of 2 years of experience in a similar position in the pharmaceutical or related industry.
  • Minimum of 3 years of experience in technical writing in GMP or industrial environments.
  • A very responsible, careful, clean, and organized person, with technical capacity for organization and workload management, with ease of integration and teamwork, as well as autonomy for individual work.
  • High level of English.

Nice to have

  • Experience in management software such as EWM, PharmaSuite, SAP… will be positively valued.

The role

EUROFINS, a leading multinational company offering specialized laboratory services to the pharmaceutical sector, is selecting a Technical Writer to join a large project carried out at the facilities of a pharmaceutical company located in Madrid.

What you'll do

Reporting to the Director Manager, the candidate will be responsible for:

  • Drafting the procedures, work instructions, and training materials related to the packaging process in the new packaging lines.
  • Drafting the procedures, instructions, and training materials associated with the packaging operations modified by the implementation of two new management software systems.
  • Conversion of current procedures into operating guides.
  • Drafting the documentation related to risk analyses (PFMEAs) and production process flows (PFDs) corresponding to the new packaging lines.
  • Coordinating the content review and acceptance process with the involved areas.
  • Documentation / Recording of activities and results obtained in computer-based formats.
  • Utilization and data entry in EWM, PharmaSuite, and other company documentary and management systems.
  • Coordinating review sessions, gathering feedback, project milestones, deliverables, and required resources to ensure compliance with deadlines.

About Eurofins

Eurofins Scientific is a global leader in laboratory testing and services, providing a comprehensive range of analytical procedures to ensure the safety, authenticity, and quality of products across industries such as food, pharmaceuticals, environment, and consumer products. With over 60,000 employees and more than 900 laboratories worldwide, the company operates as a decentralized network of specialized labs, offering services from routine testing to cutting-edge research and development.

In Spain, Eurofins has a significant presence with multiple laboratories and offices across the country, including in Madrid, Barcelona, and other regions. The company is known for its scientific excellence and offers a dynamic, international work environment. For international professionals, Eurofins provides opportunities to work in a truly global organization with diverse teams, and many roles require English proficiency, making it accessible for non-Spanish speakers. The company emphasizes continuous learning and career development, with many positions in laboratory analysis, quality assurance, and regulatory affairs.

Industry
Lab Services
Founded
1987
Employees
50,000–100,000
Headquarters
Luxembourg City, Luxembourg
In Spain
Madrid, Barcelona

Good to know if you are moving

  • Eurofins is a global company with operations in over 60 countries, offering international career opportunities and potential for cross-border mobility.
  • Many roles in Spain require English proficiency, and some positions are open to non-Spanish speakers, making it accessible for international professionals.
  • The company invests heavily in R&D and innovation, providing a stimulating environment for scientists and technical professionals.
  • Eurofins has a decentralized structure, meaning employees often work in specialized labs with a strong focus on quality and compliance.
  • Spain is a key market for Eurofins, with multiple laboratories and offices, particularly in Madrid and Barcelona, offering a range of roles from lab analysis to regulatory affairs.

In their own words

About the company & team

Eurofins is an international life sciences company offering a wide range of analytical services to clients across diverse sectors. The Eurofins group is a world leader in testing food products, environmental samples, pharmaceuticals, and cosmetics, as well as providing CRO services to the agro-science sector. It is also one of the global leaders in certain laboratory analyses and services for genomics, drug discovery, forensics, CDMO, advanced materials science, and clinical research. Furthermore, Eurofins is one of the emerging companies specialized in clinical diagnostic testing.

In 2025, Eurofins generated €7.2965  million in pro forma revenue, with 950 laboratories distributed across 59 countries and  more than 63,000 employees.

Additional information

  • Immediate start.
  • Permanent contract.
  • Remote work with presence at the client's site according to project needs.
  • Schedule from Monday to Friday, 07:30-08:30 to 16:00-17:00.
All open roles at Eurofins

Location

Eurofins · Madrid

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