Technical Writer - Packaging – Pharmaceutical Industry
Eurofins Scientific is an international Life Sciences company that offers a wide range of Analytical Services oriented towards the life sciences. Our clients are from very diverse sectors. The Eurofins group is a world leader in the analysis of products ranging from the food we eat, to the water we drink, or the medicines prescribed to us. Eurofins works with the largest companies in the world to ensure that the products they supply are safe, that their ingredients are authentic, and that the labeling is accurate. Eurofins is the world leader in testing food, environmental, pharmaceutical, and cosmetic products, as well as agroscience. It is also one of the leading independent global market leaders in certain laboratory testing and services for genomics, pharmacology discovery, forensics, CDMO, advanced materials science, and clinical study support. In just over 30 years, Eurofins has grown from a laboratory in Nantes, France, to having more than 63,000 employees distributed across a network of more than 1,000 independent companies in more than 60 countries, operating more than 950 laboratories. Eurofins offers a portfolio of more than 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability, and purity of biological substances and products, as well as innovative clinical diagnostic testing services, being one of the main emerging global players in specialized clinical diagnostic testing. In 2025, Eurofins generated total revenues of 7.296 billion euros and has been one of the best-performing companies in Europe over the last 20 years. .
EUROFINS, a leading multinational company providing 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. Reporting to the Manager director, the candidate will be responsible for: Preparing procedures, work instructions, and training materials related to the packaging process in the new packaging lines. Preparing procedures, instructions, and training materials associated with packaging operations modified by the implementation of two new management software. Conversion of current procedures into operating guides. Preparing documentation related to risk analyses (PFMEAs) and production process flows (PFDs) corresponding to the new packaging lines. Coordinating the review and acceptance process of the content with the involved areas. Documentation / Recording of activities and results obtained in computer-based media. Use and data entry in EWM, PharmaSuite, and other company documentary and management systems. Coordinating review sessions, collecting feedback, project milestones, deliverables, and required resources to ensure compliance with deadlines.
Degree or master's 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. Experience in management software such as EWM, PharmaSuite, SAP… will be positively valued. 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.
Immediate start. Indefinite contract. Remote work with presence at the client's site according to project needs. Schedule from Monday to Friday from 07:30-08:30 to 16:00-17:00.