Technical Writer - Manufacturing – Industria farmacéutica

Eurofins, a leading multinational company specializing in laboratory services for the pharmaceutical sector, is seeking a Technical Writer to join a significant project at a pharmaceutical facility in Madrid. This role involves collaborating with various teams to develop comprehensive documentation that supports manufacturing processes and ensures compliance with industry standards.

The Technical Writer will be responsible for creating procedures, work instructions, and training materials related to the packaging processes of new packaging lines. Additionally, the role includes developing documentation for packaging operations modified by the implementation of new management software, converting existing procedures into operational guides, and preparing risk analysis documents (PFMEAs) and production flow diagrams (PFDs) for the new packaging lines. Coordinating content review and approval processes with involved areas, documenting activities and results in digital formats, and entering data into systems like EWM and PharmaSuite are also key responsibilities.

Candidates should possess a degree or master's in Chemistry, Biology, or a related field, with a minimum of two years' experience in GMP/GLP environments and at least two years in a similar role within the pharmaceutical industry. A minimum of three years' experience in technical writing in GMP or industrial settings is required. Proficiency in management software such as EWM, PharmaSuite, or SAP is advantageous. The ideal candidate will be highly responsible, meticulous, organized, and capable of managing workloads effectively, integrating well into teams, and working autonomously. A high level of English proficiency is also necessary.

The position offers immediate incorporation with a permanent contract. While the role primarily involves remote work, presence at the client's site is required based on project needs. Working hours are Monday to Friday, from 07:30-08:00 to 16:00-16:30.