Assignment Description

We are looking for a Technical writer with a focus on IT-projects to our client.

Tasks:

• Responsible for turn over package and support business with high quality and easily available technical information.
• Prepare and maintain the technical documentation package and ensure compliance, training, and alignment.

Key responsibilites:

• Quality control of all documentation to ensure compliance with rules and regulations.
• Make sure that the turnover package is according to the GMP/GDocP.
• Expedite factories and other stakeholders to supply documentation.
• Collaborate with Design/Automation/Electrical engineers, Project managers and Product supply team on daily basis.
• Cooperate with customers (as well) regarding to the turnover package requirements and deliverables.

Who you are:

• Detail-oriented, perseverant, strong communication skills, and adept at collaborating within a team environment.
• Experience in documentation management within the pharmaceutical or biotechnology sectors is highly desirable, given the diverse range of pharmaceutical clientele.
• Proficiency in English is essential, and knowledge of Swedish is advantageous.

The consultant must be able to work 4 days onsite.