Technical Writer

Category: Manufacturing

Location:Odense, Region South Denmark, DK

• Participating in activities such as development of training plans, standard operational procedures, job instructions, risk management, regulatory impact assessment and implementation plans.

• Supporting, executing and coordinating validation of processes in project/small changes as Technical Writer.

• Providing support for development on manufacturing changes, line extensions, compliance with, and interpretation of applicable regulations.

• Ensuring documentation meet regulatory requirements and ensure timely approval of internal documents and procedural changes.

• Independently addressing daily tasks within the work area, including working proactively with quality and collaborating across Novo Nordisk department to achieve optimal solutions.

• Participating in problem solving and active use of c LEAN tools in daily life, audits and inspections.

• Contributing to process improvement as a Technical Writer and within project teams, and participating in process improvements and implementation.
  
  

• BSc/MSc education within natural or technical science, such as mechanical, manufacturing engineer or related field. As a minimum, it is required to have a technical education.

• 2 years of experience in the pharmaceutical or biotechnology industry.

• Experience working within a production area and familiarity with electronic records.

• Good Communication skills, and ability to create transparency for colleagues in own team.