emagine is seeking a Senior Technical Writer to support a client in the pharmaceutical industry. The consultant will work full-time for 6 months, focusing on updating and streamlining documentation for a digital product in Quality Control (QC). The position requires adherence to GMP standards, ensuring all documents are accurate, compliant, and aligned with the latest software versions.
Key Responsibilities:
Streamline and update existing documentation (SOPs, user guides, training materials) to match the latest software version.
Ensure all documentation complies with GMP quality and compliance standards within QC.
Collaborate with various stakeholders including end-users, developers, data scientists, and SMEs to gather input for updates.
Create a functional structure for documentation and manage updates related to software releases.
Set up a process for efficient future documentation updates.
Manage the Document Change Control (DCC) process.
Skills Required:
Proven experience in writing and managing documents such as SOPs, user guides, and training materials.
Strong understanding of GMP and compliance standards.
Detail-oriented with the ability to maintain a big-picture perspective.
Ability to work efficiently in a fast-paced environment and ask critical questions to meet high-quality standards.
Structured, inquisitive, and problem-solving mindset.
This role is an excellent opportunity for those with expertise in technical writing and quality control processes within GMP environments.
Start Date: 1st November 2024
Duration: 6 months
Work Location: Gentofte, Denmark (Hybrid)
Allocation: Full time
