Nr ref.: LP/TR/ZD/08
The individual will work with tech team to author/modify/update system documents as necessary. The person will be working with the Business and Tech Organization to gather and assess existing documents and recommend necessary updates/actions to meet compliance requirements.
The Technical writer will be mainly responsible for assessment and maintenance of system documents.
The individual will perform assessment of existing documents to check for any gaps. The person will provide hands-on assistance to application tech owners in updating appropriate application documents.
We are looking for person who enjoys working with different teams.
Responsibilities:
- Assess existing system documents (system requirements, specifications, reports etc.);
- Work with QA lead to analyze any gaps in system documentation;
- Maintain & update traceability matrix and any other technical system documents as necessary;
- Prepare, review, revise, and maintain technical documents, including software and systems engineering, system operations, testing, and user documentation;
- Write, format, edit, review, and proof procedural and technical information for technical and nontechnical users;
- Gather and analyze technical and product information from various sources to document new or changing product functionality and/or platform;
Requirements:
- Knowledge on GxP and supporting pharma customers;
- Understanding of system categories and related documents;
- Strong communication skills;
- Excellent written and verbal skills in English;
- Ability to update or compose documents;
- Remote work;
- Good time management skills.
Qualifications will be nice:
If you have the following characteristics, it would be a plus but not essential:
- Experience with Veeva VQD or similar Content Management System
- Understanding Pharma or Consumer Healthcare: Quality, Clinical domain, Regulatory, Medical and Safety domain;
- Stakeholder Management Experience