Location
- Philippines
Category
The role
Validation plans, requirement specifications, migration reports and SOPs for regulated pharma software make up the bulk of your workload, with Confluence holding customer-facing FAQs, knowledge base articles and onboarding content. You need two years of software technical writing and cGxP experience, preferably in pharmaceuticals. It is a remote, full-time role for people based in the Philippines, and training runs on U.S. working hours.
At a glance
- Experience
- 2+ years
- Level
- Mid-level
Tools and skills
Tools
Skills
Regulatory DocumentationStandard Operating ProceduresTechnical DocumentationProcess DocumentationTechnical Writing

