Job Description:
Mandatory:-
'- Understanding of SDLC and experience with drafting various SDLC document types (CS, DS, RS, Scripts, QASR)
- Specific hands-on experience with validating, qualifying, and/or using Pharmaceutical GMP QC Lab COTS systems are required
4+ years of experience working as a SDLC documentation consultant
Experience with the Software Development Life Cycle, requirements gathering, development, and documentation
Experience with user acceptance testing, use cases and overall testing
Well organized and consistently delivers on commitments
Able to work under tight timeframes and be able to multi-task effectively
* Pharma industry experience is must
• Excellent communication and written skills are required
• Knowledge of manufacturing application & operations
Preferred Skills
• Experience in Labware, Empower LIMS systems
• Experience in validating Lab equipments.
Job Roles/Responsibilities:-
Writes and edits software documentation, including user guides for software applications, reference guides, release notes, and other product-related materials.
Collaborates with developers, analysts, project managers, and client services members to gather documentation requirements for product release notes.
Reviews source materials to ensure delivery of accurate information.
Updates product help system, maintaining and updating content such as instructions, screenshots, workflow diagrams, and video tutorials as needed.
Translates complex and technical ideas and processes into accurate and easily digestible document