Commissioning & Qualification Documentation Lead
Stark Pharma Solutions Inc · Lebanon, IN · 2 mo ago
On-siteAdministrativeFull-time
Key Responsibilities
- Independently draft, write, and develop commissioning and qualification documentation from initial concept through final approval, including protocols, reports, and supporting records.
- Author and manage CLIAs (change controls) related to commissioning and qualification activities, ensuring alignment with site procedures and regulatory expectations.
- Lead negotiations and technical discussions with external vendors to resolve documentation, scope, and execution-related issues.