Position Details
About this role
This role involves validating computerized systems in a pharmaceutical manufacturing environment, ensuring compliance with regulatory standards, and managing validation lifecycle activities.
Key Responsibilities
- Lead CSV activities
- Ensure regulatory compliance
- Manage validation lifecycle
- Automate validation processes
- Collaborate with manufacturing teams
Technical Overview
The technical scope includes computer system validation, automation processes, regulatory compliance, and lifecycle management within healthcare manufacturing settings.
Ideal Candidate
The ideal candidate is a mid-level validation engineer with experience in computer system validation, regulatory compliance, and pharmaceutical or healthcare environments, with strong attention to detail and teamwork skills.
Must-Have Skills
Nice-to-Have Skills
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of experience in pharmaceutical or healthcare validation, No knowledge of cGMP or validation lifecycle, Inability to work in North Carolina
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