Job Summary
A company is looking for a Change Control Document Management Specialist.
Key Responsibilities
- Manage the development and implementation of specifications for clinical and commercial raw materials
- Interface with cross-functional teams and raw material suppliers to ensure compliance and efficiency
- Act as a change owner within the Change Control Management System to document changes to global documents
Required Qualifications
- Degree in Life Science or Engineering (e.g., Biochemistry, Analytical Chemistry, Biology)
- Preference for candidates with advanced degrees or industry experience
- Project management experience
- Experience in GMP controlled document management
- Knowledge of ERP Systems (SAP)
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