Master information

Task description and requirements

We are currently looking for a CSV expert. Experience in experience in Governance, risk management & compliance and process development is needed.

Enclosed the project details:

Subject Matter Expert - CSV & Compliance (m/f/d)

General information
Reference: 172187
Location: remote
Start: 06.01.2025
Volume: full-time 80-100%
Duration: 3-4 months
Languages: English

Your Skills
- Deep knowledge of pharmaceutical regulatory standards
- Ability to coordinate tasks such as validations, IT controls, and security measures
- Capable of conducting training sessions for internal teams and consultants

Your Tasks
- Act as the Single Point of Contact (SPOC) for auditors regarding IT systems
- Provide and approve all required IT-related documentation
- Ensure data integrity and validation evidence
- Deliver training sessions on CSV
- Support the documentation and verification of IT controls and security measures

Interested?
We look forward to receiving your application documents in electronic form.

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