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Validation And Technical Documentation Writer - Remote
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Full-time
Remote
- PharmaLogic is the fastest-growing SPECT & PET radiopharmaceutical solutions provider and contract development and manufacturing organization (CDMO) with radiopharmacies across North America.
- We are passionate about expanding the power of radiopharmaceutical technology to provide transformative diagnostic and therapeutic agents to patients from bench to bedside.
- The Validation and Technical Documentation Writer will play an essential role in generating Standard Operating Procedures (SOPs), Validation Protocols, and Technical Reports to uphold regulatory compliance and ensure the quality and safety of radiopharmaceutical manufacturing processes.
- Develop and maintain detailed Standard Operating Procedures (SOPs), Protocols, and Technical Reports for validation activities within a Radiopharmaceutical manufacturing environment.
- Experience in a GMP, GLP, or GCP environment is preferred.
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