
Pharmaceutical Process Validation Specialist
23 hours ago
The successful candidate will be responsible for ensuring the compliance and integrity of our GxP manufacturing processes, systems, and equipment in accordance with EU regulations and internal standards.
This will involve developing and executing validation protocols (IQ/OQ/PQ), conducting risk assessments, and performing periodic reviews of GxP manufacturing processes, equipment, instruments, and computer systems.
The candidate will also be expected to collaborate with cross-functional teams, including production, logistics, sales, and customer service to address GxP requirements, and participate in changes and new projects as needed.
In addition, the candidate will support audits and other quality-related activities to ensure the quality and safety of our products.
Requirements- Bachelor's or Master's degree in a relevant field such as Pharmacy or a related discipline from an accredited university recognized in Norway.
- Experience from GxP or validation in the pharmaceutical industry is an advantage.
- Excellent knowledge of Norwegian and English, both oral and written.
- Strong analytical and problem-solving skills, with a solution-oriented approach.
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