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Validation Specialist in Pharmaceutical Engineering
vor 3 Monaten
We are seeking a **Validation Specialist** who will be responsible for ensuring the qualification and validation of machinery and equipment within the pharmaceutical industry. This role involves working at our facilities as well as at client sites.
Key Responsibilities- Performing **qualification and validation** of equipment in compliance with industry standards.
- Preparing essential documentation, including **GMP risk assessments** and various test plans (DQ, IQ, OQ, PQ).
- Facilitating and conducting **workshops** for clients to enhance understanding and compliance.
- Providing **regulatory support** for ongoing development projects.
- Creating comprehensive **test and validation plans**, assisting in their execution and evaluation.
- Offering **consulting services** both internally and externally, including training sessions and workshops.
- Developing innovative **concepts and strategies** to improve validation processes.
- A degree in **mechanical engineering**, **electrical engineering**, or **pharmaceutical technology**.
- Experience in **regulated environments** with a focus on qualification and validation processes.
- Strong **technical knowledge** and analytical capabilities.
- Excellent **communication** and **teamwork** skills, with a methodical approach to tasks.
- Fluency in **German** (both written and spoken) and a good command of **English**.
- Willingness to **travel internationally** as required.
