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קווליטסט
Location: Netanya
Job Type: Full Time
Qualitest is growing and we are looking for our next Validation engineer to join our team in Netanya
As a Validation engineer in the pharmaceutical industry, you will play a crucial role in ensuring that manufacturing processes, equipment, and systems meet regulatory requirements and quality standards. You will be responsible for validating processes and equipment used in the production of pharmaceutical products to ensure their safety, efficacy, and compliance with regulatory guidelines.
As a Validation engineer in the pharmaceutical industry, you will play a crucial role in ensuring that manufacturing processes, equipment, and systems meet regulatory requirements and quality standards. You will be responsible for validating processes and equipment used in the production of pharmaceutical products to ensure their safety, efficacy, and compliance with regulatory guidelines.
Requirements:
* BA/BSc degree or equivalent in Science or Engineering is required, or a technical diploma with practical engineering experience.
* 1 - 2 years experience in the pharma industry
* Required knowledge and experience with equipment utilities validation, preferred knowledge and experience with validation for refrigerators, water systems.
* Knowledge and experience with executes documentation for validation studies ensuring compliance with QA and cGMP systems.
* Knowledge and experience with executing validation protocols IQ, OQ and PQ protocols, Writing IQ, OQ and PQ Reports. Performing and summarizing various annual testing.
* Knowledge and experience with discrepancies, deviations and RC investigations writing required.
* Knowledge of GMPs related to validations for biologics and combination products is preferred.
* Excellent English
* BA/BSc degree or equivalent in Science or Engineering is required, or a technical diploma with practical engineering experience.
* 1 - 2 years experience in the pharma industry
* Required knowledge and experience with equipment utilities validation, preferred knowledge and experience with validation for refrigerators, water systems.
* Knowledge and experience with executes documentation for validation studies ensuring compliance with QA and cGMP systems.
* Knowledge and experience with executing validation protocols IQ, OQ and PQ protocols, Writing IQ, OQ and PQ Reports. Performing and summarizing various annual testing.
* Knowledge and experience with discrepancies, deviations and RC investigations writing required.
* Knowledge of GMPs related to validations for biologics and combination products is preferred.
* Excellent English
This position is open to all candidates.
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