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12861 - Validation Engineer

Date:  May 1, 2024
Company:  Qualitest Group

Qualitest, the World’s Leading AI-Powered Quality Engineering Company

 

At Qualitest we're all about ensuring everything runs smoothly, whether it's your business, technology, or operations. We leverage smart engineering-led practices and precise processes to maintain excellence in all that we do.

Our clients are the world’s top brands and our diverse global team of 8,000 employees, including 1,500 in Israel, collaborates with industry leaders in technology, finance, insurance, and beyond, making a significant impact in the world of technology.

We offer creative and flexible solutions to ensure the quality of your business operations, safeguarding your brand's reputation. We're proud to say we've been pushing the boundaries for over 25 years now, always striving for innovation and delivering exceptional service.

Ready to make a difference? Join our dynamic and forward-thinking team!

 

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.

 

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
  • Excellent personal skills, successfully collaborating in cross-functional environment

 

Why should you join us?

 

  • Recognized among Israel's top 100 best places to work for, four years in a row
  • Be part of a company that is a globally recognized leader in Quality Engineering
  • Experience our team spirit, working with real people, and solving real challenges
  • Work with Senior Specialists and Practice Experts. · Nurture your personal and professional growth through tailored career paths
  • Dive into interesting projects using cutting-edge technology designed by and for Quality Engineers
  • Enjoy unique placement opportunities worldwide
  • We believe in a workplace culture that values open communication and fairness, encouraging our employees to feel seen, supported, and empowered to realize their full potential

 

 

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