Qualitest is the world’s leading AI-Powered Quality Engineering Company.
We bring in the culture of quality orchestration, technology, and operational landscape through our engineering-led, process discipline.
We provide innovative and scalable business quality engineering solutions that protect our client’s brand through end-to-end value demonstration with a laser focus on customer experience and release velocity. This year we are celebrating 25 years of innovation and excellence.
Every day with Qualitest is an opportunity to innovate, grow and change.
We’ve assembled one of the largest, most talented groups of creative, critical problem-solvers in the world with over 7000 engineers.
Talented, intelligent, and passionate people have made Qualitest the world’s leading Quality Engineering company. If you want to learn from the best, there’s no better place to start!
We’re seeking a Validation Specialist for an exciting and challenging position!
Ready to advance your career, team up with global thought leaders across industries, and make a difference every day? Join us at Qualitest!
This is a full-time, on-site position located in Rehovot
Responsibilitie:
- Develop and execute cleaning validation/verification protocols for all commercial and R&D manufacturing, processing, and food equipment.
- Perform proper and timely sampling of in-process/intermediate products and finished products as outlined by validation/qualification protocols.
- Gather photocopies and compile relevant documentation such as executed batch records, certificates of analysis and equipment logs.
- Investigate and resolve deviations/exceptions from the predefined acceptance criteria.
- Write and review validation/qualification protocols and reports for facility, utility and production equipment .
- Interact and coordinate compliance efforts with other departments including Operations, Engineering, QA, laboratories (QC and R&D).
Requirements
- BS.c degree in Chemistry, Pharmacy, Engineering or related Science.
- At least 5 years of proven experience in pharmaceutical or other highly regulated industry.
- Knowledge in bioprocess equipment and their relent parameters.
- Knowledge of regulated biotechnology or drug validation requirements.
- Knowledge of manufacturing processes, sampling techniques, government regulations and guidelines pertaining to those areas.
- Strong understanding of cGMPs and validation/qualification concepts.
- Excellent written and verbal communication skills in English.
Benefits
Why Qualitest?
- Have continuous access to and work with Senior Specialists and Practice Experts
- Be a part of a leading company, globally recognized as a Visionary by Gartner Magic Quadrant
- As a global company, we offer unique placement opportunities around the world
- Never stop experimenting and learning with Qualitest Tech academy: training courses, mentorship programs, technical tribes, sponsored certifications, leadership programs, and much more
Intrigued to find more about us?
- Visit our website at www.qualitestgroup.com
- Check out our Career page:https://qualitestgroup.com/careers/open-positions/
If you like what you have read, send us your resume, and let’s start talking!
