About this role
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Your Role: As a Quality Validation Expert, you will be responsible for identifying, planning, and implementing validation requirements in a cGMP environment. This includes overseeing cleanroom, equipment, instruments, and manufacturing/testing processes in a Green Field Pharma facility. You will prepare and execute IQ/OQ/PQ protocols, coordinate computer system validation, and ensure compliance with applicable standards.
Who You Are:
Minimum Requirements:
- Master of Science (Life Science) from a reputed institution or B.Tech or Engineering background.
- Minimum of 8 years of experience, with at least 5 years in quality assurance within reputed pharmaceutical industries or research institutes.
Maximum Requirements:
- Develop and maintain the validation master plan (VMP).
- Conduct risk assessments and ensure compliance with cGMP, GAMP 5, and FDA regulations.Collaborate with Quality, Production, Engineering, and IT teams to drive validation and quality assurance deliverables.
- Participate in internal and external audits and respond to findings related to validation.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Other facts
About The businesses of Merck KGaA, Darmstadt, Germany
We are Merck KGaA, Darmstadt, Germany and its global affiliates. We are a leading global science and technology company headquartered in Germany.
We are curious explorers, courageous pioneers, and ingenious inventors. Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Life Science, Healthcare, and Electronics.
Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and the planet.
We believe in the positive power of science and technology. It has determined our actions since 1668 and inspires us to continue researching for a future worth living. As a family-owned company with over 350 years of experience, we stand for sustainability, responsibility, and innovative strength.
We take pride in being a diverse and inclusive company that values and fosters the talents and abilities of our employees. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Privacy Statement: https://www.emdgroup.com/en/privacy-statement.html
What you'll do
- As a Quality Validation Expert, you will identify, plan, and implement validation requirements in a cGMP environment. This includes overseeing cleanroom, equipment, instruments, and manufacturing/testing processes.
Ready to join The businesses of Merck KGaA, Darmstadt, Germany?
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