QA Validation Specialist

3 settimane fa

Modugno, Italia Merck Group A tempo pieno

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.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your Role:

As QA Validation Specialist you will be the quality reference in the management of site Computerized Systems, oversighting validation activities around equipment and CS to ensure compliance with GMP, FDA, EMA, and other regulations. You will support Operations and Technical Services with root cause investigation of deviations and nonconformities concerning validation and risk assessments and implementation of mitigation strategies. Moreover, you will be responsible to encourage a continuous improvement culture; provide expertise in the review of validation protocols, reports and investigations carried out during processing problems and deviations. You will also support the definition and monitoring of Key Performance Indicators and dashboards to help measure progress, in terms of cycle time and compliance-related metrics.

Who you are:

  • Scientific degree (e.g., Pharmacy, Biology or Chemistry)
  • 1-3 years’ experience in the pharmaceutical industry with a particular knowledge in QA and CSV
  • Profound customer-orientation with an eye for the company’s own interests
  • Flexibility and keen pursuit of innovation throughout all processes in the continuous search of sustainable new ideas
  • Strong desire to develop and grow by way of taking responsibility and engaging in additional tasks and operations.
  • Fluent in Italian and English

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team

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