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Senior RQS Data Specialist (all genders) - job post

Merck Group
3.8 na 5 gwiazdek
Warszawa, mazowieckieHybrydowo
Pełny etat

Lokalizacja

Warszawa, mazowieckieHybrydowo

Świadczenia

Na podstawie pełnego opisu stanowiska

  • Ubezpieczenie na życie
  • Prywatna opieka medyczna

Pełny opis stanowiska

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.


This role can be done hybrid: 3 days per week from office in Warsaw.

Your Role:

As the Senior Specialist of Regulatory Quality Safety (RQS) Information Management, your primary responsibility is to oversee the management of regulatory and quality data. This includes defining a clear framework for effective information management in regulatory collaborations, establishing standards and principles for data governance, and ensuring the quality of data content to support the organization's strategic goals. You will coordinate people, processes, and technology to create cohesive operational models, define data entry and maintenance rules, and ensure compliance with health authority requirements. Additionally, you will mentor junior team members and oversee external service providers to ensure the effective delivery of tasks.


Who You Are:

  • You possess at least five years of experience in the pharmaceutical or IT industry, with a minimum of three years in regulatory affairs.
  • Your background includes excellent regulatory management and data governance experience, along with a strong command of current regulatory data standards.
  • You are fluent in spoken and written English and have demonstrated experience collaborating with health authorities.
  • Professional with a Master degree in a scientific discipline or equivalent experience in the chemical-pharmaceutical industry especially in the Regulatory Affairs area.
  • Your strong communication skills, attention to detail, and ability to work with uncertainties make you a valuable asset to the organization.


YOUR MAIN BENEFITS:

  • Health and well-being: Get access to private medical care, life insurance, and sports card,
  • Work-Life balance: Enjoy additional paid days off, hybrid working model.
  • Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
  • Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.


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!

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