Állás részletei
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Cég neve
Cognizant
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Munkavégzés helye
Hibrid • Mill Park - Budapest, Épület, MillPark Centre, Soroksári út 44 A-2nd Floor, 1095 -
Fizetés
Bónusz -
Egyéb juttatások
- Szakmai tréningek
- Nyelvtanulás támogatása
- Sport támogatás
- Élet- és balesetbiztosítás
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Munkaidő, foglalkoztatás jellege
- Teljes munkaidő
- Alkalmazotti jogviszony
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Elvárások
- Angol felsőfok
- 1-3 év tapasztalat
- Egyetem
Állás leírása
About us
Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2025) is consistently listed among the most admired companies in the world.
Responsibilities:
The position exists to participate in the regulatory program of our pharmaceutical partner, being part of a global team and leading a team which is part of it.
- 40 hours per week
- Normal business hours
- Office attendance: Once a week
Tasks and Responsibilities
- Tracking different regulatory submissions in the corporate regulatory database – update database with specific documents and/or information
- Running daily queries, providing reports to client stakeholders
- Applying technical knowledge to perform quality check on the entries
- Ensuring compliance with KPIs
- Optimizing utilization and effective resource allocation planning for the team
- 100% compliance for work allocation
- Good team management (indicated through no major escalations)
- Ensure adherence to Cognizant and Client SOPs (Standard Operating Procedure) or internal standards and processes
- Responsible for regular FMEA update and CAPA management
- Managing BCP and operations
- Effective risk management and issue handling by conducting daily huddle and escalating them on time
- Communicating with client representative, understanding client expectations
- Establishing and developing processes and procedures in the team
- Complete all mandatory training courses as applicable
- Communicating issues to Delivery Site Lead
Your profile:
- Education: Bachelor’s degree in Life Sciences or Pharmacy
- Experience:
- 2–5 years of professional experience in Regulatory Affairs
- Hands-on experience in Pharmacovigilance (PV) data handling
- Skills:
- Strong attention to detail and accuracy in documentation
- Good understanding of regulatory guidelines and compliance standards
- Proficiency in data management tools and MS Office applications
- Language: Excellent written and spoken English (additional languages are a plus)
We offer:
- Competitive salary and cafeteria benefits; All You Can Move SportPass (at a discounted price), annual bonus, medical benefits, and other perks
- Risk and accident insurance
- Chance to be part of a rapidly expanding organization
- Training and continuous learning and certification opportunities
- Multilingual environment, native colleagues
- Pleasant and inspiring working atmosphere with multicultural community and state-of-the-art technologies
- Easy-to-access location and modern office building (easy to reach from city center, 10–15 minute commute)
- Reimbursable language courses
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