Regulatory Affairs Professional
Há 4 horas
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at
Job Function:
Regulatory Affairs GroupJob Sub Function:
Regulatory AffairsJob Category:
ProfessionalAll Job Posting Locations:
Porto Salvo, PortugalJob Description:
Job Description
REQUIRED EDUCATION & EXPERIENCE
Special Requirements
Fluency in the national language(s) and the English language required.
General knowledge in life sciences, scientific acumen and communication skills.
Basic understanding of the APIFARMA's Code of Practice.
Basic understanding of pharmaceutical product development
Product RA legislation knowledge, understanding and interpretation
General understanding of business partners needs
ESSENTIAL KNOWLEDGE & SKILLS
Good communication and personal relationships skills.
Leadership and motivation capabilities for specific projects. Able to gather and transmit information in a clear and simple way.
Teamwork mind orientation.
Organized and accurate in the execution of all tasks individually.
Persistent, dynamic, creative, looking for opportunities and flexible.
Able to use new technologies like the Internet as a valuable tool on his/her work, Knowledge of relevant IT-systems
Able to manage multiple projects, priorities, and complex systems simultaneously
Able to work under strict timelines, combined with flexibility when emergency situations require this
Project management skills
Required Skills:
Preferred Skills:
Analytical Reasoning, Business Behavior, Business Writing, Collaborating, Communication, Confidentiality, Data Reporting, Data Savvy, Detail-Oriented, Execution Focus, Legal Support, Medicines and Device Development and Regulation, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments-
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