Regulatory Affairs Professional Porto Salvo

Overview

Join to apply for the Regulatory Affairs Professional role at Johnson & Johnson Innovative Medicine.

Get AI-powered advice on this job and more exclusive features.

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 Med
Tech, 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 https://www.jnj.com

Location

All Job Posting Locations: Porto Salvo, Portugal

Location Details

Porto Salvo, Lisbon, Portugal

Required Education & Experience

• 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 Portuguese Copyright law and how this impacts the Medical Information environment.
• Basic knowledge of literature searching tools and databases, and ability to conduct basic literature searching alone, and complex searches with assistance.
• 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

Seniority level

• Not Applicable

Employment type

• Full-time

Job function

• Legal

Industries

• Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Johnson & Johnson Innovative Medicine by 2x

Get notified about new Regulatory Affairs Specialist jobs in Porto Salvo, Lisbon, Portugal.

Related roles

• Regulatory Affairs Specialist & NIP Deputy
• Regulatory Affairs Specialist - Long term project
• Regulatory Affairs Junior Technician (M/F/D)
• Regulatory Affairs Digital Product Champion (m/f/d)
• Manager RASSU (Regulatory Affairs and Study Start Up) - Global Dedicated Role (EU Region)
• Regulatory Reporting Officer - Large Exposures Sub
  Group
• Credit Risk - Regulatory Reporting Officer
• German Quality Specialist - Lisbon, Portugal
• Business Process Quality – IMS Specialist Professional Portugal
• Product Owner Global Regulatory Affairs (m/f/d)
• Sovereign Cloud Automation Quality Specialist
• Dutch Quality Specialist - Lisbon, Portugal
• Regulatory Affairs Senior Data Steward (m/f/d)
• Sovereign Cloud Senior Quality Specialist
• Sovereign Cloud Senior Quality Specialist

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.