Job description

Description

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 jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

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About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Regulatory Affairs Professional - KSA & Gulf. This hybrid work position will be located in Cairo, Egypt.

Essential Job Duties and Responsibilities:

• Execute regulatory plans and manage timelines to achieve the stated goals.

  
  
  

• Coordinate the preparation, review, submission, Tracking and follow-up of regulatory files (including but not limited to: New MA dossiers, renewals, variations, response to questions) that are properly formatted and in compliance with local regulations. Prepare local/administrative sections where no local regulatory responsible is designated according to country specific requirements.

  
  
  

• Act as liaison and main contact between LOCs and international groups: I. Receive, assess completeness/relevance, track and archive core dossiers received from international groups. II. Forward all relevant information/data from and in accordance with international group LOCs. III. Keep international groups informed of regulatory statuses in LOCs and forward to them requests and relevant information from LOCs.

  
  
  

• Maintain archiving and appropriate databases and systems: I. Ensure electronic and paper tracking of regulatory activities and Marketing authorizations lifecycle. II. Ensure archiving of regulatory dossiers. III. Populate and update appropriate J&J databases as per J&J processes. IV. Update, maintain and use regulatory databases, tracking tables and information systems.

  
  
  

Daily business & product supply Support:

• Provide guidance to peers within J&J and other external partners.

  
  
  

• Assess the registration status for the manufacturing sites for assigned products across GCC

  
  
  

• Support in planned life cycle management for assigned products across GCC d. Update our systems and tools to leverage digital

  
  
  

• Comply with local laws & GCC guidelines

  
  
  

• Communicate with GCC disturbers to assess products and sites registration and renewal status to allocate requirements

  
  
  

• Communicate with internal stakeholders to provide all the local requirements for regulatory activities.

  
  
  

Compliance Responsibilities:

• Ensure safety reporting requirements as set out in company policies and SOPs (Standard Operating Procedures) are met and, where applicable, appropriately managed when planning projects, developing materials, executing projects, and contracting vendors

  
  
  

• Ensure inspection readiness with respect to personal training compliance, and availability of recent CV and individualized Job Description

  
  
  

Special requirements:

knowledge of GCC regulations is desirable

Job Requirements

• Pharmacist or Scientific Degree

  
  
  

• 3 years’ experience in Regulatory Affairs with Regional Responsibility

  
  
  

• Good knowledge of regulatory requirements, HA regulations & guidelines in GCC Countries

  
  
  

• Good communication and presentation skills, both verbal and written

  
  
  

• Demonstrated ability to manage multiple assignments

  
  
  

• Anticipation and planning skills

  
  
  

• Highly organized

  
  
  

• Ability to work cross-functionally

  
  
  

• Desire to work as part of an effective, cohesive group

  
  
  

• Good level in English and Arabic languages.

  
  
  

Other requirements

Skilled in Outlook and Microsoft office applications

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