Regulatory Affairs GPH Expert at Johnson & Johnson
Employment Nigeria
04-Aug-2023
₦Not Available
LAGOS ,
Public Relations
At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s largest and most broadly based healthcare company, we are committed to using our reach and size for good. We strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.
Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to profoundly change the trajectory of health for humanity.
We are recruiting to fill the position below:
Job Title: Regulatory Affairs GPH Expert
Job ID: 2306121340W
Location: Lagos, Nigeria
Job type & Duration: Contract (1-year)
Job Description
- We are currently recruiting for a Regulatory Affairs Expert for their GPH RA team. In this role, you will develop and lead GPH Regulatory Affairs activities, strategy, operations, and compliance activities in African countries' Markets. This is a contract of one year.
- You will act as a Regulatory Cluster Value Team (RA CVT) member and as an Expert for the corresponding portfolio for small molecules.
- You will also be responsible as liaison and main contact between the Local Operating Companies and our international teams such as the Therapeutic Areas teams, CMC teams, Labelling teams, and Regulatory Quality teams.
- Next to this, you will provide regulatory support for tenders and support daily business and product supply in accordance with J&J guidelines and local laws & regulations as well as ensure optimal compliance to local, regional, and Janssen regulations, to minimize risk for the patient and Janssen business.
Core Duties and Responsibilities
Act as Regulatory Cluster Value team (RA CVT) member and as RA Expert for the corresponding Portfolio of Small molecules:
- Provide strategic and valuable RA input into CVT and Value excellence teams.
- Act as regulatory representative on project teams and provide advice on specific projects contributing to developing project plans and target product profiles.
Ensure new products registration:
- Execute regulatory plans and manage timelines to achieve the stated goals.
- Coordinate the preparation, review, submission, and follow‐up of regulatory files that are accurately formatted and follow local regulations in the markets.
- Track and follow up with local marketing authorization holder/distributor submission of regulatory files (including but not limited to variations and responses to questions) to local Health Authorities and ensure that filing and submission meet local requirements and company objectives.
Maintenance and follow‐up of marketed products:
- Coordinate all vital aspects of the product's life cycle management in compliance with local regulations and internal procedures.
- Distribute/share official notifications and HA information with internal customers as applicable.
- Ensure close follow-up with partners to ensure timely submission and reporting
Liaison and main contact between LOC and international & external collaborators:
- Keep EMRL informed of regulatory status in LOCs and forward their requests and relevant information from LOCs.
- Keep a timely and transparent communication flow of critical priorities and decisions. And keep alignment across different stakeholders in a timely manner.
- Key external participation in Industry groups with a structured approach to sharing within internal teams
- Supervise the team and ensure alignment on strategy and timelines commitments
Maintain archiving and appropriate databases and systems:
- Ensure electronic and paper tracking of regulatory activities Marketing authorizations and lifecycle management via appropriate systems
- Populate and update appropriate J&J databases as per J&J processes.
- Update, maintain, and use regulatory databases, tracking tables, and information systems.
Compliance Responsibilities:
- Ensure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOPs (Standard Operating Procedures), are met and, where applicable, appropriately managed.
- Ensure HCC and legal requirements (Fair Market Value, Transfer of Value rules, Promotional Materials rules) are fully understood, appropriately managed and, where applicable, complied with when planning projects, developing materials, executing projects, and contracting vendors
Daily business & product supply Support:
- Support Ad Hoc requests and ensure interactions with Heath authorities
- Provide regulatory support to all company functions upon request.
Other features of the job:
- Keeps overview of all TA-specific activities:
- Monitoring implementation of procedures
Candidate Profile
Educational qualifications:
- Minimum of a Bachelor's Degree in Scientific / pharmacist with initial experience in Regulatory Affairs. Ideally, you have a Master's Degree within the scope of Regulatory Affairs.
Knowledge & Abilities:
- Good knowledge of regulatory requirements, local Health Authority regulations & guidelines, as well as regulations from other countries.
- Good level of English
- Knowledge, understanding, and interpretation of legislation
Skills:
- Excellent communication and presentation skills, both verbal and written
- Ability to manage multiple assignments
- Awareness and ability to understand the broader picture of compliance and launch time
- Strong interpersonal skills to deal with sensitive and occasionally contentious issues.
How to Apply
Interested and qualified candidates should:
Click here to apply online
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