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Regulatory Affairs Executive / Regulatory Affairs Associate at GlaxoSmithKline (GSK)


GlaxoSmithKline (GSK) is a science-led global healthcare company with a special purpose to improve the quality of human life by helping people do more, feel better, live longer. Every day, we help improve the health of millions of people around the world by discovering, developing and manufacturing innovative medicines, vaccines and consumer healthcare products.

We are building a stronger purpose and performance culture underpinned by our values and expectations - so that together we can deliver extraordinary impact for patients and consumers and make GSK a brilliant place to work.

We are recruiting to fill the position below:

 

Job Title: Regulatory Affairs Executive / Regulatory Affairs Associate

Requisition ID: 348642
Location: Ilupeju, Lagos
Employment Type: Full-time
Categories: Regulatory

Job Purpose

  • As a Regulatory Affairs Executive you will ensure products within scope can be placed on the market with optimal yet compliant claims, advertising, and promotion in line with commercial plans.
  • You will ensure products are maintained and meet internal and external compliance requirements.
  • You will also be a productive part of defined Cx local regulatory team, including being a proactive partner to other stakeholders, e.g., marketing/sales within local commercial business, supply chain (GMS) and quality etc.

Essential Job Responsibilities:

  • Manage preparation of regulatory documents, dossiers and applications to enable new products to be launched and maintained in market, with the correct alignment and compliance to regulations, proactively seeking innovative and rapid path to market.
  • Manage compliance within defined portfolio/activity streams in line with GSK CH expectations -  support key processes and ways of working (e.g., in relation to GSK CMC, quality, product labeling requirements as well as local MoH regulations).
  • Work together with other functions (e.g., marketing, supply chain) to deliver NPD and value engineering projects.
  • Support the development of the strongest claims/advertising and promotion possible within the regulations, ensuring risks are appropriately addressed and communicated.
  • Analyse regulatory issues and communicate with key stakeholders. Work together to help develop plans to mitigate, so that we can deliver science that is robust and aligned with business needs.
  • Actively contribute to the activity of a high performing local teams, including looking for ways to improve the performance.
  • Build relationships with key stakeholders and represent GSK in an appropriate manner according to company values, in order to present GSK CH policies and strategies.

Basic Qualifications
Why you?

  • BPharm or BSc Degree
  • Relevant 2 year’s experience in Regulatory Affairs.

Preferred Qualifications:

  • Regulatory clearance is a pre-requisite of any product marketing
  • Compliance to regulatory requirements and management of health authorities is essential to Corporate compliance
  • Ability to effectively communicate and negotiate in relation to technical information and regulations is key.

 

How to Apply
Interested and qualified candidates should:
Click here to apply


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