Regulatory Affairs Placement

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Regulatory Affairs Placement

Degree Requirements

Must be on track for a 2.1 (or above) in an undergraduate degree in life science, pharmacy or equivalent discipline appropriate for the role.

You will have completed a minimum of 2 years of an undergraduate degree, but will not have graduated at the start of your placement.

Detailed description and scope of the role:

Business Skills & Competencies

• Degree in pharmacy, chemistry or life science
• Ability to work under limited supervision and prioritise work load accordingly
• Demonstrate ability to show attention to detail
• Good customer focus and team player who has the ability to work with a large group of people
• Strong interpersonal and written communication skills with the ability to communicate effectively across business functions.
• Strong IT skills and ability to work with a variety of systems

Job Purpose

• To help ensure that existing UK Product Licences are maintained and new Marketing Authorisations are obtained to allow continued and future sale of categories of Consumer Healthcare products in the UK.
• To help ensure that all regulatory activity for a specified portfolio of products is planned and geared to commercial requirements.
• To help ensure that all cosmetic products are sold in compliance with the Cosmetics Directive, that all medical devices are sold in compliance with the Medical Device Directives and that all pack and promotional copy complies with regulations and Codes of Practice.

Key Responsibilities:

• To have responsibility with the support of a Regulatory Category Manager for projects involving marketed and development products and to be responsible for progressing the regulatory status of these products in the UK in such a manner as not to interfere with the marketing and the development activities of the business.
• To have a general understanding of the regulatory environment.
• To prepare submissions which are both accurate and high quality and ensure all files and databases are effectively managed.
• To maintain relationships with regulatory authorities to expedite smooth and timely assessment of all applications.
• To be responsible with the support of a Regulatory Category Manager for advising marketing and Global Manufacturing and Supply on the regulatory implications of technical changes
• To develop knowledge of the regulations and guidelines and working practices of the EC and UK Regulatory Authority.
• To develop some knowledge of the Cosmetics Directive and PIPs, and Medical Devices Directive if relevant to the category.

Requires:

• Ability to prioritise work load
• Demonstrate ability to show attention to detail
• Good customer focus and team player who has the ability to work with people from a large range of disciplines.

Additional Details:

PLEASE NOTE: The Assessment Centre date for successful applicants is expected to be in December 2018.

If you have what we’re looking for apply today!

We recruit on an on-going basis and prioritise applications based on the application date.

We will close for applications when we have filled our assessment centre dates.

This opportunity has the following recruitment stages you must successfully pass to be offered a placement year with GSK for 2019!

• Eligibility Form
• Online Assessment
• Application Form
• Assessment Centre

About GSK

One of the world’s leading healthcare companies, GSK discovers, develops, manufactures and distributes life-saving vaccines, prescription medicines and consumer health products such as Maxinutrition, Sensodyne, Aquafresh and Panadol.

The size and scope of our organisation allows our people to answer some of the biggest questions facing everyone on the planet – questions about future healthcare needs and questions about building a responsive, innovative, global business to meet them – as well as questions about their own personal and professional growth.

How to apply

To apply for this role and to find out more, please click on the apply button.