Regulatory Affairs is an essential function within the pharmaceutical and healthcare industries. The role of the Regulatory Affairs function is to ensure that all developed products are safe and effective for use. The term “products” in this sense encompasses a wide range of commodities which include pharmaceuticals, medical devices, cosmetics and chemicals/biocides.
A Regulatory Affairs role will vary depending on the level of seniority. However, a few examples of what a role within this sector could entail are set out below:
Typical roles within the Regulatory Affairs sector are:
If you are looking to progress your career within Regulatory Affairs you will need to have excellent communication skills, a keen interest in learning and great attention to detail in your work.
In addition to these characteristics, there are several extra duties you can undertake to help advance your career:
There are several obstacles candidates may need to overcome to enter the industry:
If you are looking to transition into a role within Regulatory Affairs, it is highly recommended that you have experience within a related industry i.e. quality assurance, quality control, compliance etc. This enables candidates to gather practical experience in drug development and gain a better understanding of all associated processes involved.
Typical career progression opportunities within Regulatory Affairs could look like:
A career within Regulatory Affairs can be a rewarding one. In addition, if you’re passionate about science and drug development you’ll gain a lot of exposure and insight into the full lifecycle of the products. If you possess these key attributes mentioned previously and are passionate about the industry, a career within this versatile sector may be ideal for you. Visit our jobs page to browse our live vacancies.