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GET STAFFED ONLINE RECRUITMENT LIMITED is recruiting a Regulatory Affairs Officer for a 12-month FTC based at the Innovation Centre in Bedford with hybrid working options. The role involves administrative tasks and preparation of regulatory documents to support regulatory initiatives and device registrations.
Ideal candidates will be highly literate and numerate with excellent written and oral communication, capable of engaging with stakeholders and representing the company professionally.
Salary: £25,000 – £31,000 /annum DOE plus benefits
Location: Bedford
Full-Time, Fixed-Term for 12 months
Our client is a world leader in the research, design and supply of advanced consumer diagnostic products. They are a joint venture, and their brand is recognised the world over as providing accurate home pregnancy and fertility monitoring tests.
They are looking for a Regulatory Affairs Officer to join their Regulatory Affairs team on a Full-Time, Fixed-Term for 12 months basis.
The role will be based at their Innovation Centre in Bedford, UK with option for Hybrid Working.
This is an excellent opportunity for someone looking to take their first steps into working within a Regulatory Affairs department. The role will include both administrative tasks as well as preparation of documents to support regulatory initiatives within the department. The role will also help with device registration activities and track regulatory surveillance tasks.
Our client is looking for someone who is highly literate and numerate with a keen eye for detail and a passion for accuracy in written work. Applicants will have the ability to engage effectively with a range of stakeholders, both within and outside the organisation, and be able to demonstrate this. The role holder will be expected to represent the company to the highest professional standards so good interpersonal skills and excellent written and oral communication skills are essential.
Previous experience in the handling of sensitive and confidential information is essential along with the understanding of the need for current Quality System / GMP / ISO compliance. Having a high level of IT literacy is essential and the ability to use standard and bespoke software applications would be advantageous.
If you require any reasonable adjustments to support you, at any stage during the application process, just let them know how they can help.
Our client is a world leader in the research, design and marketing of advanced consumer diagnostic products.
Their research centre is at the cutting edge of innovation and is fully engaged in the development of reliable diagnostic products to empower women on their reproductive journey. They are committed to answering the needs of their existing and future consumers, through a continuous flow of new and innovative products.