Job Vacancy at Lorache Consulting

Job Role

• Candidates will work for research organisations, medical, pharmaceutical, chemicals and other alternative medicines manufacturers to ensure that what their company produces complies with registration.
• Regulatory affairs officers ensure manufactured products are appropriately licensed, produced and marketed.
• Regulatory officer will negotiate between the company they work for and the appropriate regulatory body to ensure that their product meets all the necessary regulations
• Regulatory affairs officers ensure the appropriate licensing, marketing and legal compliance of pharmaceutical and medical products, in order to control the safety and efficacy of products
• Ensuring that a company's products comply with the regulations of the Medicines and Healthcare products Regulatory Agency (MHRA).
• Keeping up to date with international legislation, guidelines and customer practices in all countries that the company is exporting to.
• Collecting, collating and evaluating scientific data that has been researched by colleagues;
• Undertaking and managing regulatory inspections and reviewing company practices and providing advice on changes to systems;

What to Expect:

• This is a desk-based role, involving the close study of scientific and legal documents. It also requires close working with scientific and medical personnel, often on a project-team basis.
• Regulatory affairs roles have considerably broadened in scope within the last few years and usually entail involvement throughout the lifecycle of a product.
• Work in larger companies is often in their regulatory affairs departments, while smaller companies may employ only one or two specialist staff.

Qualifications

• B.Sc in any discipline with 3 years hands on experience from a similar organisation