Role: Technical & Regulatory Coordinator (Graduate)
Location: Hull, United Kingdom
Salary: £22,000 to £24,000
Contract Type: Permanent Full-Time
Candidate: Graduate (no experience necessary)
Rubicon Technical is a technical service provider to the consumer healthcare industry. We work with medicines, medical devices, food supplements, cosmetics, and functional foods, providing expertise in regulatory affairs, medical affairs, development and formulation, clinical nutrition, pharmacology, trade marking, quality management, project management and artwork and pack copy.
Rubicon Technical is a solution driven business. Our skilled team of consultants pride themselves on 'thinking outside the box' and are responsible for providing a range of bespoke technical services to the pharmaceutical, nutraceutical, medical device and cosmetic industries.
Technical & Regulatory Coordinator Role:
This is a fast-paced and incredibly varied role by nature of being a consultancy. The day-to-day requirements of the job will change constantly. Rubicon’s clients range from small, localised businesses to large multinational consumer health companies. This invaluable experience will develop your professional network and give you industry experience that is unrivalled. Your responsibilities would include, but are not limited to, the following:
Regular travel visiting and working with clients all over the UK as well as managing these relationships
Defending and substantiating marketing materials and pack copies from a medical perspective ensuring claims are robust and based in scientific fact
Reporting on formulations and assessing whether they are safe for consumption for different population groups
Managing regulatory affairs projects for medicines, medical devices and food supplements for both the UK and International markets
Writing clinical and non-clinical assessment reports to support the efficacy of certain active ingredients and medicines as well as the effectiveness of medical devices
Assume a role in the set-up, administration and management of quality management systems for food and pharmaceutical manufacturers. This may include transferable skills such as SOP writing and auditing
Attend trade shows and industry meetings in the UK, EU and further afield.
Continual problem solving
Develop service procedures, policies and standards.
Interpret and summarise legislation and guidance documents for various regulatory categories. Application of this knowledge to client work.
Checking artworks and labels for regulatory compliance, providing clear and concise feedback to clients.
Proof reading labels, reports and marketing materials.
The Candidate:
The ideal candidate will have a minimum of a bachelor’s level degree in a biomedical based scientific discipline such as Biomedical Science, Physiology, Pharmacology, Neuroscience, Pharmacy or Human Biology. Other relevant degrees will be considered.
This is a client facing role, with regular opportunity for travel within the UK to visit clients and to Amsterdam where our European office is based. Good networking and social skills are essential. Access to a car for travel is preferred but not essential. Good attention to detail and excellent communication skills are essential.
The Rewards:
Pension
Private healthcare
Employee discount scheme
Flexible working
Death in service
Employer supported volunteering days
Wellbeing days