Regulatory Affairs Specialist
Share
Job Location:
Hourly Salary:
Posted on:
Vacancies:
Job Summary
CK Group is recruiting for a Regulatory Affairs Specialist to join a company in the Pharmaceutical industry at their site based in Reading on a contract basis initially for 6 months.
Salary:
63.52 per hour PAYE or 86.22 per hour Umbrella (inside IR35)
Regulatory Affairs Specialist Role:
Our client is the largest and most broadly-based healthcare company. They strive to improve access and affordability create healthier communities and put a healthy mind body and environment within reach of everyone everywhere.
Location:
This role can be remote based in the UK preference for 2 days per week onsite in Reading.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 174 868.
Please note:This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isnt suitable but you are looking for a new role or if you are interested in seeing what opportunities are out there head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Salary:
63.52 per hour PAYE or 86.22 per hour Umbrella (inside IR35)
Regulatory Affairs Specialist Role:
- Ensures the success of new product registrations line extensions and new indications and claims in alignment with the business plan
- Manages the coordination compilation and submission of new drug applications and cosmetics to the regulatory agencies within their geographical and/or brand area of responsibility
- Maintains compliance for all products with local regulations and quality system requirements
- Relevant Bachelors Degree or higher in Life Sciences Chemistry or Pharmacy
- Expertise across a broad spectrum of Regulatory classifications but must have experience in cosmetics
- Oral care experience is preferred but broader cosmetics will also be considered
- Strong knowledge of regulatory strategy and compliance and the ability to apply these to regulatory solutions throughout the product lifecycle.
- Solid understanding of regulatory/medical/safety/quality requirements.
Our client is the largest and most broadly-based healthcare company. They strive to improve access and affordability create healthier communities and put a healthy mind body and environment within reach of everyone everywhere.
Location:
This role can be remote based in the UK preference for 2 days per week onsite in Reading.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 174 868.
Please note:This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isnt suitable but you are looking for a new role or if you are interested in seeing what opportunities are out there head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Company Industry
Pharmaceuticals
About Company
Idibu
100 employees
Every business is now operating in an environment that’s susceptible to change. idibu has evolved against this changing backdrop. Whether driven by legislation, technology, customer demand or the economy, businesses now need to be agile and fleet of foot to ensure they can attr ... View more
