In this role as a Regulatory Affairs Officer, you will be responsible for building regulatory strategy, determining applicable regulatory requirements, proposing solutions to comply with regulatory requirements, and managing product license registration with the appropriate regulatory authorities worldwide.
An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Department.
As the Regulatory Affairs Specialist you will be responsible for maintaining the integrity and compliance of medicinal product imports, ensuring the highest standards are met in line with industry regulations.
We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area.
This will be a hybrid role consisting of 3 days on site and 2 days working from home.
We are seeking a talented Regulatory Affairs Specialist to join our client's regulatory team in support of the expansion of their ISO 13485 diagnostics product pipeline.
Reporting to the Regulatory Affairs Manager, you will play a crucial role in ensuring regulatory compliance and supporting the successful submission of our products to global regulatory agencies.
As Regulatory Affairs Specialist responsibilities include
Collaborate closely with the Regulatory Affairs Manager to develop and maintain technical files and submissions for global regulators.
We are seeking a Quality Assurance / Regulatory Affairs Officer to support this global medical device company in meeting its quality and regulatory requirements.
Provide technical support for medical device manufacturing, engineering, and distribution.
Evolve are recruiting for a leading medical technology organisation who are seeking a Quality Assurance and Regulatory Affairs Officer!
You will be responsible for providing technical support, guidance, and discipline for medical device manufacturing, and distribution in quality assurance, regulatory compliance, and quality systems.
This role is based in Essex and is a full-time permanent position, however hybrid/remote working is available for up to 2 days per week.
Do you have quality assurance and regulatory affairs experience within the medical devices sector?
An excellent role on offer for an individual with quality assurance and regulatory experience within the medical sector looking to play a key role at an industry leading company.
Would you like to work for a world leading company?