Proclinical Group in the United Kingdom is seeking a Regulatory Affairs Specialist to shape EU and global regulatory strategies for analgesics and anaesthetics in the pharmaceutical sector. You will manage regulatory submissions (MAAs, CTAs), liaise with EMA and Health Authorities, monitor regulatory developments, and collaborate with EU and Global Leads to mitigate risks and drive lifecycle management.
The role requires a Life Sciences degree and proven regulatory experience in pharma/biotech,
#J-18808-LjbffrGlobal EU Regulatory Affairs Specialist employer: Proclinical Group
Proclinical Group is an excellent employer, offering a dynamic work culture that fosters collaboration and innovation in the field of diagnostic technologies. Employees benefit from comprehensive training programs, opportunities for professional growth, and the chance to make a meaningful impact on customer satisfaction and business success in the vibrant location of Croydon, UK.
