A specialist, international Pharmaceutical company is actively seeking a Regulatory Affairs Manager due to their successful company growth and dedication to innovate new products.
The role reports directly to the Head of Regulatory Affairs and is responsible for pre-approval regulatory activities that support the delivery of the company's strategic plans.
This is an excellent opportunity to work across a number of product ranges in a growing company that is expanding globally with a focus on delivering medicines to the paediatric market.
SRG are currently looking for a Regulatory Affairs Associate for a Global Healthcare Company who have opened a new vacancy within their Regulatory team on an initial 6-month basis based out of their offices in Tadworth.
The role enables market access for products regulated as Food Contact Materials in the UK & EU and General products in the UK & EU and requires knowledge of the current National Food Contact materials and General Product regulations in order to conduct regulatory assessments and ensure compliance as well as to develop processes to sustain compliance.
Senior Manager - Regulatory Affairs EU Oncology, remote working
This well-known biotech is looking for an experienced Senior Regulatory Affairs Manager to join an established Regulatory Affairs team on a fully remote basis.
Regulatory Affairs Labelling Manager; Your new company
This consultancy is looking to strengthen their Regulatory Labelling group by taking on an experienced Regulatory Affairs Labelling professional for a contract job.
This job is outside IR35 and has scope for extension.
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved.
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract.
Other responsibilities include
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.