GSC's vision is to be a patient-centric, integrated supply chain, launching and supplying innovative products that deliver hope to patients through life-changing medicines.
Global Clinical Supply Chain (CSC) is a new organization within Global Supply Chain (GSC).
Contract Duration: 12 Months Flex to be extended/perm
Our patients are at the heart of everything we do, and we're proud to offer legendary care every day; it's what sets us apart from other UK Pharmacy chains.This is a great opportunity to develop your Pharmacy career and make a difference to the lives of our patients.
Be part of our ambition to be the world's leading Pharmacy-led retailer.
Our client, a global pharmaceutical company with innovative and exciting growth plan, they are currently looking for a Buyer to be part of their team (indirect spend categories).
You will be an expert negotiator with confidence working through supplier contracts with consistent awareness of balancing cost, quality and time.
Primarily focusing on the UK operation, additional support will be given to Germany as part of the role.
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.
Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Manager to join their team in Uxbridge on a full time, 12-month temporary basis (35 hours per week).
This role is expected to be worked on a hybrid basis but remote applications will also be considered.
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.
General
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract.
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.
Posted by Hays Specialist Recruitment Limited • £50/hr to £58/hr
Global Biotechnology in the UK are looking for a Regulatory Affairs Manager to develop and implement regulatory strategies for EU markets for their Oncology portfolio.
This position will sit within the global regulatory team and will require someone to have both development and post-marketing experience.
Our client, a global pharmaceutical company is currently looking for a Senior Regulatory Affairs Portfolio Manager to join their team based on the outskirts of London on a full time, 8-month temporary basis (35 hours per week).
This opportunity will see you working with senior stakeholders to develop, execute and deliver the regulatory strategy for assigned products.
This is a remote-by-design role which will require flexibility to attend key meetings on-site (Uxbridge).
Posted by GPD Healthcare Limited T/A ThinkWorkForce • £75/hr to £80/hr
Department: Urgent Care
Our client operates an award-winning Urgent Treatment Centre (UTC) designed to provide exceptional care for patients with minor injuries and illnesses.
The UTC supports the Emergency Department (ED), allowing the ED to focus on life-threatening conditions.
The role involves liaising with laboratories on regulatory submissions, communicating with suppliers and staff members of all levels, and educating / guiding personnel and customers about compliance regulations
The postholder will be responsible for making sure company products meet regulatory and safety standards of relevant countries.
Certification Engineer (FTC until end of June 2025) required by a leading global engineering company based in West London.