Expiry Date: 07-11-2019
Categories Clinical Research, R & D, Regulatory Affairs
Job Type: Full Time
Location: London, UK
This is a different opportunity to most because the role is focused on managing a small team responsible for ensuring quality for a regulatory function, not a product or normal GxP area. Because of this, I am seeking an individual who has:-
Either way, you will see yourself as someone who can provide solutions into the value chain, by working with different sub teams, different functions and in a role where you will report to the senior management team member (the global RA leadership team), for an individual with a truly remarkable reputation.
You will support cross functional and functional quality programmes, compliance initiatives and manage or maintain oversight for any potential deviations. You will take the SOP landscape with policies through to maturing, as well as through workshops and workstreams, help to map out potential process improvements. You will manage a team of upto 5 FTEs.
The role can be based in 2 locations, 1 is in Benelux, the other is in West London, A4/M4/M25 region. Both come with support for relocation, and both come with a decent package, stock and car or car allowance.
To apply for this role, please register on this web site. My team and I would welcome a phone call in private if you would like to explore this role and opportunity, then please contact either myself, Theo Moore, or my colleague Matt Greig, in the London office on +44 (0)20 7801 3384, or at any time during evenings on +44 (0)7918679405.
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Keywords / Key words: Quality Management, Regulatory Processes, Training and Standards, Regulatory, Process Improvement, Jobs in Regulatory & Compliance, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs.