Project Manager Global Regulatory CMC Lead (code CH 170120)

Reference: MI10497F

Expiry Date: 30-06-2021

Category Regulatory Affairs

Salary: Competitive

Job Type: Full Time


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Job Description

Project Manager Global Regulatory CMC Lead

Note: My client has committed to do digital hiring using Skype (VC), and has a new digital on-boarding and induction training process in place to allow a smooth transition during MERS-COV-2 outbreak. During the next period, new hires will be allowed to work from home full-time, until such a time occurs when normal working returns.

About My Client

What I like about this company, is they have continually expanded in the last 15 years, and have achieved several high profile approvals, in disease areas where there was literally nothing of note previously to prescribe, and have delivered this expansion with a keen eye on quality and compliance. This role delivers as the business process owner with oversight for the Quality environment for regulatory and CMC.

This role is offered at Senior Manager grade which would equalize to other companies as somewhere between Senior Manager and Associate Director in terms of basic salary. The company offer Senior Managers a decent stock plan, which is unusual in the pharma industry and when you realize who my client is, you will understand the value of this employee benefit.

The Role

You will initiate, co-/lead with the partners / co-/sponsors, programs and workstreams aimed at producing more effective systems and processes, for a company which has 4 main technical workstreams, all with differing pharmaceutical development pathways, and for a worldwide supply chain which encompasses over 100 plus countries.

You will be regulatory aware, but this could be from doing a process improvement role in manufacturing and supply chain, or quality assurance, or pharma development, as well as within regulatory itself – my client is satisfied with any of these paths to this type of role. Also, if you have worked in a regulatory operations group, and have strong project management, then you would also be applicable.

You will ideally have any structured methodology for project management as well as 3 plus years’ experience in leading ideally regional or multi-national, business process improvement programs within a pharmaceutical or a biotechnology company.

Package & Benefits

This role comes with a decent package including a high performing stock plan, bonus and normal Swiss benefits.

To Apply!

To apply for this role, please press the red “Apply for position”, or contact Matt on +44 (0)20 7801 3386. We wish you a successful 2020 and fortuitous year! 

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