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Job Details

Director Regulatory Affairs – global pharma company – Munich – up to 130,000 € plus bonus

Company: Meet
Location:
Reference: DirectorRAoncology
Closing Date: 29 Dec 16
Type: Full Time
Salary (£): 100,000+
Benefits:

Job Summary:

We are looking for an experienced Senior Regulatory Affairs Manager who wants to use his knowledge about strategy development in a global researching pharmaceutical organization in Munich. You can expect an open environment, life-changing projects and excellent benefits.

Requirements:

Company background

 

We are one of the top pharmaceutical companies worldwide with over 100 year of experience and a strong focus on research and development of new life-saving drugs in variety of indications. Currently we have several exciting new projects in the pipeline and therefor need a senior specialist to join our global regulatory team in Munich,

If this sounds appealing to you, please contact Aine Uusvel from Meet via email aine@peoplewithchemistry.com or via phone +44 789 650 6004. The applications will be handled with discretion.

 

Job description

 

As Director Regulatory Affairs you will have the following responsibilities:

 

·         Responsible for the development, implementation, and communication of the regulatory strategies

·         Planning and managing regulatory documents and submissions during development and life cycle management 

·         Participating in critical development projects from full development up to registration and the early post-authorization phase

·         Acting tas regulatory contact person for authorities, external partners and in-house functions

·         Maintaining approvals of applications for Clinical Trials and Marketing Authorizations for assigned products.

·         Develop structure for high-level dossier  and align with senior management and key stakeholders on dossier content

 

Qualifications

 

Ideally we are looking for candidates with the following qualifications:

·         Degree in a Life Science or related discipline

·         Minimum of 8 years’ experience within regulatory affairs in EU or global 

·         Experience in preparation and management of successful CTA/MAA submissions

·         Oncology experience is a must

·         Ability to lead and motivate cross functional teams

·         Fluent in English, German language is not required

 

Full job description and company details are available upon application, apply below. This position is being dealt by Aine Uusvel at Meet, please call on +44 203 019 5973. You can also e-mail us directly at aine@peoplewithchemistry.com to discuss in confidence.

Meet are good people who are great at recruitment. We’re proud to partner with the industries leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available.  We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way.

Key words: Senior Regulatory Affairs, Regulatory Affairs Manager, European Regulatory Affairs, Reg Affairs, Associate Director, Director, Director Regulatory Affairs, AD, Associate Director Regulatory Affairs, IND, Clinical development, global strategy, strategy development, regulatory strategy, Ausbrug, Munich

 

 

Apply for this job: Director Regulatory Affairs – global pharma company – Munich – up to 130,000 € plus bonus

Contact Information:

Address:  meet
Euston Tower Levels 32-34 286 Euston Road London
NW1 3DP
England
Tel:  +44 203 178 7488
Website:  Visit Our Web Site

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