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Job Details

Regulatory Affairs Associate Director

Company: i-Pharm Consulting
Location: Belgium
Reference: RAD-AN4
Closing Date: 20 Jul 18
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Regulatory Affairs Associate Director, BelgiumAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of products. ...

Requirements:

Regulatory Affairs Associate Director, Belgium

An exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of products.

Job Title: Regulatory Affairs Associate Director
Location: Belgium

Benefits: Above market rate salary + fantastic benefits package

Permanent position

Job Responsibilities:

* To be part of a world-leading, talented and passionate Regulatory team

* Act as regulatory expert in different therapeutic areas for all types of EU regulatory procedures
* Advise other members of the regulatory department and colleagues in other divisions of the company
* Prepare robust strategic responses to address regulatory agency questions
* Contribute to the development of regulatory and business strategies for specified projects or therapeutic areas, as appropriate
* Act as line manager for designated staff, ensuring their operational, training and development needs are addressed appropriately.
* Lead the artwork team to ensure that timing, quality and compliance needs are met for all labelling regulations.
* Take responsibility for the annual regulatory review of discovery and geographical expansion candidates to ensure that investment decisions are optimized.
* Take an active role on the Regulatory Affairs Leadership Team in order to contribute to the strategic direction and financial performance of the department.
* Manage both project and departmental resources, including budget.



Qualifications (education, experience, skills):

* The successful candidate will have a balance of formal education and industry experience
* Holding an advanced degree in Pharmaceutical Sciences.
* 10+ years of relevant experience in a regulatory affairs management role.
* Strong oral and written English language skills.
* Proven leadership, network building and team player skills.
* Excellent communication, negotiation and interpersonal skills.
* Be a self-starter and whilst remaining focused on strategic goals, possess the ability to multi-task and work to agreed timelines.

To apply:
If you would like to discuss this vacancy further, please call Alisha Nandhe on +44 (0)20 3326 4123, or email anandhe@i-pharmconsulting.com. If this role is not suitable, Alisha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


About i-Pharm

i-Pharm Regulatory is a specialist Recruitment team working wholly within the Regulatory Affairs market. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm Regulatory is a team within the larger organisation i-Pharm Consulting which provides candidates in areas such as: Clinical Operations, Pharmacovigilance, Biometrics, Project Managements, Quality Assurance and Health Economics. Visit our website to see our extensive current vacancies:

www.i-pharmconsulting.com

Keywords:

Regulatory Affairs / Reg Affairs / RA / Regulatory Affairs Officer / Reg Affairs Officer / RA Officer / systems / variations / dossier / labelling / registrations / renewals / submissions / CMC / Central Europe / Belgium / Brussels / Antwerp

Apply for this job: Regulatory Affairs Associate Director

Contact Information:

Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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