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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

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. ...


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 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:


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
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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