i-Pharm Consulting

Regulatory Affairs Manager

Location
Netherlands
Salary
Negotiable
Posted
04 Dec 2018
Closes
18 Dec 2018
Ref
RAMCMC - TJ1
Contract Type
Permanent
Regulatory Affairs Manager, Netherlands

An exciting Pharma/Biotech is looking for an experienced RA Manager to join their growing RA department in the Netherlands. If you are an RA Manager with 5+ years’ experience in overseeing, supporting and reviewing the RA processes within pharmaceuticals and biotech, this is the perfect opportunity for you!

Job Title: Regulatory Affairs Manager
Location: Netherlands

Type of Contract: Permanent

Compensation: Very Competitive Salary + Benefits

Job Responsibilities:

* Working as a core member of regulatory team
* Point of contact for Regulatory Affairs
* Manage a team of RA professionals
* Support for situations involving regulatory matters
* Create and submit dossiers for new countries and products as required
* Prepare company for major regulatory legislation changes within the country

Ideal Candidate:

* 5+ years of regulatory affairs experience
* Dutch and English Proficiency
* Knowledge of Biotechnology is advantageous
* CMC experience

To apply:
If you would like to discuss this vacancy further, please call Tom Jackman on +44 (0)20 3198 0490, or email tjackman@i-pharmconsulting.com. If this role is not suitable, Tom 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 / Netherlands/ Utrecht / Rotterdam / Haarlem / Amsterdam

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