i-Pharm Consulting

Regulatory Affairs Consultant

Location
Belgium
Salary
Negotiable
Posted
02 Jan 2019
Closes
16 Jan 2019
Ref
14145 - TJ
Contract Type
Contract
Regulatory Affairs Consultant

An amazing opportunity to work within the Regulatory Affairs department of a Leading Global Life Sciences Company has become available. You will be working at a Consultant level, overseeing the regulatory strategy for a portfolio of products.

Job Title: Regulatory Affairs Consultant
Location: Belgium

Contract / Freelance position - Homebased

Contract Length: 8 Months – 1FTE

Job Responsibilities:

* Maintain and update existing regulatory authorisations
* Provide guidance and coaching to lower level team members
* Obtain and maintain Marketing Authorisations for a portfolio of products
* Implement complex regulatory strategies
* Serve as a consultant to Managers
* Compile and submit regulatory documents according to requirements within a deadline

Ideal Candidate:

* 4+ years of regulatory or comparable experience within a pharmaceutical company, CRO, or similar organization.
* Broad Regulatory Submissions Experience, including: MAAs, Variations, Renewals etc.
* CMC experience preferred
* Education up to bachelor’s degree or country equivalent in pharmacy/related discipline.
* PhD/Higher degree is not required but is an advantage.
* Fluent in English, any other languages are bonus


To apply:
If you would like to discuss this vacancy further, please call Tom Jackman on +44 (0)20 3189 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 / Belgium / Brussels / Antwerp / Wavre / Charleroi

Similar jobs

Similar jobs