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Regulatory Affairs Specialist Residues

Employer
Thornshaw Recruitment
Location
Dublin (City), Leinster (IE)
Salary
Negotiable
Start date
5 Oct 2020
Closing date
4 Nov 2020

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Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

On behalf of my client, a company specialising in the development and registration of plant protection products, we are now looking to fill  a new vacancy for a  Senior Regulatory Specialist in Residues and Analytical Methods.  This is a new opportunity in their regulatory team for an experienced regulatory affairs professional who wishes to put their knowledge and training to use in a fast-paced, results-focused commercial R&D environment. Although the role will focus on residues and analytical methods, there will also be opportunities to gain exposure and training in other dossier sections. 


Key Responsibilities:


•    Summarising data relating to analytical methods for pesticides in different matrices (soil, air, water, crops etc.) 
•    Preparing position papers and higher tier refinements to support residue risk assessment 
•    Conducting dietary risk assessments for humans and livestock 
•    Design and troubleshooting of residue trials, metabolism studies and analytical methods supporting these studies 
•    Data gap analysis for active substances and products 
•    Preparation and review of draft registration reports, with a particular emphasis on residues and analytical methods sections 
•    Develop strategies to gather new data 
•    Liaison with Member State regulatory authorities, consultants, CROs, test facilities and other internal departments (e.g. 
laboratory) 
 


Experience/Qualifications:

•    Excellent academic record in a relevant scientific subject (analytical chemistry or related disciplines). A degree is essential, with a masters or PhD being an advantage 
•    2-3 years of experience in regulatory affairs, preferably with some specialisation in residue chemistry 
•    Ability to present clear and concise written arguments to support a specific regulatory or scientific position on a topic 
•    Ability to come up with new ideas and creative solutions 
•    Excellent attention to detail is a must 
•    Ability to work on own initiative or as part of a team, in meeting strict timelines 
•    Excellent organisational skills with the ability to multi-task and work in an environment with shifting priorities 
•    Performance driven, with a 'can-do' attitude 
•    Proficiency in Microsoft Word, Excel, PowerPoint. 

For full details please contact Tina at +353 1 2784672 or email your CV to tdunne@thornshaw.com
Thornshaw Scientific is a division of the CPL Group www.thornshaw.com

Company

thornshaw-title

Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment.  In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.

Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.

Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.

Our Industries

We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years. 

Our Specialities

Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.

Our Mission

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For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com

 

Company info
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