This is an excellent opportunity for an experienced Regulatory Affairs professional to join a leading, global veterinary pharmaceutical company based in Northamptonshire. This role will allow you the chance to expand your skillset within Regulatory Affairs and Quality with an established, market leading organisation by ensuring product compliance with relevant directives, regulations and other legislation, along with other administrative duties.
Ensure products are compliant with relevant directives, regulations and other legislation. Liaise with relevant bodies/ authorities, managing the response to questions in respect of UK and Irish submissions to agreed deadlines.
Ensure information related to Regulatory Submissions and Regulatory Approvals is circulated to the appropriate personnel/ departments.
Assist the Regulatory Affairs Manager with the submissions of variations.
Ensure up-to-date datasheets for NOAH and the Animal and Plant Health Agency (APHA) are completed following new product introduction and variations.
Provide support in documenting and filing complaints in the Company’s quality complaints system and assist in any delegated administrative tasks for the quality department
Responsible for the timely preparation and submission (where relevant) of the Company’s regulatory documentation, including Product Quality Reviews(PQR’s), Product Master Files and Anti-microbial returns (AMRs).
Previous experience with Regulatory Affairs within veterinary pharmaceutical industry essential
Good knowledge of veterinary pharmaceutical regulations and governing bodies
Strong communication skills and organisation is essential
If you are interested in the above role then please apply or get in touch to discuss further.
Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.