SonicJobs Logo
Login
BackBack to search

Senior Manager Regulatory Affairs & Pharmacovigilance

Qube Recruitment
Posted 23 days ago, valid for 10 days
Location

Dartford, Kent DA1 1BG, England

Salary

£60,000 - £80,000 per annum

info
Contract type

Full Time

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

Sonic Summary

info
  • Salary: Not specified
  • Experience required: Minimum 10 years plus in Regulatory Affairs of Medicines, Food supplements, and Cosmetics
  • Define, develop, and lead regional strategies for regulatory and pharmacovigilance success
  • Oversight of a team of 4 to ensure daily activities in Regulatory and Pharmacovigilance are carried out
  • Represent the company with regulatory agencies across the UK and EU

Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit aSenior Manager Regulatory Affairs & Pharmacovigilance.

Job Requirements:

Define, develop, and leads regional strategies to maximise regulatory and pharmacovigilance success. Effectively communicate the likelihood of pros and cons to Management.

  • Sound knowledge on requirements of MA Transfer in EU territories, which includes requirements of notarisations and translations.
  • Oversight a team of 4 to ensure day to day activities are carried out in Regulatory and Pharmacovigilance.
  • Sound Knowledge of requirements of Minor and Major complex Variations.
  • Ensure that CMC practices are carried out in accordance with the requirements of regulatory bodies.
  • Responsible for reviewing and signing off bio-waiver declarations and quality overall summaries.
  • Support and carry out the Risk Assessments process as required by the business.
  • Provide oversight for the development and maintenance systems to ensure and support Regulatory and Pharmacovigilance compliance requirements are met.
  • Always assure inspection preparedness to support overall corporate strategy.
  • Ensure that procedures are in place and followed for effective working of the regulatory and pharmacovigilance department.
  • Provide organisation with strategic advice for the launch of new products in EU & UK.
  • Responsible for reviewing and signing off the agreements with external contactors.

Representing the company with regulatory agencies across UK & EU

  • Monitoring and setting timelines for the team of individuals to meet the deadlines.
  • Monitoring and setting timelines for licence variations and renewal approvals.

Qualifications and Experience (as applicable):

  • Educated to degree level in science or equivalent experience.
  • Minimum 10 years plus of experience in the Regulatory Affairs of Medicines, Food supplements and Cosmetics
  • Proficiency in the use of MS Office suite (Excel, PowerPoint)
  • Ability to take initiative and work with different departments as a team player within the organisation.

Monday to Friday: Full Time

Apply now in a few quick clicks

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.