SE

Regulatory Affairs Manager

Seven Consultancy
Kolkata3-6 LPA Posted 18 Dec 2025
FULL TIME
labelling
Documentation
Negotiations

Job Description

  • Studying scientific and legal documents

  • Gathering, evaluating, organising, managing and collating information in a variety of formats

  • Ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency (MHRA)

  • Maintaining familiarity with company product ranges

  • Planning, undertaking and overseeing product trials and regulatory inspections

  • Keeping up to date with changes in regulatory legislation and guidelines

  • Analysing complicated information, including trial data

  • Offering advice about company policies, practices and systems

  • Obtaining marketing permission

  • Outlining requirements for labelling, storage and packaging

  • Using a variety of specialist computer applications

  • Liaising and negotiating with regulatory authorities

  • Providing advice about regulations to manufacturers/scientists

  • Writing comprehensible, user-friendly, clear product information leaflets and labels

  • Ensuring that quality standards are met and submissions meet strict deadlines
Join WhatsApp Channel