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Junior Regulatory Affairs Officer

SKC Recruitment Ltd
Posted 6 hours ago, valid for 22 days
Location

Leicester, Leicestershire LE1 4PG, England

Salary

£24,000 - £27,000 per annum

Contract type

Full Time

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Sonic Summary

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  • The role of Junior Regulatory Affairs Officer involves supporting Parallel Trade, Regulatory Affairs, and Quality Management within a pharmaceutical organization.
  • Candidates should have experience in Regulatory Affairs and Parallel Trade, along with a strong understanding of the pharmaceutical industry and its products.
  • Key responsibilities include submitting licenses, collaborating with various teams, maintaining licenses in the Quality Management System, and identifying regulatory risks.
  • The position requires strong communication, teamwork skills, and proficiency in Excel and data analysis tools.
  • The salary for this position is competitive, and candidates are expected to have at least 1-2 years of relevant experience.

Role: Junior Regulatory Affairs Officer

Oue client is looking for a Junior Regulatory Affairs Officerto join theirteam to support all aspects of Parallel Trade (PLPI), Regulatory Affairs, and Quality Management. You will work closely with the Regulatory Affairs Lead and Senior Specialists to ensure high standards in implementing Quality and Regulatory strategies, adhering to MHRA guidelines.

Key Responsibilities:

  • Submit and implement new licenses/variations promptly.
  • Collaborate with MHRA, Quadrant License Teams, and Pharmagen to ensure smooth production processes.
  • Maintain licenses within the Quality Management System.
  • Stay updated on training, processes, and regulations.
  • Identify and escalate regulatory risks.
  • Process license applications to minimize MHRA RFIs.
  • Support Pharmagen Production and Quality Departments.

Experience:

  • Experience in Regulatory Affairs and Parallel Trade.
  • Deep understanding of the pharmaceutical industry and its products.
  • Expertise in Quality Management Systems, Deviations, Change Controls, Risk Assessments, Validations, and MHRA Systems.
  • Organized, proactive, and commercially aware.
  • Strong communication and teamwork skills.
  • Flexible, creative, and a problem solver with analytical abilities.
  • Proficient in Excel, data analysis, and decision-making tools.
  • Knowledge of patents and trademark legislations
  • Project management experience.

Please apply if you are looking for a remote role within a growing pharmaceutical organisation.

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