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Regulatory Affairs Manager

Reed
Posted a day ago, valid for 8 days
Location

Runcorn, Cheshire WA7 2FG, England

Salary

£50,000 - £60,000 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The Head of Regulatory Affairs position is located in the North-West of the UK and is a full-time, permanent role requiring onsite work 3-4 days per week.
  • The successful candidate will oversee the regulatory affairs team, develop regulatory strategies, and ensure compliance with current legislation.
  • Candidates should have proven experience in regulatory affairs within the pharmaceutical or medical device industry, along with strong leadership and team management skills.
  • The role includes responsibilities such as managing regulatory submissions, maintaining licenses, and overseeing local regulatory budgets.
  • The salary for this position is competitive, and candidates are expected to have significant experience in the field.

Head of Regulatory Affairs (Healthcare)

Location: North-West, UK

Full time & permanent position

Onsite 3-4 days per week

Reed Scientific are working with a global healthcare provider based in the North West of the UK, and are currently seeking an experienced Regulatory Affairs Manager to oversee and manage the regulatory affairs team.

Main Responsibilities:

  • Regulatory Strategy: Develop and implement regulatory strategies aligned with the companies’ strategic objectives
  • Team Leadership: Lead, support, and develop the regulatory affairs team
  • Regulatory Submissions: Oversee the filing and approval of regulatory submissions for licensed and unlicensed products
  • Compliance: Ensure promotional materials, product labelling, and regulatory submissions comply with current legislation and guidelines.
  • Budget Management: Agree and review local regulatory budgets
  • License Maintenance: Ensure all licenses, including specials licenses, are up to date.
  • Resource Management: Manage resourcing requirements within the regulatory affairs team.

Skills & experience:

  • Proven experience in regulatory affairs within the pharmaceutical or medical device industry.
  • Strong leadership and team management skills.
  • Excellent knowledge of regulatory requirements and guidelines.
  • Ability to develop and implement effective regulatory strategies.
  • Strong communication and interpersonal skills.

If this looks like a position of interest and you possess the required skills and experience then please follow the link to apply.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.