Global Regulatory Leads

6 days left

Location
Remote Based, with travel requirements to Lancashire/North Yorkshire office when required
Salary
Competitive
Posted
09 Feb 2021
Closes
11 Mar 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Do you want to be part of a fast-growing, globally recognised scientific and regulatory company?

If you do, we want to hear from you as we have a number of exciting regulatory roles within our growing team.

Global Regulatory Leads wanted in Clinical, Non-clinical and Quality to cover Medical and consumer product regulations.

As BNS ramps up its Regulatory Affairs capabilities, we are seeking applicants with around 5-10 years industry experience in designing strategic approaches and delivering product submissions to global regulatory agencies with specialisations in any of the above disciplines.

Main Purpose of job

Broughton Nicotine Services are a contract research organisation providing analytical, scientific, and regulatory support to businesses in the e-cigarette and other sectors which cover both consumer products and medical products to be used for nicotine replacement therapy enabling them to increase the value of their business and advance a smoke-free future.

As BNS in-house subject matter expert on regulations relating to CMC/Quality, non-clinical, clinical or medical device requirements for nicotine and non-nicotine projects whether for a commercial or a medical indication, you will advise clients on the particular requirements for their products and work with the pharmaceutical development and other departments in BNS to ensure that these requirements are delivered either pre submission or in life cycle management.

  • Graduate degree in science
  • 5 years experience in CMC/Quality Regulatory Affairs
  • Experience of interaction with Regulatory agencies e.g. FDA, MHRA, EMA
  • Formal Regulatory Affairs professional qualifications preferred
  • Pharmaceutical or tobacco industry experience

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