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Regulatory Affairs Advisor

King's Lynn, Norfolk

£350 - £385 per day

Contract (Part time)

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Are you an experienced Regulatory Affairs Professional with knowledge and experience within the Pharmaceutical and Medical Device sector, excellent communication skills and a drive for customer focus?

  • If so, we have an excellent opportunity for an experienced Regulatory Affairs Professional to join our team on a contract basis working 1 to 2 days per week.

  • As our new Regulatory Affairs Advisor, we are looking for you to complete, maintain, own and deliver all regulatory documents, e.g. MHRA licences, DMF etc.
    Your role will be to provide specialist advice and information of regulatory and licensing procedures throughout the company and to support and advise on the regulatory submissions; coordinating, maintaining and submitting the regulatory files (DMF, 510(k), technical files, MAF, site master file).

  • Key Skills & Experience
    *Educated to degree level.
    *Working knowledge and experience of regulatory submissions.
    *Knowledge of pharmaceutical and drug licensing processes, guidelines and legislation.
    *Able to work as part of a wider team.
    *Excellent organisational skills; managing time and adapting when necessary.
    *Experienced user of business computer systems and software.
    *Good communication and interpersonal skills.

  • Desirable Skills & Experience
    *Experience in EU & USA Regulatory Filing processes for Medicines and Medical Devices.
    *SAP user.

  • Orion Electrotech Ltd acts as both an Employment Business and Employment Agency and complies with the Conduct of Employment Agencies and Employment Businesses Regulations Act 2003.

  • By applying for this position please take a few moments to view our Privacy Notice on our Orion website which details how we retain and process your data. Alternatively please give us a call so we can discuss this with you.

Posted 133 days ago

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