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Regulatory Affairs - Executive

2.00 to 3.00 Years   Ahmedabad (Gujarat)   08 Apr, 2019
Job LocationAhmedabad (Gujarat)
EducationAny Graduate
SalaryAs per Industry Standards
IndustryManufacturing/Industrial
Functional AreaBio Tech/R&D/Scientist
EmploymentTypeFull-time

Job Description

  • B.Pharm, M.Phar, M.sc., B.sc., Bio-Medical Engineer with 2-3 years of experience in Q.A. of Pharma / Medical Device companies. Candidates withe experience in Medical Device company will be preferred.
  • 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
  • Keyskills :
    Regulatory Affairs - ExecutiveB.PharmM.PharBio-Medical EngineerHealthcare products Regulatory

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