Senior Executive Regulatory Affairs Job in Poly Medicure Limited

Senior Executive Regulatory Affairs

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Job Summary

Job Description

The ideal candidate will be responsible for driving the company's key performance indicators by delivering an exceptional in Regulatory affairs with knowledge of well established technologies & legacy products.


Responsibilities:

  • Sound knowledge and understanding of EU procedures MDD, MDR, MDCG, CER and MEDDEV papers
  • Sterilization procedures and respective validation
  • Clinical Evaluation report writing/proof-reading
  • Hands on Experience in and management as per EN ISO 14971
  • Processing of incident reports (MIR format of EU)
  • Independent creation and maintenance of technical documentation as per MDD and MDR
  • Purchase and delivery specifications
  • Preparation for international products approvals (registrations)
  • Define and support CAPA in the common interface between second party and Polymed
  • verification planning for development projects
  • Supervision/adoption of test methods according to international norms
  • Support to second party audit team during annual assessment certification body.
  • Conversation to the client and Quality checks of models, drawings & assembles according to client standard & their checklists

Qualification & Experience:

  • Bachelor of Technology in Mechanical Engineering / M.Sc. in Medical Technical Engineer, Pharmacy, Healthcare Technology
  • 4 to 6 years experience in MD RA and EU MDD
  • Sound experience in single use MDs, class I-III
  • Strong verbal or written communication skills


Qualification :
B.Tech/B.E. in Mechanical
Experience Required :

2 to 6 Years

Vacancy :

2 - 4 Hires

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