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senior regional manager, group regulatory affairs.

job details

summary

    job details

    We are currently looking for a regional manager under group regulatory affairs for one of the largest medical device manufacturers in the world, with a legacy of over 50 years internationally.

    • Reporting to: Regional Director, Group Regulatory Affairs
    • Location: Subang Jaya, Selangor
    • Managing a team of 16 people
    • Excellent employee compensation and benefits

    the role
    • Managing the entire process for regulatory approval of medical products.
    • Ensure all registration documents complying with the local standards for submission.
    • Supervising the RA personnel performance, to ensure all the activities and projects are carried out in a timely manner.
    • Demonstrate excellent stakeholder management, including regulatory evaluators.
    • Provide regulatory support for all products to the team.


    the experience

    • 5+ years of professional experience in the field of medical devices and regulatory affairs relating to medical devices.
    • A university degree in any scientific discipline.
    • Skilled in analysing information, technical understanding, promoting regulatory awareness, managing processes & problem solving.


    how to apply

    To apply online, please click on the appropriate link. Alternatively, please contact Shash at 0129175705 or drop an email to shash.prasanan@randstad.com.my if you are interested in the job.

    We are currently looking for a regional manager under group regulatory affairs for one of the largest medical device manufacturers in the world, with a legacy of over 50 years internationally.

    • Reporting to: Regional Director, Group Regulatory Affairs
    • Location: Subang Jaya, Selangor
    • Managing a team of 16 people
    • Excellent employee compensation and benefits

    the role
    • Managing the entire process for regulatory approval of medical products.
    • Ensure all registration documents complying with the local standards for submission.
    • Supervising the RA personnel performance, to ensure all the activities and projects are carried out in a timely manner.
    • Demonstrate excellent stakeholder management, including regulatory evaluators.
    • Provide regulatory support for all products to the team.


    the experience

    • 5+ years of professional experience in the field of medical devices and regulatory affairs relating to medical devices.
    • A university degree in any scientific discipline.
    • Skilled in analysing information, technical understanding, promoting regulatory awareness, managing processes & problem solving.


    how to apply

    To apply online, please click on the appropriate link. Alternatively, please contact Shash at 0129175705 or drop an email to shash.prasanan@randstad.com.my if you are interested in the job.