Jobs Career Advice Signup
X

Send this job to a friend

X

Did you notice an error or suspect this job is scam? Tell us.

  • Posted: Feb 20, 2019
    Deadline: Not specified
    • @gmail.com
    • @yahoo.com
    • @outlook.com
  • Never pay for any CBT, test or assessment as part of any recruitment process. When in doubt, contact us

    Roche was one of the first companies to bring targeted treatments to patients. With our combined strength in pharmaceuticals and diagnostics, we are better equipped than any other company to further drive personalised healthcare. Two-thirds of our Research and Development projects are being developed with companion diagnostics. We are the world's number 1 i...
    Read more about this company

     

    Regulatory Affairs and Quality Assurance Manager

    Job Description

    • We are seeking a Regulatory Affairs and Quality Assurance Manager in Lagos, Nigeria to manage the Regulatory Affairs and Quality Assurance functions for Roche Diagnostics in the West Africa territory (Nigeria and Ghana) and support the export distributors and marketing and sales colleagues.
    • The role would involve working closely with the Country Manager, Nigeria with regards to regulatory affairs and quality assurance related projects.
    • This role will also serve to assist the Head of Regulatory as the Deputy Local Safety Officer, and coordinator for the West Africa distributor certification and improvement in line with ISO standards.

    Responsibilities
    The overall objective of this role is to oversee the Regulatory and Quality Affairs for Nigeria and Ghana as directed by management. These include but are not limited to:

    • Ensuring the timely preparation of organized and scientifically valid domestic and international product submissions.
    • Initiating / completing all product registration activities as assigned within defined timeframe.
    • Cultivating and fostering good relationships with all relevant Regulatory organizations (NAFDAC and GHANA-FDA) within assigned territories.
    • Submitting weekly plans, monthly activity reports and quarterly reviews to the Head of Regulatory.
    • Adhering to corporate principles and exercises policies conforming to Roche values and realize agreed Management Center, Sub regional and Regional Diagnostics programs and objectives.
    • Driving high performance culture and cultivates entrepreneurial spirit.
    • Taking the lead in ensuring Good Lab Practice by all Roche partners and stakeholders.
    • Ensuring timely reporting of all Quality related / Product Complaint issues according to Roche SOP’s.
    • Monitoring of dissemination of all Safety Board notices (SBN’s) and Quality Notifications (QN’s).
    • Training and monitoring of Roche partners and customers as required on Temperature Monitoring Devices (TMD) use and reporting / downloading.

    Requirements
    You, as an ideal candidate, will have the following skills, experience and education:

    • Medical/ Science degree e.g. Lab Science / Pharma background.
    • 4 - 6 years’ work experience in Nigeria; additional experience in Ghana would be an advantage.
    • Minimum of 2 years’ experience in Medical Devices / Pharma Regulatory Affairs
    • Advanced Computer Literacy in MS Office.

    Method of Application

    Interested and qualified? Go to Roche on roche.wd3.myworkdayjobs.com to apply

    Build your CV for free. Download in different templates.

  • Send your application

    View All Vacancies at Roche Back To Home

Subscribe to Job Alert

 

Join our happy subscribers

 
 
Send your application through

GmailGmail YahoomailYahoomail