The Position
As a Qualified Person at Novo Nordisk, you will be a QP in a team that releasing clinical trial products and marketed products according to relevant MoH requirements and regulations. You will work closely with the Clinical Trials team and Commercial Supply Chain department to ensure product quality and timely release.
Your will also:
Handle processes such as deviations, repackaging, and import of non-registered products and update quality agreements and SOPs.
Follow up on the implementation of updated packaging materials and leaflets for marketed products.
Work with various computerized systems.
Review APRs and handle temperature deviations reports during storage of registered/marketed products.
Collaborate with internal and external stakeholders.
About the Department
The QP team in Novo Nordisk Israel is managed by QP and PV Senior Manager and is responsible on releasing products to the market and for clinical trial products.
QP team is part of CMR unit that includes Clinical, Medical and Regulatory teams as well.
Qualifications
To be successful in this role, we are looking for candidates with pharmacist license from the MoH (B.Sc Pharm degree) as a mandatory request. QP authorization by the MoH or compliance with the MoH threshold mandatory.
Strong understanding of MoH requirements and regulations.
Experience in release of tablets and sterile products advantage.
Experience in issue quality agreements and SOPs.
Experience in handling temperature deviations in storage and distribution level.
Fluent in Hebrew and English
As a person, you are a responsible individual with a strong work ethic. Your ability to collaborate effectively in teams and work independently makes you a versatile asset. Coupled with your eagerness to learn, you are a quick-thinking problem-solver who can make informed decisions with precision and organization. Your proficiency in computer skills further enhances your ability to tackle challenges efficiently.
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