23 Jun

Head Regulatory Affairs Jobs Vacancy in Luxembourg Medicine Ltd

Position
Head Regulatory Affairs
Company
Luxembourg Medicine Ltd
Location
Opening
23 Jun, 2018 24 days ago

Luxembourg Medicine Ltd urgently required following position for Head Regulatory Affairs. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.

Follow the online directions, complete all the necessary fields, and provide all relevant information so your application is submitted correctly. When you click the 'Apply this Job' button (open in new window) you will be taken to the online application form. Here you will be asked to provide personal and contact details, respond to employment-related questions, and show how you meet the key selection criteria.

Head Regulatory Affairs Jobs Vacancy in Luxembourg Medicine Ltd Jobs Details:

Luxembourg Medicine Company Limited, owner of the renowned brand names Madame Pearls(珮夫人) and Pearls (珮氏), has been operating in Hong Kong since 1954. Our company engaged in the manufacturing and sales of medicinal and healthcare products with a heritage of over 50 years.

Responsibilities:
Ensure drug registration activities are proceeded in accordance with relevant local, mainland China and overseas regulations and develop the strategy to obtain the product approval within target timeframe;

Provide overall regulatory guidance towards execution;

Monitor and communicate within the company for the current and proposed changes on drug registration dossiers to ensure all the operations within company relating to product registration comply with the regulatory requirements and business needs;

Supervise and monitor all supporting activities relating to drug regulatory requirements are proceeded according to schedule.

Requirements:
University graduate major in Science or medical related discipline;

8 years regulatory affairs experience in pharmaceutical industry is preferred;

Good working knowledge and experience on local, mainland China and overseas drug regulatory requirements;

Strong interpersonal and communication skills;

Detail-oriented and cross-functional team player;

Proficiency in written and spoken English Chinese including Mandarin.

Interested parties please send full resume with present and expected salary to Human Resources Department by clicking "APPLY NOW".

(Information provided will be treated in strict confidence and will only be used for recruitment-related purposes.) Full-time


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