Responsibilities:

• Report to the Head of Regulatory Affairs.
• Assist in coordination between R&D / RA and GMP site to assure that all pharmaceutical products are developed and registered in compliance with company’s policy and statutory requirements.
• Participate in product development and technology transfer projects, and regulatory affairs activities.
• Assist in continuous improvement of the Pharmaceutical Quality System (PQS) and GxP processes.
• Upgrade the Pharmacovigilance / Adverse Drug Reaction (ADR) system.
• Handling of Dangerous Drugs.
• Assist ad-hoc projects as assigned by the Management.

Requirements:

• A holder of bachelor degree or above in Pharmacy.
• Must be a Registered Pharmacist with a valid practicing certificate in Hong Kong.
• Preferably with knowledge and experience in pharmaceutical development, PIC/S GMP and drug safety.
• Good interpersonal and communication skills.
• Good command of written and spoken English and Chinese.
• This post must be occupied by a full-time personnel.
• Immediate available is highly preferred.

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.