Responsibilities:

• To ensure and maintain the adequate and accurate records for controlling and monitoring conformity to specified GMP and statutory requirements
• To perform the routine and ad-hoc functions of Production Department
• Prepare and maintain the quality documentation system, including the standard operation procedures (SOPs), specifications and protocols
• Participate in the routine-in-process control in production department

Requirements:

• Higher Diploma or above in Pharmaceutical Studies or Science related discipline. Fresh graduate will also be considered
• Have good knowledge in GMP standard, auditing documentation and report writing skills
• Knowledge in pharmaceutical production equipment and HK GMP System is a definite advantage
• Attention to details, hard working and being able to work under pressure
• Strong communication skill with good command of English and Chinese

Please send detailed resume with salary expected by email t.tsang@qplab.com.hk

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