Assistant Officer – Quality & Regulatory Affairs

Responsibilities

• Assist to perform and maintain QA activities and records for product release, product return and repackaging to ensure the compliance of GMP, GDP, and regulatory requirements
• Assist to coordinate and execute process validation; prepare documentations, policy, protocol and report
• Assist in establishing and maintaining quality management system and an efficient pharmacovigilance system in compliance with the local authority’s regulation and Regional PV policies & SOPs
• Provide support in the GMP (repackaging) operation including incoming materials inspection, in process control and finish product sampling
• Support regulatory affairs/ product registration related activities
• Process documentation of corrective actions plans and monitors implementation;
• Participate ad hoc project as assigned

Job Requirements

• Bachelor degree or above in related scientific discipline
• 1-2 years of relevant QA experience in food/healthcare products/ pharmaceutical industry is preferred;
• Knowledge in ISO, GDP, GMP and QMS is an advantage
• Strong team player, can-do attitude, detail minded, eager to learn, high self-driven to exceed expectations and take up more challenges
• Good command of both written and spoken English and Chinese, including Mandarin

If you have the energy and qualifications to add to our velocity, Please visit KLN Company Webpageto apply or send your CV with your present and expected salary to Human Resources & Administration Department by clicking Apply .

We are an equal opportunity employer and welcomes applications from all qualified candidates. All personal data will be kept in the strictest confidence and will be used for recruitment purpose only. All applicants maybe considered for other suitable positions in KLN Logistics Group. All personal data of unsuccessful candidates will be destroyed.