Responsibilities:
To support in developing, implementing and maintaining the documentation and quality assurance system of the company, including the standard operating procedures (SOPs);
To ensure the adequate records are maintained for controlling and monitoring conformity to specified GMP and statutory requirements;
To support the routine QA Department functions, including GMP training, self-inspection, line clearance;
Knowledge in Quality Management System (e.g change control, risk assessment and CAPA) is an advantage.
Requirements:
Higher Diploma or University graduate in Pharmaceutical Studies / Food science/science related discipline;
Attention to details, hard-working and being able to work under pressure;
Strong communication skill, good command of English and Chinese;
Minimum of 1 year relevant experience;
Experience in pharmaceutical industry is an advantage;
We offer attractive remuneration package including medical scheme, discretionary year-end bonus etc. Interested parties please send full resume with salary expectation and availability by click "Apply Now". Only shortlisted candidates will be interviewed.
Synco (H.K.) Ltd is an Equal Opportunities Employer. Personal data provided by job applicants will be used strictly in accordance with our personal data policy and for recruitment purposes only. We aim to respond to successful applicants within 8 weeks and related information will be kept in our file for up to 12 months for other suitable vacancies in our organization and thereafter destroyed.
Full-time,Permanent
举报职位
