
Job Description
Job Description:
Mastery of Quality Management Systems (QMS), GMP and GDP
Mastery of Deviation, CAPA, Change Control, Risk Assessment and Complaint Handling
Mastery of SOP and protocol documentation and writing
Familiarity with the principles of Quality Risk Management (QRM)
Mastery of document management systems, continuous improvement and analysis of quality indicators, implementation of quality improvement projects and submission of periodic reports to the organization's senior management
Supervision and control of SMF, VMP, CTD, DMF documentation
Supervision, monitoring and review of production information and product quality control
Participation in the validation of water and air conditioning systems in various production departments and clean rooms
Ability to plan and implement internal and external audits
Compile, review and control documentation, implementation methods and quality guidelines
Eligibility requirements:
At least 8 years of experience in quality assurance management in the pharmaceutical and supplement industries
Leadership and team management skills
Decision-making and problem-solving abilities
Communication and negotiation skills Effective
English proficiency
Employment Type
Job Category
Educations
Seniority
Details
Employment type
Job Category
Educations
Seniority
