The QA Manager will be responsible for driving a continuous Quality Assurance and Compliance improvement mindset within the operations. This role requires providing strategic leadership and project management of Quality Assurance to ensure compliance with applicable regulatory requirements.
Responsibilities:
- Drive a continuous Quality Assurance and Compliance improvement mind-set within the operations.
- Provide QA strategic leadership and project management of Quality Assurance ensuring compliance to applicable regulatory requirements and in co-operation with all relevant functions. The responsibility covers QA GMP activities: QA Infrastructure, Sterility Assurance, Quality Systems, ...
- Lead the quality related activities at the site to ensure safe, efficacious, and quality product can be supplied in accordance with regulatory and business requirements.
- Responsible for the leadership and operational quality management.
- Manage and supervise all activities related to product quality in the Company and ensure that these activities comply with WHO GMP, Com. GMP and regulation of the Ministry of Health of Vietnam.
- Co-ordinate others manager to resolve problems that concern with product quality.
- Co-ordinate the work of Quality Assurance Department.
- Approve or reject intermediate product, the products are waiting packaging and finished – product according to the Company’s Policy.
- Review batch records and approve for release when ensuring that all product batches are manufactured in compliance with GMP regulations and meet requirements of registered according to the Company’s Policy.
- Review Validation Master Plan and ensure implementation of validation / calibration, training, and self-inspection program.
- Organize or participate annual GMP, GLP, GSP self-inspections and prepare corrective action plan.
- Manage Quality Assurance operation to achieve annual departmental target and budget.
- Prepare suitable objectives for QA staffs and carry annual performance appraisal.
- Take part in training GMP, Quality Management System.
- Take part in assessing the suppliers.
- Hold quality meeting frequently.
- Co-ordinate with RA Department to prepare registration documents according to RA’s requirements.
