Category
Regulatory, Quality and Clinical
Description
Responsibilities
- Drive the design and equipment procurement in the establishment of a new analytical laboratory
- Establishment of test methods by technology transfer from head office and in house development
- Establish and manage external contract testing capabilities
- Manage the qualification of all equipment and the validation of test methods.
- Prepare new Quality Documents and revision/update of existing documents within the ownership of the QC group.
- Hire, train and mentor QC and analytical staff
- Manage rostering to ensure continuity of service up to two shifts and 7 days
- Run and participate in risk assessments, internal audits and quality investigations relevant to area of responsibility or expertise.
- Manage the sampling and testing of intermediates or products.
- Manage the sampling and testing of chemicals and raw materials for release, including pharmaceutical water testing
- Manage calibration and maintenance activities for all quality control equipment in line with documented schedules
- Maintain quality control testing records and data entry ensuring industry standard data integrity principles are maintained.
- Establish and maintain a stability testing program for products and intermediates in compliance with ICH guidelines.
- Preparation of specifications for testing of materials and products
- Overall responsibility for the environmental monitoring program