Main PurposeTo primarily be the Quality leader for the MDI Pharmaceutical operation at the site with overall responsibility for the quality of activities performed and materials produced in the MDI facility including line management of the quality control and quality assurance functions. To provide specialist knowledge, expertise and input related to quality assurance, regulatory compliance, cGMP, systems, processes and procedures for medical propellants and MDI business globally. To deploy personal competence and QA / QC experience to deliver customer support to internal and external customers, specific assigned projects and to support new pharma business initiatives.Main Responsibilities
- Plan and coordinate QC laboratory and QA activities for agreed development projects.
- Supervise QC laboratory and Quality Assurance resources to execute projects within allotted budget and timelines.
- Ensure Quality procedures comply with required quality and safety standards and if necessary, develop procedures, experimental protocols and work instructions.
- Ensure QC test results and experimental data are provided to agreed schedules.
- Produce timely and accurate technical and management reports for presentation to management and customers.
- Review and recommend improvements to facility procedures, techniques and technologies.
- Identify and recommend training to team members when needed.
- Enforce company policies and safety regulation...